| Name |
|---|
COQ10B Genecoenzyme Q10 homolog B (S. cerevisiae) Predicted to enable ubiquinone binding activity. Predicted to be involved in cellular respiration. Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
COQ10A Genecoenzyme Q10 homolog A (S. cerevisiae) Predicted to enable ubiquinone binding activity. Predicted to be involved in cellular respiration. Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
COQ10BP2 Genecoenzyme Q10 homolog B pseudogene 2 |
COQ10BP1 Genecoenzyme Q10 homolog B pseudogene 1 |
MMAA Genemethylmalonic aciduria (cobalamin deficiency) cblA type The protein encoded by this gene is involved in the translocation of cobalamin into the mitochondrion, where it is used in the final steps of adenosylcobalamin synthesis. Adenosylcobalamin is a coenzyme required for the activity of methylmalonyl-CoA mutase. Defects in this gene are a cause of methylmalonic aciduria. [provided by RefSeq, Jul 2008] |
MMAB Genemethylmalonic aciduria (cobalamin deficiency) cblB type This gene encodes a protein that catalyzes the final step in the conversion of vitamin B(12) into adenosylcobalamin (AdoCbl), a vitamin B12-containing coenzyme for methylmalonyl-CoA mutase. Mutations in the gene are the cause of vitamin B12-dependent methylmalonic aciduria linked to the cblB complementation group. Alternatively spliced transcript variants have been found. [provided by RefSeq, Apr 2011] |
SHFLD3 GeneSplit-hand/foot malformation with long bone deficiency 3 |
CILD4 GeneCiliary dyskinesia, primary, 4 |
GCCD2 GeneGlucocorticoid deficiency 2 |
GCCD3 Geneglucocorticoid deficiency 3 |
IGAD1 Geneimmunoglobulin A (IgA) deficiency susceptibility 1 |
PSC GeneCholangitis, primary sclerosing |
PIFO Geneprimary cilia formation Enables cytoskeletal protein binding activity and enzyme binding activity. Involved in positive regulation of kinase activity. Predicted to be located in ciliary basal body and trans-Golgi network. [provided by Alliance of Genome Resources, Mar 2025] |
IPOX GeneIntestinal pseudoobstruction, neuronal, primary idiopathic |
MMACHC Genemethylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria The exact function of the protein encoded by this gene is not known, however, its C-terminal region shows similarity to TonB, a bacterial protein involved in energy transduction for cobalamin (vitamin B12) uptake. Hence, it is postulated that this protein may have a role in the binding and intracellular trafficking of cobalamin. Mutations in this gene are associated with methylmalonic aciduria and homocystinuria type cblC. [provided by RefSeq, Oct 2009] |
SHFLD2 GeneSplit-hand/foot malformation with long deficiency 2 |
MMADHC Genemethylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria This gene encodes a mitochondrial protein that is involved in an early step of vitamin B12 metabolism. Vitamin B12 (cobalamin) is essential for normal development and survival in humans. Mutations in this gene cause methylmalonic aciduria and homocystinuria type cblD (MMADHC), a disorder of cobalamin metabolism that is characterized by decreased levels of the coenzymes adenosylcobalamin and methylcobalamin. Pseudogenes have been identified on chromosomes 11 and X.[provided by RefSeq, Nov 2008] |
AGMX2 Geneagammaglobulinemia, X-linked 2 (with growth hormone deficiency) |
PPH2 Geneprimary pulmonary hypertension 2 |
PLSA1 GenePrimary lateral sclerosis, adult, 1 |
RRDX GeneRadial ray deficiency |
MCFD2P1 Genemultiple coagulation factor deficiency 2 pseudogene 1 |
SHFL1 GeneSplit-hand/foot malformation with long bone deficiency 1 |
MYD88 Genemyeloid differentiation primary response 88 This gene encodes a cytosolic adapter protein that plays a central role in the innate and adaptive immune response. This protein functions as an essential signal transducer in the interleukin-1 and Toll-like receptor signaling pathways. These pathways regulate that activation of numerous proinflammatory genes. The encoded protein consists of an N-terminal death domain and a C-terminal Toll-interleukin1 receptor domain. Patients with defects in this gene have an increased susceptibility to pyogenic bacterial infections. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010] |
PRD Geneprimary retinal dysplasia |
GLC3B Geneglaucoma 3, primary infantile, B |
GLC3C Geneglaucoma 3, primary congenital, C |
HDLCQ14 GeneHypoalphalipoproteinemia, primary |
LOC102724175 Genemembrane primary amine oxidase-like |
LOC100216356 Genemethylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria pseudogene |
LOC100216355 Genemethylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria pseudogene |
CILD8 GeneCiliary dyskinesia, primary, 8 |
CANDN1 Genecandidiasis, nail 1 (with ICAM1 deficiency) |
PBC3 GeneBiliary cirrhosis, primary, 3 |
PBC2 GeneBiliary cirrhosis, primary, 2 |
PBC5 GeneBiliary cirrhosis, primary, 5 |
PBC4 GeneBiliary cirrhosis, primary, 4 |
DPCD Genedeleted in primary ciliary dyskinesia homolog (mouse) This gene in mouse encodes a protein that may be involved in the generation and maintenance of ciliated cells. In mouse, expression of this gene increases during ciliated cell differentiation, and disruption of this gene has been linked to primary ciliary dyskinesia. [provided by RefSeq, Jul 2016] |
MCFD2 Genemultiple coagulation factor deficiency 2 This gene encodes a soluble luminal protein with two calmodulin-like EF-hand motifs at its C-terminus. This protein forms a complex with LMAN1 (lectin mannose binding protein 1; also known as ERGIC-53) that facilitates the transport of coagulation factors V (FV) and VIII (FVIII) from the endoplasmic reticulum to the Golgi apparatus via an endoplasmic reticulum Golgi intermediate compartment (ERGIC). Mutations in this gene cause combined deficiency of FV and FVIII (F5F8D); a rare autosomal recessive bleeding disorder characterized by mild to moderate bleeding and coordinate reduction in plasma FV and FVIII levels. This protein has also been shown to maintain stem cell potential in adult central nervous system and is a marker for testicular germ cell tumors. The 3' UTR of this gene contains a transposon-like human repeat element named 'THE 1'. A processed RNA pseudogene of this gene is on chromosome 6p22.1. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Apr 2016] |
NKCD GeneNatural killer cell deficiency, familial isolated |
LOC100130748 Gene3-hydroxyisobutyryl-Coenzyme A hydrolase pseudogene |
COQ5 Genecoenzyme Q5 homolog, methyltransferase (S. cerevisiae) Enables 2-polyprenyl-6-methoxy-1,4-benzoquinone methyltransferase activity. Involved in methylation and ubiquinone biosynthetic process. Located in mitochondrial inner membrane and mitochondrial matrix. Part of ubiquinone biosynthesis complex. Implicated in primary coenzyme Q10 deficiency 9. [provided by Alliance of Genome Resources, Mar 2025] |
COQ4 Genecoenzyme Q4 This gene encodes a component of the coenzyme Q biosynthesis pathway. Coenzyme Q, an essential component of the electron transport chain, shuttles electrons between complexes I or II to complex III of the mitochondrial transport chain. This protein appears to play a structural role in stabilizing a complex that contains most of the coenzyme Q biosynthesis enzymes. Mutations in this gene are associated with mitochondrial disorders linked to coenzyme Q deficiency. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015] |
COQ9 Genecoenzyme Q9 This locus represents a mitochondrial ubiquinone biosynthesis gene. The encoded protein is likely necessary for biosynthesis of coenzyme Q10, as mutations at this locus have been associated with autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency.[provided by RefSeq, Sep 2010] |
COQ7 Genecoenzyme Q7 homolog, ubiquinone (yeast) The protein encoded by this gene is similar to a mitochondrial di-iron containing hydroxylase in Saccharomyces cerevisiae that is involved with ubiquinone biosynthesis. Mutations in the yeast gene lead to slower development and longer life span. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2010] |
COQ6 Genecoenzyme Q6 monooxygenase The protein encoded by this gene belongs to the ubiH/COQ6 family. It is an evolutionarily conserved monooxygenase required for the biosynthesis of coenzyme Q10 (or ubiquinone), which is an essential component of the mitochondrial electron transport chain, and one of the most potent lipophilic antioxidants implicated in the protection of cell damage by reactive oxygen species. Knockdown of this gene in mouse and zebrafish results in decreased growth due to increased apoptosis. Mutations in this gene are associated with autosomal recessive coenzyme Q10 deficiency-6 (COQ10D6), which manifests as nephrotic syndrome with sensorineural deafness. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jun 2012] |
COQ3 Genecoenzyme Q3 methyltransferase Ubiquinone, also known as coenzyme Q, or Q, is a critical component of the electron transport pathways of both eukaryotes and prokaryotes (Jonassen and Clarke, 2000 [PubMed 10777520]). This lipid consists of a hydrophobic isoprenoid tail and a quinone head group. The tail varies in length depending on the organism, but its purpose is to anchor coenzyme Q to the membrane. The quinone head group is responsible for the activity of coenzyme Q in the respiratory chain. The S. cerevisiae COQ3 gene encodes an O-methyltransferase required for 2 steps in the biosynthetic pathway of coenzyme Q. This enzyme methylates an early coenzyme Q intermediate, 3,4-dihydroxy-5-polyprenylbenzoic acid, as well as the final intermediate in the pathway, converting demethyl-ubiquinone to coenzyme Q. The COQ3 gene product is also capable of methylating the distinct prokaryotic early intermediate 2-hydroxy-6-polyprenyl phenol.[supplied by OMIM, Mar 2008] |
COQ2 Genecoenzyme Q2 4-hydroxybenzoate polyprenyltransferase This gene encodes an enzyme that functions in the final steps in the biosynthesis of CoQ (ubiquinone), a redox carrier in the mitochondrial respiratory chain and a lipid-soluble antioxidant. This enzyme, which is part of the coenzyme Q10 pathway, catalyzes the prenylation of parahydroxybenzoate with an all-trans polyprenyl group. Mutations in this gene cause coenzyme Q10 deficiency, a mitochondrial encephalomyopathy, and also COQ2 nephropathy, an inherited form of mitochondriopathy with primary renal involvement. [provided by RefSeq, Oct 2009] |
LOC128136 Gene3-hydroxy-3-methylglutaryl-Coenzyme A synthase 1 (soluble) pseudogene |
LOC101060199 Geneacyl-coenzyme A synthetase ACSM6, mitochondrial-like |
NDUFS5P3 GeneNADH dehydrogenase (ubiquinone) Fe-S protein 5, 15kDa (NADH-coenzyme Q reductase) pseudogene 3 |
NDUFS5P2 GeneNADH dehydrogenase (ubiquinone) Fe-S protein 5, 15kDa (NADH-coenzyme Q reductase) pseudogene 2 |
NDUFS5P7 GeneNADH dehydrogenase (ubiquinone) Fe-S protein 5, 15kDa (NADH-coenzyme Q reductase) pseudogene 7 |
NDUFS5P5 GeneNADH dehydrogenase (ubiquinone) Fe-S protein 5, 15kDa (NADH-coenzyme Q reductase) pseudogene 5 |
NDUFS5P4 GeneNADH dehydrogenase (ubiquinone) Fe-S protein 5, 15kDa (NADH-coenzyme Q reductase) pseudogene 4 |
NDUFS5P1 GeneNADH dehydrogenase (ubiquinone) Fe-S protein 5, 15kDa (NADH-coenzyme Q reductase) pseudogene 1 |
NDUFS1 GeneNADH dehydrogenase (ubiquinone) Fe-S protein 1, 75kDa (NADH-coenzyme Q reductase) The protein encoded by this gene belongs to the complex I 75 kDa subunit family. Mammalian complex I is composed of 45 different subunits. It locates at the mitochondrial inner membrane. This protein has NADH dehydrogenase activity and oxidoreductase activity. It transfers electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. This protein is the largest subunit of complex I and it is a component of the iron-sulfur (IP) fragment of the enzyme. It may form part of the active site crevice where NADH is oxidized. Mutations in this gene are associated with complex I deficiency. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2011] |
NDUFS2 GeneNADH dehydrogenase (ubiquinone) Fe-S protein 2, 49kDa (NADH-coenzyme Q reductase) The protein encoded by this gene is a core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (complex I). Mammalian mitochondrial complex I is composed of at least 43 different subunits, 7 of which are encoded by the mitochondrial genome, and the rest are the products of nuclear genes. The iron-sulfur protein fraction of complex I is made up of 7 subunits, including this gene product. Complex I catalyzes the NADH oxidation with concomitant ubiquinone reduction and proton ejection out of the mitochondria. Mutations in this gene are associated with mitochondrial complex I deficiency. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Oct 2009] |
NDUFS3 GeneNADH dehydrogenase (ubiquinone) Fe-S protein 3, 30kDa (NADH-coenzyme Q reductase) This gene encodes one of the iron-sulfur protein (IP) components of mitochondrial NADH:ubiquinone oxidoreductase (complex I). Mutations in this gene are associated with Leigh syndrome resulting from mitochondrial complex I deficiency.[provided by RefSeq, Apr 2009] |
NDUFS4 GeneNADH dehydrogenase (ubiquinone) Fe-S protein 4, 18kDa (NADH-coenzyme Q reductase) This gene encodes an nuclear-encoded accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (complex I, or NADH:ubiquinone oxidoreductase). Complex I removes electrons from NADH and passes them to the electron acceptor ubiquinone. Mutations in this gene can cause mitochondrial complex I deficiencies such as Leigh syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015] |
NDUFS5 GeneNADH dehydrogenase (ubiquinone) Fe-S protein 5, 15kDa (NADH-coenzyme Q reductase) This gene is a member of the NADH dehydrogenase (ubiquinone) iron-sulfur protein family. The encoded protein is a subunit of the NADH:ubiquinone oxidoreductase (complex I), the first enzyme complex in the electron transport chain located in the inner mitochondrial membrane. Alternative splicing results in multiple transcript variants and pseudogenes have been identified on chromosomes 1, 4 and 17. [provided by RefSeq, May 2010] |
NDUFS6 GeneNADH dehydrogenase (ubiquinone) Fe-S protein 6, 13kDa (NADH-coenzyme Q reductase) This gene encodes a subunit of the NADH:ubiquinone oxidoreductase (complex I), which is the first enzyme complex in the electron transport chain of mitochondria. This complex functions in the transfer of electrons from NADH to the respiratory chain. The subunit encoded by this gene is one of seven subunits in the iron-sulfur protein fraction. Mutations in this gene cause mitochondrial complex I deficiency, a disease that causes a wide variety of clinical disorders, including neonatal disease and adult-onset neurodegenerative disorders.[provided by RefSeq, Oct 2009] |
NDUFS7 GeneNADH dehydrogenase (ubiquinone) Fe-S protein 7, 20kDa (NADH-coenzyme Q reductase) This gene encodes a protein that is a subunit of one of the complexes that forms the mitochondrial respiratory chain. This protein is one of over 40 subunits found in complex I, the nicotinamide adenine dinucleotide (NADH):ubiquinone oxidoreductase. This complex functions in the transfer of electrons from NADH to the respiratory chain, and ubiquinone is believed to be the immediate electron acceptor for the enzyme. Mutations in this gene cause Leigh syndrome due to mitochondrial complex I deficiency, a severe neurological disorder that results in bilaterally symmetrical necrotic lesions in subcortical brain regions. [provided by RefSeq, Jul 2008] |
NDUFS8 GeneNADH dehydrogenase (ubiquinone) Fe-S protein 8, 23kDa (NADH-coenzyme Q reductase) This gene encodes a subunit of mitochondrial NADH:ubiquinone oxidoreductase, or Complex I, a multimeric enzyme of the respiratory chain responsible for NADH oxidation, ubiquinone reduction, and the ejection of protons from mitochondria. The encoded protein is involved in the binding of two of the six to eight iron-sulfur clusters of Complex I and, as such, is required in the electron transfer process. Mutations in this gene have been associated with Leigh syndrome. [provided by RefSeq, Mar 2010] |
COQ8B Genecoenzyme Q8B This gene encodes a protein with two copies of a domain found in protein kinases. The encoded protein has a complete protein kinase catalytic domain, and a truncated domain that contains only the active and binding sites of the protein kinase domain, however, it is not known whether the protein has any kinase activity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011] |
COQ8A Genecoenzyme Q8A This gene encodes a mitochondrial protein similar to yeast ABC1, which functions in an electron-transferring membrane protein complex in the respiratory chain. It is not related to the family of ABC transporter proteins. Expression of this gene is induced by the tumor suppressor p53 and in response to DNA damage, and inhibiting its expression partially suppresses p53-induced apoptosis. Alternatively spliced transcript variants have been found; however, their full-length nature has not been determined. [provided by RefSeq, Jul 2008] |
Coenzyme Q10 deficiency, primary, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Coenzyme Q10 deficiency, primary, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
coenzyme q10 deficiency, primary, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the coenzyme q10 deficiency, primary, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
Coenzyme Q10 deficiency, primary, 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Coenzyme Q10 deficiency, primary, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Coenzyme Q10 deficiency, primary, 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Coenzyme Q10 deficiency, primary, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Coenzyme Q10 deficiency, primary, 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Coenzyme Q10 deficiency, primary, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
COENZYME Q10 DEFICIENCY, PRIMARY, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease COENZYME Q10 DEFICIENCY, PRIMARY, 1 from the curated CTD Gene-Disease Associations dataset. |
coenzyme q10 deficiency, primary, 6 Gene SetFrom OMIM Gene-Disease Associations genes associated with the coenzyme q10 deficiency, primary, 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
coenzyme q10 deficiency, primary, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the coenzyme q10 deficiency, primary, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
coenzyme q10 deficiency, primary, 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the coenzyme q10 deficiency, primary, 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
coenzyme q10 deficiency, primary, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the coenzyme q10 deficiency, primary, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
coenzyme q10 deficiency, primary, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the coenzyme q10 deficiency, primary, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
Primary coenzyme Q10 deficiency 8 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary coenzyme Q10 deficiency 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary coenzyme Q10 deficiency 6 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary coenzyme Q10 deficiency 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary coenzyme Q10 deficiency 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary coenzyme Q10 deficiency 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary coenzyme Q10 deficiency 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary coenzyme Q10 deficiency 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary coenzyme Q10 deficiency 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary coenzyme Q10 deficiency 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary coenzyme Q10 deficiency 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary coenzyme Q10 deficiency 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary coenzyme Q10 deficiency 7 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary coenzyme Q10 deficiency 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary coenzyme Q10 deficiency 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary coenzyme Q10 deficiency 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary coenzyme Q10 deficiency 9 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary coenzyme Q10 deficiency 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Primary coenzyme Q10 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Primary coenzyme Q10 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Coenzyme Q10 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Coenzyme Q10 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
coenzyme q10 deficiency disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease coenzyme q10 deficiency disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
Coenzyme Q10 Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Coenzyme Q10 Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Coenzyme Q10 deficiency disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Coenzyme Q10 deficiency disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Coenzyme Q10 deficiency disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Coenzyme Q10 deficiency disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Coenzyme Q10 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Coenzyme Q10 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
coenzyme Q10 Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical coenzyme Q10 from the curated CTD Gene-Chemical Interactions dataset. |
Coenzyme Q10 Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Coenzyme Q10 metabolite from the curated HMDB Metabolites of Enzymes dataset. |
Coenzyme Q10 levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Coenzyme Q10 levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Medium-chain acyl-coenzyme A dehydrogenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Medium-chain acyl-coenzyme A dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Multiple Acyl Coenzyme A Dehydrogenase Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Multiple Acyl Coenzyme A Dehydrogenase Deficiency from the curated CTD Gene-Disease Associations dataset. |
disorder of muscle, unspec; lipidoses; lipoidosis; multiple acyl coenzyme a dehydrogenase deficiency; muscular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease disorder of muscle, unspec; lipidoses; lipoidosis; multiple acyl coenzyme a dehydrogenase deficiency; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Multiple Acyl Coenzyme A Dehydrogenase Deficiency Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Multiple Acyl Coenzyme A Dehydrogenase Deficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Nicotinamide Adenine Dinucleotide Coenzyme Q Reductase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Nicotinamide Adenine Dinucleotide Coenzyme Q Reductase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Multiple Acyl Coenzyme A Dehydrogenase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Multiple Acyl Coenzyme A Dehydrogenase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Succinate-Coenzyme Q Reductase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Succinate-Coenzyme Q Reductase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Methylmalonyl-Coenzyme A Mutase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Methylmalonyl-Coenzyme A Mutase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Medium-chain acyl-coenzyme A dehydrogenase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Medium-chain acyl-coenzyme A dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
q10 Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term q10 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glaucoma, primary open-angle; glaucoma, primary congenital Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glaucoma, primary open-angle; glaucoma, primary congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
methyl-tetrahydromethanopterin:coenzyme m methyltransferase complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the methyl-tetrahydromethanopterin:coenzyme m methyltransferase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
Acyl Coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Acyl Coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
succinyl-coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical succinyl-coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
lauroyl-coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical lauroyl-coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
linoleoyl-coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical linoleoyl-coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
oleoyl-coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical oleoyl-coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
nafenopin-coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical nafenopin-coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
arachidoyl-coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical arachidoyl-coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
stearoyl-coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical stearoyl-coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
ciprofibrate-coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical ciprofibrate-coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
arachidonyl-coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical arachidonyl-coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
Palmitoyl Coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Palmitoyl Coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
S-tetradecanoyl-coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical S-tetradecanoyl-coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
Malonyl Coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Malonyl Coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
decanoyl-coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical decanoyl-coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
glutaryl-coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical glutaryl-coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
Coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
valproyl-coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical valproyl-coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
hexanoyl-coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical hexanoyl-coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
Acetyl Coenzyme A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Acetyl Coenzyme A from the curated CTD Gene-Chemical Interactions dataset. |
Coenzyme A Gene Setinteracting proteins for the Coenzyme A drug from the curated DrugBank Drug Targets dataset. |
Octanoyl-Coenzyme A Gene Setinteracting proteins for the Octanoyl-Coenzyme A drug from the curated DrugBank Drug Targets dataset. |
Alpha-Fluoro-Carboxymethyldethia Coenzyme a Complex Gene Setinteracting proteins for the Alpha-Fluoro-Carboxymethyldethia Coenzyme a Complex drug from the curated DrugBank Drug Targets dataset. |
Hexanoyl-Coenzyme A Gene Setinteracting proteins for the Hexanoyl-Coenzyme A drug from the curated DrugBank Drug Targets dataset. |
Nitromethyldethia Coenzyme A Gene Setinteracting proteins for the Nitromethyldethia Coenzyme A drug from the curated DrugBank Drug Targets dataset. |
Coenzyme a Persulfide Gene Setinteracting proteins for the Coenzyme a Persulfide drug from the curated DrugBank Drug Targets dataset. |
Methacrylyl-Coenzyme A Gene Setinteracting proteins for the Methacrylyl-Coenzyme A drug from the curated DrugBank Drug Targets dataset. |
3-Thiaoctanoyl-Coenzyme A Gene Setinteracting proteins for the 3-Thiaoctanoyl-Coenzyme A drug from the curated DrugBank Drug Targets dataset. |
3-Hydroxybutyryl-Coenzyme A Gene Setinteracting proteins for the 3-Hydroxybutyryl-Coenzyme A drug from the curated DrugBank Drug Targets dataset. |
Sinapoyl Coenzyme A Gene Setinteracting proteins for the Sinapoyl Coenzyme A drug from the curated DrugBank Drug Targets dataset. |
Trifluoroacetonyl Coenzyme A Gene Setinteracting proteins for the Trifluoroacetonyl Coenzyme A drug from the curated DrugBank Drug Targets dataset. |
Feruloyl Coenzyme A Gene Setinteracting proteins for the Feruloyl Coenzyme A drug from the curated DrugBank Drug Targets dataset. |
Acetoacetyl-Coenzyme A Gene Setinteracting proteins for the Acetoacetyl-Coenzyme A drug from the curated DrugBank Drug Targets dataset. |
coenzyme Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term coenzyme in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
oxidoreduction coenzyme metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the oxidoreduction coenzyme metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
coenzyme a catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the coenzyme a catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of coenzyme metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of coenzyme metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
coenzyme metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the coenzyme metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
coenzyme a metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the coenzyme a metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
coenzyme a transmembrane transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the coenzyme a transmembrane transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
coenzyme biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the coenzyme biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
coenzyme a transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the coenzyme a transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
coenzyme catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the coenzyme catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
coenzyme a biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the coenzyme a biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
coenzyme transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the coenzyme transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
coenzyme transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the coenzyme transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
coenzyme a transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the coenzyme a transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
coenzyme binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the coenzyme binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Coenzyme Q9 Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Coenzyme Q9 metabolite from the curated HMDB Metabolites of Enzymes dataset. |
Cervonyl coenzyme A Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Cervonyl coenzyme A metabolite from the curated HMDB Metabolites of Enzymes dataset. |
Coenzyme A Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Coenzyme A metabolite from the curated HMDB Metabolites of Enzymes dataset. |
Tetracosapentaenoyl coenzyme A, n-6 Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Tetracosapentaenoyl coenzyme A, n-6 metabolite from the curated HMDB Metabolites of Enzymes dataset. |
Dihomo-gamma-linolenyl coenzyme A Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Dihomo-gamma-linolenyl coenzyme A metabolite from the curated HMDB Metabolites of Enzymes dataset. |
abnormal enzyme/coenzyme activity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal enzyme/coenzyme activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
coenzyme A biosynthesis Gene SetFrom HumanCyc Pathways proteins participating in the coenzyme A biosynthesis pathway from the HumanCyc Pathways dataset. |
Acetyl-coenzyme A transporter 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Acetyl-coenzyme A transporter 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
AmpG-like permease/Acetyl-coenzyme A transporter 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the AmpG-like permease/Acetyl-coenzyme A transporter 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Hydroxymethylglutaryl-coenzyme A synthase, N-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Hydroxymethylglutaryl-coenzyme A synthase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Hydroxymethylglutaryl-coenzyme A synthase C-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Hydroxymethylglutaryl-coenzyme A synthase C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Acetyl-coenzyme A carboxyltransferase, N-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Acetyl-coenzyme A carboxyltransferase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Coenzyme A transferase binding site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Coenzyme A transferase binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Hydroxymethylglutaryl-coenzyme A synthase, active site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Hydroxymethylglutaryl-coenzyme A synthase, active site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Coenzyme A transferase active site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Coenzyme A transferase active site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Acyl-coenzyme A oxidase, N-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Acyl-coenzyme A oxidase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Acetyl-coenzyme A carboxyltransferase, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Acetyl-coenzyme A carboxyltransferase, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
2-amino-3-ketobutyrate coenzyme A ligase Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the 2-amino-3-ketobutyrate coenzyme A ligase protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Coenzyme A transferase family I Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Coenzyme A transferase family I protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
abnormal enzyme/ coenzyme level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal enzyme/ coenzyme level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal enzyme/coenzyme activity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal enzyme/coenzyme activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Coenzyme A linked carnitine metabolism Gene SetFrom PANTHER Pathways proteins participating in the Coenzyme A linked carnitine metabolism pathway from the PANTHER Pathways dataset. |
Coenzyme A biosynthesis Gene SetFrom PANTHER Pathways proteins participating in the Coenzyme A biosynthesis pathway from the PANTHER Pathways dataset. |
Coenzyme A biosynthesis Gene Setproteins participating in the Coenzyme A biosynthesis pathway from the Reactome Pathways dataset. |
Coenzyme A Synthase Protein Associated Neurodegeneration Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Coenzyme A Synthase Protein Associated Neurodegeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormal Enzyme/Coenzyme Activity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Enzyme/Coenzyme Activity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
coenzyme A catabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the coenzyme A catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
coenzyme A biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the coenzyme A biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
coenzyme A metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the coenzyme A metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
coenzyme A transmembrane transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the coenzyme A transmembrane transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
mitochondrial coenzyme A transmembrane transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the mitochondrial coenzyme A transmembrane transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
coenzyme A transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the coenzyme A transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
coenzyme A transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the coenzyme A transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
coenzyme A binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the coenzyme A binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
acyl-coenzyme A diphosphatase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the acyl-coenzyme A diphosphatase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
abnormal enzyme/coenzyme level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal enzyme/coenzyme level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal enzyme/coenzyme activity Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal enzyme/coenzyme activity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Coenzyme A Gene SetFrom MW Enzyme Metabolite Associations interacting proteins for Coenzyme A metabolite from the MW Gene Metabolite Associations dataset. |
Cobamide coenzyme Gene SetFrom MW Enzyme Metabolite Associations interacting proteins for Cobamide coenzyme metabolite from the MW Gene Metabolite Associations dataset. |
Coenzyme A biosynthesis Gene Setproteins participating in the Coenzyme A biosynthesis pathway from the Reactome Pathways 2024 dataset. |
coenzyme A catabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the coenzyme A catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
coenzyme A biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the coenzyme A biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
coenzyme A metabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the coenzyme A metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
coenzyme A transmembrane transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the coenzyme A transmembrane transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
mitochondrial coenzyme A transmembrane transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the mitochondrial coenzyme A transmembrane transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
coenzyme A transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the coenzyme A transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
coenzyme A diphosphatase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the coenzyme A diphosphatase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
coenzyme A transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the coenzyme A transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Methyl coenzyme M reductase complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Methyl coenzyme M reductase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
methyl-tetrahydromethanopterin:coenzyme M methyltransferase complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the methyl-tetrahydromethanopterin:coenzyme M methyltransferase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
systemic primary carnitine deficiency disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease systemic primary carnitine deficiency disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
systemic primary carnitine deficiency disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease systemic primary carnitine deficiency disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
carnitine deficiency, systemic primary Gene SetFrom OMIM Gene-Disease Associations genes associated with the carnitine deficiency, systemic primary phenotype from the curated OMIM Gene-Disease Associations dataset. |
Primary Cd59 Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Cd59 Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Immunodeficiency Syndrome Due To P14 Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Immunodeficiency Syndrome Due To P14 Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Primary Lactase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Primary Lactase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Defective SLC22A5 causes systemic primary carnitine deficiency (CDSP) Gene Setproteins participating in the Defective SLC22A5 causes systemic primary carnitine deficiency (CDSP) pathway from the Reactome Pathways 2024 dataset. |
Systemic primary carnitine deficiency disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Systemic primary carnitine deficiency disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Systemic primary carnitine deficiency disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Systemic primary carnitine deficiency disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Short stature due to primary acid-labile subunit deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Short stature due to primary acid-labile subunit deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Primary immunodeficiency syndrome due to p14 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Primary immunodeficiency syndrome due to p14 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Primary CD59 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Primary CD59 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Neuraminidase deficiency with beta-galactosidase deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuraminidase deficiency with beta-galactosidase deficiency from the curated CTD Gene-Disease Associations dataset. |
MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE from the curated CTD Gene-Disease Associations dataset. |
eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia, iron-deficiency; iron deficiency anaemia; tuberculosis, pulmonary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
folic acid deficiency; fractures, bone; osteoporosis, postmenopausal; riboflavin deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease folic acid deficiency; fractures, bone; osteoporosis, postmenopausal; riboflavin deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia; iron overload Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
choline deficiency; dna damage; folic acid deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease choline deficiency; dna damage; folic acid deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
folic acid deficiency; pregnancy complications; prenatal exposure delayed effects; psychomotor disorders; vitamin b 12 deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease folic acid deficiency; pregnancy complications; prenatal exposure delayed effects; psychomotor disorders; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia, iron-deficiency; beta thalassemia; beta-thalassemia; iron deficiency anaemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; beta thalassemia; beta-thalassemia; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia, iron-deficiency; iron deficiency anaemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
protein c deficiency; protein s deficiency; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease protein c deficiency; protein s deficiency; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
folic acid deficiency; hyperhomocysteinemia; thromboembolism; venous insufficiency; vitamin b 12 deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease folic acid deficiency; hyperhomocysteinemia; thromboembolism; venous insufficiency; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia, iron-deficiency; iron deficiency anaemia; iron overload Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; iron deficiency anaemia; iron overload in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
neoplasms; protein c deficiency; protein s deficiency; venous thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease neoplasms; protein c deficiency; protein s deficiency; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease anemia, iron-deficiency; hemochromatosis; iron deficiency anaemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; folic acid deficiency; hyperhomocysteinemia; kidney failure, chronic; vitamin b 12 deficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; folic acid deficiency; hyperhomocysteinemia; kidney failure, chronic; vitamin b 12 deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Defective GSS causes Glutathione synthetase deficiency (GSS deficiency) Gene Setproteins participating in the Defective GSS causes Glutathione synthetase deficiency (GSS deficiency) pathway from the Reactome Pathways dataset. |
Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency) Gene Setproteins participating in the Defective CYP11B2 causes Corticosterone methyloxidase 1 deficiency (CMO-1 deficiency) pathway from the Reactome Pathways dataset. |
Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency) Gene Setproteins participating in the Defective TPMT causes Thiopurine S-methyltransferase deficiency (TPMT deficiency) pathway from the Reactome Pathways dataset. |
Defective HK1 causes hexokinase deficiency (HK deficiency) Gene Setproteins participating in the Defective HK1 causes hexokinase deficiency (HK deficiency) pathway from the Reactome Pathways 2024 dataset. |
Sulfite oxidase deficiency due to molybdenum cofactor deficiency Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Sulfite oxidase deficiency due to molybdenum cofactor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Primary somatosensory area, trunk Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, trunk relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, trunk, layer 6b Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, trunk, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, trunk, layer 6a Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, trunk, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, mouth, layer 1 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, mouth, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, mouth, layer 5 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, mouth, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, mouth, layer 4 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, mouth, layer 4 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary motor area, Layer 1 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary motor area, Layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary motor area, Layer 5 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary motor area, Layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, upper limb, layer 2/3 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, upper limb, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary visual area, layer 2/3 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary visual area, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, unassigned Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, unassigned relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary motor area Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary motor area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary visual area, layer 6b Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary visual area, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary visual area, layer 6a Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary visual area, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, barrel field, layer 2/3 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, barrel field, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, upper limb Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, upper limb relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary motor area, Layer 2/3 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary motor area, Layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, unassigned, layer 1 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, unassigned, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, unassigned, layer 5 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, unassigned, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, unassigned, layer 4 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, unassigned, layer 4 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, lower limb, layer 2/3 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, lower limb, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary motor area, Layer 6b Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary motor area, Layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary motor area, Layer 6a Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary motor area, Layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, lower limb Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, lower limb relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, nose, layer 6b Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, nose, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, nose, layer 6a Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, nose, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, nose Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, nose relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, mouth Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, mouth relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, unassigned, layer 2/3 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, unassigned, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, lower limb, layer 4 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, lower limb, layer 4 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, lower limb, layer 5 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, lower limb, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, lower limb, layer 1 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, lower limb, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, barrel field Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, barrel field relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, lower limb, layer 6a Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, lower limb, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, lower limb, layer 6b Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, lower limb, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, upper limb, layer 1 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, upper limb, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, upper limb, layer 5 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, upper limb, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, upper limb, layer 4 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, upper limb, layer 4 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, mouth, layer 2/3 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, mouth, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, mouth, layer 6a Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, mouth, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, mouth, layer 6b Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, mouth, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary visual area, layer 1 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary visual area, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary visual area, layer 4 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary visual area, layer 4 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary visual area, layer 5 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary visual area, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, unassigned, layer 6a Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, unassigned, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, unassigned, layer 6b Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, unassigned, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, barrel field, layer 6b Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, barrel field, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, barrel field, layer 6a Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, barrel field, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary visual area Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary visual area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, trunk, layer 2/3 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, trunk, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, upper limb, layer 6a Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, upper limb, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, upper limb, layer 6b Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, upper limb, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, trunk, layer 1 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, trunk, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, trunk, layer 4 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, trunk, layer 4 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, trunk, layer 5 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, trunk, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, barrel field, layer 1 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, barrel field, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, barrel field, layer 5 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, barrel field, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, barrel field, layer 4 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, barrel field, layer 4 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
primary auditory cortex (core)_36 yrs_M_12302 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_13 pcw_F_12834 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_4 yrs_M_12298 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_4 yrs_M_12298 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_23 yrs_M_12300 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary auditory cortex (core)_12 pcw_F_12835 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor cortex (area M1, area 4)_3 yrs_F_12836 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary auditory cortex (core)_24 pcw_M_12288 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_10 mos_M_12977 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_10 mos_M_12977 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary auditory cortex (core)_23 yrs_M_12300 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor cortex (area M1, area 4)_30 yrs_F_12290 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_21 pcw_F_12365 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_21 pcw_F_12365 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_12 pcw_F_12835 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor cortex (area M1, area 4)_18 yrs_M_12984 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_4 mos_M_12296 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_40 yrs_F_12304 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_16 pcw_M_12837 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_13 pcw_F_12834 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary auditory cortex (core)_4 yrs_M_12298 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_4 yrs_M_12298 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary auditory cortex (core)_3 yrs_F_12836 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_12 pcw_F_13060 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor cortex (area M1, area 4)_23 yrs_M_12300 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_36 yrs_M_12302 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor-sensory cortex (samples)_16 pcw_M_12879 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor-sensory cortex (samples)_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor cortex (area M1, area 4)_12 pcw_F_13060 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor-sensory cortex (samples)_8 pcw_M_13058 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor-sensory cortex (samples)_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor cortex (area M1, area 4)_13 pcw_M_12820 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_13 pcw_M_12820 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary auditory cortex (core)_21 yrs_F_13057 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor cortex (area M1, area 4)_8 yrs_M_12841 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_37 yrs_M_12303 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor cortex (area M1, area 4)_12 pcw_F_12835 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor cortex (area M1, area 4)_21 yrs_F_13057 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary auditory cortex (core)_18 yrs_M_12984 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_3 yrs_F_12836 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary auditory cortex (core)_13 pcw_M_12888 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_4 mos_M_12296 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor cortex (area M1, area 4)_4 mos_M_12296 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor cortex (area M1, area 4)_2 yrs_F_12979 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_8 yrs_M_12841 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor cortex (area M1, area 4)_24 pcw_M_12288 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_3 yrs_M_12980 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_13 pcw_M_12888 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_15 yrs_M_12299 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_15 yrs_M_12299 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_4 yrs_M_12298 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_4 yrs_M_12298 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_1 yrs_F_12830 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_3 yrs_F_12836 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary auditory cortex (core)_15 yrs_M_12299 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_15 yrs_M_12299 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_13 yrs_F_12831 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12835 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor cortex (area M1, area 4)_13 pcw_F_12834 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary auditory cortex (core)_21 pcw_F_12365 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_21 pcw_F_12365 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary auditory cortex (core)_13 pcw_F_12834 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary auditory cortex (core)_21 pcw_M_12886 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor cortex (area M1, area 4)_15 yrs_M_12299 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_15 yrs_M_12299 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary auditory cortex (core)_30 yrs_F_12290 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor cortex (area M1, area 4)_4 yrs_M_12298 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_4 yrs_M_12298 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12879 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor-sensory cortex (samples)_19 pcw_F_12885 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor-sensory cortex (samples)_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_12 pcw_F_13060 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary auditory cortex (core)_37 yrs_M_12303 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_3 yrs_M_12980 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_15 yrs_M_12299 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_15 yrs_M_12299 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor cortex (area M1, area 4)_3 yrs_M_12980 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_12 pcw_F_12960 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_12 pcw_F_12960 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary auditory cortex (core)_40 yrs_F_12304 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary auditory cortex (core)_12 pcw_F_13060 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor cortex (area M1, area 4)_16 pcw_M_12837 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary auditory cortex (core)_3 yrs_M_12980 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary auditory cortex (core)_25 pcw_F_12948 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_25 pcw_F_12948 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12837 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_17 pcw_F_12880 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor cortex (area M1, area 4)_1 yrs_F_12830 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_21 yrs_F_13057 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary auditory cortex (core)_16 pcw_M_12879 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary auditory cortex (core)_16 pcw_M_12287 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_16 pcw_M_12287 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_19 pcw_F_12885 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary auditory cortex (core)_12 pcw_F_12960 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_12 pcw_F_12960 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_13 pcw_M_12888 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_26 pcw_F_12949 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_26 pcw_F_12949 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary auditory cortex (core)_13 yrs_F_12831 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_8 yrs_M_12841 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor cortex (area M1, area 4)_12 pcw_F_12960 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_12 pcw_F_12960 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor cortex (area M1, area 4)_36 yrs_M_12302 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_40 yrs_F_12304 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_24 pcw_M_12288 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor cortex (area M1, area 4)_21 pcw_M_12886 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_18 yrs_M_12984 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor cortex (area M1, area 4)_37 yrs_M_12303 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary auditory cortex (core)_19 pcw_F_12885 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_24 pcw_M_12288 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_13 yrs_F_12831 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary auditory cortex (core)_4 mos_M_12296 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor cortex (area M1, area 4)_21 pcw_F_12365 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_21 pcw_F_12365 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_13 pcw_M_12820 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_13 pcw_M_12820 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_21 pcw_F_12365 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_21 pcw_F_12365 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_21 pcw_M_12886 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor-sensory cortex (samples)_16 pcw_M_12287 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor-sensory cortex (samples)_16 pcw_M_12287 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor-sensory cortex (samples)_17 pcw_F_12880 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor-sensory cortex (samples)_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12960 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12960 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_2 yrs_F_12979 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor cortex (area M1, area 4)_40 yrs_F_12304 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_1 yrs_F_12830 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_10 mos_M_12977 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_10 mos_M_12977 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_36 yrs_M_12302 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_2 yrs_F_12979 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_30 yrs_F_12290 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary auditory cortex (core)_1 yrs_F_12830 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_30 yrs_F_12290 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary auditory cortex (core)_13 pcw_M_12820 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_13 pcw_M_12820 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_21 yrs_F_13057 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary auditory cortex (core)_17 pcw_F_12880 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_21 pcw_M_12886 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor cortex (area M1, area 4)_13 pcw_M_12888 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_37 yrs_M_12303 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary auditory cortex (core)_8 yrs_M_12841 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary auditory cortex (core)_2 yrs_F_12979 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary auditory cortex (core)_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_18 yrs_M_12984 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_23 yrs_M_12300 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor cortex (area M1, area 4)_13 yrs_F_12831 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor cortex (area M1, area 4)_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12287 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12287 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary motor-sensory cortex (samples)_9 pcw_M_12833 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in primary motor-sensory cortex (samples)_9 pcw_M_12833 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
primary auditory cortex (core)_36 yrs_M_12302 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_13 pcw_F_12834 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor cortex (area M1, area 4)_21 pcw_M_12886 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary auditory cortex (core)_12 pcw_F_12835 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary auditory cortex (core)_24 pcw_M_12288 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_10 mos_M_12977 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_10 mos_M_12977 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary auditory cortex (core)_23 yrs_M_12300 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_4 mos_M_12890 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_4 mos_M_12890 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor cortex (area M1, area 4)_30 yrs_F_12290 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_12 pcw_F_12835 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor cortex (area M1, area 4)_18 yrs_M_12984 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_4 mos_M_12296 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_40 yrs_F_12304 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_16 pcw_M_12837 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_13 pcw_F_12834 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_3 yrs_F_12836 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary auditory cortex (core)_3 yrs_F_12836 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_12 pcw_F_13060 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor cortex (area M1, area 4)_23 yrs_M_12300 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_36 yrs_M_12302 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor-sensory cortex (samples)_16 pcw_M_12879 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor-sensory cortex (samples)_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor cortex (area M1, area 4)_12 pcw_F_13060 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary auditory cortex (core)_21 yrs_F_13057 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor cortex (area M1, area 4)_8 yrs_M_12841 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_37 yrs_M_12303 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor cortex (area M1, area 4)_12 pcw_F_12835 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_13 yrs_F_12831 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_4 mos_M_12890 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_4 mos_M_12890 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor cortex (area M1, area 4)_21 yrs_F_13057 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary auditory cortex (core)_13 pcw_M_12888 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_8 yrs_M_12841 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_3 yrs_M_12980 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_13 pcw_M_12888 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_1 yrs_F_12830 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_13 yrs_F_12831 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12835 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor cortex (area M1, area 4)_13 pcw_F_12834 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor cortex (area M1, area 4)_4 mos_M_12890 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_4 mos_M_12890 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary auditory cortex (core)_13 pcw_F_12834 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor cortex (area M1, area 4)_37 pcw_M_263195015 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_37 pcw_M_263195015 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor cortex (area M1, area 4)_24 pcw_M_12288 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12879 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor-sensory cortex (samples)_19 pcw_F_12885 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor-sensory cortex (samples)_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_12 pcw_F_13060 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary auditory cortex (core)_37 yrs_M_12303 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary auditory cortex (core)_30 yrs_F_12290 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_3 yrs_M_12980 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary auditory cortex (core)_11 yrs_F_12289 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_11 yrs_F_12289 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor cortex (area M1, area 4)_3 yrs_M_12980 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_12 pcw_F_12960 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_12 pcw_F_12960 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary auditory cortex (core)_12 pcw_F_13060 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor cortex (area M1, area 4)_16 pcw_M_12837 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_17 pcw_F_12880 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_24 pcw_M_12288 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_8 yrs_M_12981 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_8 yrs_M_12981 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor cortex (area M1, area 4)_11 yrs_F_12289 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_11 yrs_F_12289 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary auditory cortex (core)_3 yrs_M_12980 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary auditory cortex (core)_40 yrs_F_12304 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12837 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor cortex (area M1, area 4)_1 yrs_F_12830 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_21 yrs_F_13057 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary auditory cortex (core)_16 pcw_M_12879 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary auditory cortex (core)_16 pcw_M_12287 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_16 pcw_M_12287 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary auditory cortex (core)_25 pcw_F_12948 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_25 pcw_F_12948 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary auditory cortex (core)_12 pcw_F_12960 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_12 pcw_F_12960 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_13 pcw_M_12888 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor cortex (area M1, area 4)_3 yrs_F_12836 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_26 pcw_F_12949 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_26 pcw_F_12949 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary auditory cortex (core)_37 pcw_M_263195015 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_37 pcw_M_263195015 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary auditory cortex (core)_13 yrs_F_12831 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_8 yrs_M_12841 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_30 yrs_F_12290 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_19 yrs_F_12832 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_19 yrs_F_12832 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_13 pcw_M_12820 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_13 pcw_M_12820 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_11 yrs_F_12289 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_11 yrs_F_12289 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_37 pcw_M_263195015 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_37 pcw_M_263195015 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor cortex (area M1, area 4)_12 pcw_F_12960 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_12 pcw_F_12960 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor cortex (area M1, area 4)_36 yrs_M_12302 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_40 yrs_F_12304 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor cortex (area M1, area 4)_4 mos_M_12889 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_4 mos_M_12889 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary auditory cortex (core)_16 pcw_M_12837 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_37 pcw_M_263195015 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_37 pcw_M_263195015 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_18 yrs_M_12984 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor cortex (area M1, area 4)_37 yrs_M_12303 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary auditory cortex (core)_19 pcw_F_12885 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_24 pcw_M_12288 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12287 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_16 pcw_M_12287 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary auditory cortex (core)_4 mos_M_12889 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_4 mos_M_12889 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor cortex (area M1, area 4)_19 yrs_F_12832 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_19 yrs_F_12832 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_13 pcw_M_12820 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_13 pcw_M_12820 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_21 pcw_M_12886 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor-sensory cortex (samples)_8 pcw_M_13058 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor-sensory cortex (samples)_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor cortex (area M1, area 4)_13 pcw_M_12820 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_13 pcw_M_12820 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12960 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_12 pcw_F_12960 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor cortex (area M1, area 4)_13 pcw_M_12888 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_2 yrs_F_12979 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor cortex (area M1, area 4)_40 yrs_F_12304 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_19 yrs_F_12832 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_19 yrs_F_12832 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_1 yrs_F_12830 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor-sensory cortex (samples)_17 pcw_F_12880 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor-sensory cortex (samples)_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_10 mos_M_12977 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_10 mos_M_12977 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_36 yrs_M_12302 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_2 yrs_F_12979 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary auditory cortex (core)_18 yrs_M_12984 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_30 yrs_F_12290 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary auditory cortex (core)_1 yrs_F_12830 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary auditory cortex (core)_8 yrs_M_12981 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_8 yrs_M_12981 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_19 pcw_F_12885 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary auditory cortex (core)_13 pcw_M_12820 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_13 pcw_M_12820 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_21 yrs_F_13057 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary auditory cortex (core)_17 pcw_F_12880 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary auditory cortex (core)_4 mos_M_12890 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_4 mos_M_12890 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_21 pcw_M_12886 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary visual cortex (striate cortex, area V1/17)_37 yrs_M_12303 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary visual cortex (striate cortex, area V1/17)_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary auditory cortex (core)_8 yrs_M_12841 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_18 yrs_M_12984 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_23 yrs_M_12300 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor cortex (area M1, area 4)_13 yrs_F_12831 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor cortex (area M1, area 4)_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary somatosensory cortex (area S1, areas 3,1,2)_11 yrs_F_12289 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary somatosensory cortex (area S1, areas 3,1,2)_11 yrs_F_12289 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary auditory cortex (core)_19 yrs_F_12832 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary auditory cortex (core)_19 yrs_F_12832 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
primary motor-sensory cortex (samples)_9 pcw_M_12833 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in primary motor-sensory cortex (samples)_9 pcw_M_12833 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
SP in primary somatosensory cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SP in primary somatosensory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
IZ in primary visual cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in IZ in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
MZ in primary auditory cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in MZ in primary auditory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
IZ in primary somatosensory cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in IZ in primary somatosensory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
outer CP in primary visual cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer CP in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
SG in primary auditory cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SG in primary auditory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
SP in primary visual cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SP in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
outer CP in primary somatosensory cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer CP in primary somatosensory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
SG in primary somatosensory cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SG in primary somatosensory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in primary visual cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
SG in primary visual cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SG in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
outer CP in primary auditory cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer CP in primary auditory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in primary auditory cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in primary auditory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
outer SZ in primary somatosensory cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer SZ in primary somatosensory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner CP in primary somatosensory cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner CP in primary somatosensory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
VZ in primary somatosensory cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in VZ in primary somatosensory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
MZ in primary somatosensory cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in MZ in primary somatosensory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner SZ in primary somatosensory cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in primary somatosensory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
SP in primary auditory cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in SP in primary auditory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
outer SZ in primary visual cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in outer SZ in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
IZ in primary auditory cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in IZ in primary auditory cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
VZ in primary visual cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in VZ in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
MZ in primary visual cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in MZ in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
inner SZ in primary visual cortex Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in inner SZ in primary visual cortex relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
TAL1-20566737-PRIMARY FETAL LIVER ERYTHROID CELLS-MOUSE Gene SetFrom ChEA Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the TAL1-20566737-PRIMARY FETAL LIVER ERYTHROID CELLS-MOUSE transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset. |
Pulmonary hypertension, primary, 1, with hereditary hemorrhagic telangiectasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pulmonary hypertension, primary, 1, with hereditary hemorrhagic telangiectasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary autosomal recessive microcephaly 8 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary autosomal recessive microcephaly 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary autosomal recessive microcephaly 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary autosomal recessive microcephaly 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary autosomal recessive microcephaly 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary autosomal recessive microcephaly 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary autosomal recessive microcephaly 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary autosomal recessive microcephaly 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary autosomal recessive microcephaly 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary autosomal recessive microcephaly 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly 12, primary, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly 12, primary, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary erythromelalgia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary erythromelalgia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary hypertrophic osteoarthropathy, autosomal recessive 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary hypertrophic osteoarthropathy, autosomal recessive 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glaucoma, primary open angle, juvenile-onset Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glaucoma, primary open angle, juvenile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Failure of tooth eruption, primary Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Failure of tooth eruption, primary phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Aphakia, congenital primary Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Aphakia, congenital primary phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lymphedema, primary, with myelodysplasia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lymphedema, primary, with myelodysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary autosomal recessive microcephaly 7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary autosomal recessive microcephaly 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary autosomal recessive microcephaly 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary autosomal recessive microcephaly 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pigmented nodular adrenocortical disease, primary, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pigmented nodular adrenocortical disease, primary, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pigmented nodular adrenocortical disease, primary, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pigmented nodular adrenocortical disease, primary, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pigmented nodular adrenocortical disease, primary, 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pigmented nodular adrenocortical disease, primary, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary hyperoxaluria, type II Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary hyperoxaluria, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary dilated cardiomyopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary dilated cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ciliary dyskinesia, primary, 9 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ciliary dyskinesia, primary, 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ciliary dyskinesia, primary, 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ciliary dyskinesia, primary, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ciliary dyskinesia, primary, 7 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ciliary dyskinesia, primary, 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ciliary dyskinesia, primary, 6 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ciliary dyskinesia, primary, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ciliary dyskinesia, primary, 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ciliary dyskinesia, primary, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Juvenile primary lateral sclerosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Juvenile primary lateral sclerosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly 10, primary, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly 10, primary, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary open angle glaucoma Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary open angle glaucoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Persistent hyperplastic primary vitreous, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Persistent hyperplastic primary vitreous, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pulmonary hypertension, primary, fenfluramine-associated Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pulmonary hypertension, primary, fenfluramine-associated phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary ciliary dyskinesia 24 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary ciliary dyskinesia 24 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary ciliary dyskinesia 23 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary ciliary dyskinesia 23 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Bile acid malabsorption, primary Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Bile acid malabsorption, primary phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary hyperoxaluria, type I Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary hyperoxaluria, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary pulmonary hypertension 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary pulmonary hypertension 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary pulmonary hypertension 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary pulmonary hypertension 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary pulmonary hypertension 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary pulmonary hypertension 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary hyperparathyroidism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary hyperparathyroidism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ciliary dyskinesia, primary, 13 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ciliary dyskinesia, primary, 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ciliary dyskinesia, primary, 12 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ciliary dyskinesia, primary, 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ciliary dyskinesia, primary, 11 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ciliary dyskinesia, primary, 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ciliary dyskinesia, primary, 10 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ciliary dyskinesia, primary, 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ciliary dyskinesia, primary, 17 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ciliary dyskinesia, primary, 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ciliary dyskinesia, primary, 16 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ciliary dyskinesia, primary, 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ciliary dyskinesia, primary, 15 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ciliary dyskinesia, primary, 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ciliary dyskinesia, primary, 14 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ciliary dyskinesia, primary, 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ciliary dyskinesia, primary, 19 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ciliary dyskinesia, primary, 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ciliary dyskinesia, primary, 18 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ciliary dyskinesia, primary, 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary hypomagnesemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary hypomagnesemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary pulmonary hypertension Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary pulmonary hypertension phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ciliary dyskinesia, primary, 30 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ciliary dyskinesia, primary, 30 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary familial hypertrophic cardiomyopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary familial hypertrophic cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pneumothorax, primary spontaneous Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pneumothorax, primary spontaneous phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary hyperoxaluria, type III Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary hyperoxaluria, type III phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ciliary dyskinesia, primary, 28 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ciliary dyskinesia, primary, 28 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ciliary dyskinesia, primary, 29 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ciliary dyskinesia, primary, 29 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ciliary dyskinesia, primary, 22 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ciliary dyskinesia, primary, 22 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ciliary dyskinesia, primary, 20 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ciliary dyskinesia, primary, 20 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ciliary dyskinesia, primary, 21 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ciliary dyskinesia, primary, 21 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ciliary dyskinesia, primary, 26 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ciliary dyskinesia, primary, 26 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Primary open angle glaucoma juvenile onset 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Primary open angle glaucoma juvenile onset 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly 11, primary, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly 11, primary, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly 9, primary, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly 9, primary, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Microcephaly 13, primary, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Microcephaly 13, primary, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
primary cilium Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the primary cilium cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
primary lysosome Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the primary lysosome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
motile primary cilium Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the motile primary cilium cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
nonmotile primary cilium Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the nonmotile primary cilium cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
primary endosperm nucleus Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the primary endosperm nucleus cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
primary cilium Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the primary cilium cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
primary cell wall Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the primary cell wall cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
primary lysosome Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the primary lysosome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
motile primary cilium Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the motile primary cilium cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
nonmotile primary cilium Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the nonmotile primary cilium cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
Neoplasms, Second Primary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neoplasms, Second Primary from the curated CTD Gene-Disease Associations dataset. |
Hyperparathyroidism, Neonatal Severe Primary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hyperparathyroidism, Neonatal Severe Primary from the curated CTD Gene-Disease Associations dataset. |
Biliary Cirrhosis, Primary, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Biliary Cirrhosis, Primary, 2 from the curated CTD Gene-Disease Associations dataset. |
HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1 from the curated CTD Gene-Disease Associations dataset. |
Pneumothorax, Primary Spontaneous Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pneumothorax, Primary Spontaneous from the curated CTD Gene-Disease Associations dataset. |
Pigmented Nodular Adrenocortical Disease, Primary, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pigmented Nodular Adrenocortical Disease, Primary, 1 from the curated CTD Gene-Disease Associations dataset. |
Ciliary Dyskinesia, Primary, 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ciliary Dyskinesia, Primary, 6 from the curated CTD Gene-Disease Associations dataset. |
Ciliary Dyskinesia, Primary, 13 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ciliary Dyskinesia, Primary, 13 from the curated CTD Gene-Disease Associations dataset. |
Ciliary Dyskinesia, Primary, 11 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ciliary Dyskinesia, Primary, 11 from the curated CTD Gene-Disease Associations dataset. |
Ciliary Dyskinesia, Primary, 10 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ciliary Dyskinesia, Primary, 10 from the curated CTD Gene-Disease Associations dataset. |
Hypomagnesemia primary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hypomagnesemia primary from the curated CTD Gene-Disease Associations dataset. |
Aphakia, congenital primary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Aphakia, congenital primary from the curated CTD Gene-Disease Associations dataset. |
Primary Myelofibrosis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Primary Myelofibrosis from the curated CTD Gene-Disease Associations dataset. |
Primary Ovarian Insufficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Primary Ovarian Insufficiency from the curated CTD Gene-Disease Associations dataset. |
Glaucoma 3, primary infantile, B Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glaucoma 3, primary infantile, B from the curated CTD Gene-Disease Associations dataset. |
Ciliary Dyskinesia, Primary, 9 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ciliary Dyskinesia, Primary, 9 from the curated CTD Gene-Disease Associations dataset. |
Ciliary Dyskinesia, Primary, 7 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ciliary Dyskinesia, Primary, 7 from the curated CTD Gene-Disease Associations dataset. |
Ciliary Dyskinesia, Primary, 8 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ciliary Dyskinesia, Primary, 8 from the curated CTD Gene-Disease Associations dataset. |
Neoplasms, Unknown Primary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neoplasms, Unknown Primary from the curated CTD Gene-Disease Associations dataset. |
Bile Acid Malabsorption, Primary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Bile Acid Malabsorption, Primary from the curated CTD Gene-Disease Associations dataset. |
Primary Ovarian Insufficiency, Fragile X-Associated Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Primary Ovarian Insufficiency, Fragile X-Associated from the curated CTD Gene-Disease Associations dataset. |
Primary hyperoxaluria type 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Primary hyperoxaluria type 2 from the curated CTD Gene-Disease Associations dataset. |
GLAUCOMA 3, PRIMARY CONGENITAL, C Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease GLAUCOMA 3, PRIMARY CONGENITAL, C from the curated CTD Gene-Disease Associations dataset. |
Microcephaly, Primary Autosomal Recessive, 5 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Microcephaly, Primary Autosomal Recessive, 5 from the curated CTD Gene-Disease Associations dataset. |
RETINAL DYSPLASIA, PRIMARY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease RETINAL DYSPLASIA, PRIMARY from the curated CTD Gene-Disease Associations dataset. |
Microcephaly, Primary Autosomal Recessive, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Microcephaly, Primary Autosomal Recessive, 4 from the curated CTD Gene-Disease Associations dataset. |
Microcephaly, Primary Autosomal Recessive, 6 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Microcephaly, Primary Autosomal Recessive, 6 from the curated CTD Gene-Disease Associations dataset. |
Failure of Tooth Eruption, Primary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Failure of Tooth Eruption, Primary from the curated CTD Gene-Disease Associations dataset. |
Microcephaly, Primary Autosomal Recessive, 7 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Microcephaly, Primary Autosomal Recessive, 7 from the curated CTD Gene-Disease Associations dataset. |
Primary lateral sclerosis juvenile Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Primary lateral sclerosis juvenile from the curated CTD Gene-Disease Associations dataset. |
Glaucoma, Primary Open Angle Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glaucoma, Primary Open Angle from the curated CTD Gene-Disease Associations dataset. |
Pigmented Nodular Adrenocortical Disease, Primary, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pigmented Nodular Adrenocortical Disease, Primary, 2 from the curated CTD Gene-Disease Associations dataset. |
Polycythemia, primary familial and congenital Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Polycythemia, primary familial and congenital from the curated CTD Gene-Disease Associations dataset. |
T cell immunodeficiency primary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease T cell immunodeficiency primary from the curated CTD Gene-Disease Associations dataset. |
Microcephaly, Primary Autosomal Recessive, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Microcephaly, Primary Autosomal Recessive, 3 from the curated CTD Gene-Disease Associations dataset. |
GLAUCOMA 1, PRIMARY OPEN ANGLE, C Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease GLAUCOMA 1, PRIMARY OPEN ANGLE, C from the curated CTD Gene-Disease Associations dataset. |
Microcephaly, Primary Autosomal Recessive, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Microcephaly, Primary Autosomal Recessive, 1 from the curated CTD Gene-Disease Associations dataset. |
Primary ciliary dyskinesia, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Primary ciliary dyskinesia, 4 from the curated CTD Gene-Disease Associations dataset. |
Osteoarthropathy, Primary Hypertrophic Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Osteoarthropathy, Primary Hypertrophic from the curated CTD Gene-Disease Associations dataset. |
Primary hyperoxaluria type 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Primary hyperoxaluria type 1 from the curated CTD Gene-Disease Associations dataset. |
Ciliary Dyskinesia, Primary, 12 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ciliary Dyskinesia, Primary, 12 from the curated CTD Gene-Disease Associations dataset. |
Glaucoma 3, Primary Congenital, D Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glaucoma 3, Primary Congenital, D from the curated CTD Gene-Disease Associations dataset. |
Glaucoma 3, Primary Congenital, A Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glaucoma 3, Primary Congenital, A from the curated CTD Gene-Disease Associations dataset. |
Primary Lateral Sclerosis, Adult, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Primary Lateral Sclerosis, Adult, 1 from the curated CTD Gene-Disease Associations dataset. |
Primary ciliary dyskinesia, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Primary ciliary dyskinesia, 3 from the curated CTD Gene-Disease Associations dataset. |
HYPEROXALURIA, PRIMARY, TYPE III Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HYPEROXALURIA, PRIMARY, TYPE III from the curated CTD Gene-Disease Associations dataset. |
Cervical Dystonia, Primary Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cervical Dystonia, Primary from the curated CTD Gene-Disease Associations dataset. |
Biliary Cirrhosis, Primary, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Biliary Cirrhosis, Primary, 3 from the curated CTD Gene-Disease Associations dataset. |
primary polycythemia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease primary polycythemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
primary immunodeficiency disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease primary immunodeficiency disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
primary hyperoxaluria Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease primary hyperoxaluria from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
primary pulmonary hypertension Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease primary pulmonary hypertension from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
primary ciliary dyskinesia Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease primary ciliary dyskinesia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
primary bacterial infectious disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease primary bacterial infectious disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
primary biliary cirrhosis Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease primary biliary cirrhosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
primary immunodeficiency disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease primary immunodeficiency disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
primary hyperparathyroidism Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary hyperparathyroidism in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
primary angle-closure glaucoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary angle-closure glaucoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
primary hypertrophic osteoarthropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary hypertrophic osteoarthropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
primary polycythemia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary polycythemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
primary immunodeficiency disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary immunodeficiency disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
primary ciliary dyskinesia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary ciliary dyskinesia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
primary amebic meningoencephalitis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary amebic meningoencephalitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
primary optic atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary optic atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
primary thrombocytopenia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary thrombocytopenia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
primary biliary cirrhosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary biliary cirrhosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
primary cutaneous amyloidosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary cutaneous amyloidosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
primary open angle glaucoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary open angle glaucoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
primary syphilis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary syphilis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
primary pulmonary hypertension Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary pulmonary hypertension in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
primary bacterial infectious disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary bacterial infectious disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
primary systemic mycosis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary systemic mycosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
primary hyperoxaluria Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary hyperoxaluria in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
primary congenital glaucoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary congenital glaucoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
primary cerebellar degeneration Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary cerebellar degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
primary melanomas. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary melanomas. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
primary biliary cirrhosis] Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary biliary cirrhosis] in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
primary congenital glaucoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary congenital glaucoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
primary myelofibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary myelofibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
melanoma; neoplasms, second primary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease melanoma; neoplasms, second primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
primary blepharospasm Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary blepharospasm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
melanoma; neoplasms, multiple primary; nevus; skin neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease melanoma; neoplasms, multiple primary; nevus; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
menarch; natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious Gene SetFrom GAD Gene-Disease Associations genes associated with the disease menarch; natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis, primary biliary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis, primary biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, basal cell; carcinoma, squamous cell; neoplasms, second primary; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; neoplasms, second primary; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis, biliary primary; liver disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis, biliary primary; liver disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; head and neck neoplasms; neoplasms, second primary; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; head and neck neoplasms; neoplasms, second primary; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
primary biliary cirrhosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary biliary cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, myeloid; neoplasms, second primary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, myeloid; neoplasms, second primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis, biliary primary; cholangitis, sclerosing Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis, biliary primary; cholangitis, sclerosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glaucoma, primary open-angle; glaucoma, normal tension Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glaucoma, primary open-angle; glaucoma, normal tension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aphasia, primary progressive; dementia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aphasia, primary progressive; dementia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia; neoplasms, second primary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia; neoplasms, second primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chromosome aberrations; leukemia, myeloid, acute; primary myelofibrosis; thrombocythemia, essential; trisomy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chromosome aberrations; leukemia, myeloid, acute; primary myelofibrosis; thrombocythemia, essential; trisomy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal neoplasms; neoplasms, second primary; oesophageal neoplasm Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal neoplasms; neoplasms, second primary; oesophageal neoplasm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glaucoma, primary open-angle Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glaucoma, primary open-angle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myeloproliferative disorders; philadelphia chromosome; polycythemia vera; primary myelofibrosis; thrombocythemia, essential; thrombocythemia, hemorrhagic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myeloproliferative disorders; philadelphia chromosome; polycythemia vera; primary myelofibrosis; thrombocythemia, essential; thrombocythemia, hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; nerve degeneration Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; nerve degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
laryngeal neoplasm; laryngeal neoplasms; neoplasms, second primary; neoplasms, squamous cell Gene SetFrom GAD Gene-Disease Associations genes associated with the disease laryngeal neoplasm; laryngeal neoplasms; neoplasms, second primary; neoplasms, squamous cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hodgkin disease; leukemia, myeloid, acute; neoplasms, second primary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hodgkin disease; leukemia, myeloid, acute; neoplasms, second primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; aphasia, primary progressive Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; aphasia, primary progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dystonia, primary torsion Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dystonia, primary torsion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, female; pof - premature ovarian failure; primary ovarian insufficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, female; pof - premature ovarian failure; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; head and neck neoplasms; neoplasm metastasis; neoplasm recurrence, local; neoplasms, second primary; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; head and neck neoplasms; neoplasm metastasis; neoplasm recurrence, local; neoplasms, second primary; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
primary progressive aphasia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary progressive aphasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
head and neck neoplasms; neoplasm recurrence, local; neoplasms, second primary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease head and neck neoplasms; neoplasm recurrence, local; neoplasms, second primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; head and neck neoplasms; neoplasm recurrence, local; neoplasms, second primary; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; head and neck neoplasms; neoplasm recurrence, local; neoplasms, second primary; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cell transformation, neoplastic; leukemia; myelofibrosis; primary myelofibrosis; splenomegaly Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cell transformation, neoplastic; leukemia; myelofibrosis; primary myelofibrosis; splenomegaly in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypercalcemia; hyperparathyroidism, primary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypercalcemia; hyperparathyroidism, primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
neoplasms, multiple primary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease neoplasms, multiple primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperoxaluria, primary, type 1 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperoxaluria, primary, type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adrenal gland neoplasms; adrenal neoplasm; neoplasms, multiple primary; paraganglioma; pheochromocytoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adrenal gland neoplasms; adrenal neoplasm; neoplasms, multiple primary; paraganglioma; pheochromocytoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
primary tooth development Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary tooth development in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myeloproliferative disorders; polycythemia vera; primary myelofibrosis; thrombocythemia, essential Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myeloproliferative disorders; polycythemia vera; primary myelofibrosis; thrombocythemia, essential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; memory disorders; neurodegenerative diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; memory disorders; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
primary iga nephropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary iga nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma; hematologic neoplasms; hemochromatosis; myeloproliferative disorders; neoplasms; neoplasms, multiple primary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma; hematologic neoplasms; hemochromatosis; myeloproliferative disorders; neoplasms; neoplasms, multiple primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
primary bone lymphomas. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary bone lymphomas. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
head and neck neoplasms; neoplasms, multiple primary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease head and neck neoplasms; neoplasms, multiple primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
primary myelofibrosis; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary myelofibrosis; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glaucoma, primary congenital Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glaucoma, primary congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
primary myelofibrosis; recurrence; thrombosis; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary myelofibrosis; recurrence; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis, biliary primary; hepatitis type 1, autoimmune (aih-1) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis, biliary primary; hepatitis type 1, autoimmune (aih-1) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
primary open angle glaucoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary open angle glaucoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leukemia, myeloid, acute; neoplasms, second primary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leukemia, myeloid, acute; neoplasms, second primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycythemia vera; primary myelofibrosis; thrombocythemia, essential Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycythemia vera; primary myelofibrosis; thrombocythemia, essential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
colorectal neoplasms, hereditary nonpolyposis; hereditary nonpolyposis colorectal neoplasms; neoplasms, second primary; rectal neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease colorectal neoplasms, hereditary nonpolyposis; hereditary nonpolyposis colorectal neoplasms; neoplasms, second primary; rectal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
primary billiary cirrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary billiary cirrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dna damage; neoplasms, second primary; precursor b-cell lymphoblastic leukemia-lymphoma; precursor t-cell lymphoblastic leukemia-lymphoma; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dna damage; neoplasms, second primary; precursor b-cell lymphoblastic leukemia-lymphoma; precursor t-cell lymphoblastic leukemia-lymphoma; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; head and neck neoplasms; neoplasms, second primary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; head and neck neoplasms; neoplasms, second primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hodgkin disease; neoplasms, second primary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hodgkin disease; neoplasms, second primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
laryngeal neoplasm; laryngeal neoplasms; neoplasms, multiple primary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease laryngeal neoplasm; laryngeal neoplasms; neoplasms, multiple primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hperoxaluria, primary, type 1 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hperoxaluria, primary, type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease; hyperparathyroidism, primary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease; hyperparathyroidism, primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blast crisis; blast phase; polycythemia vera; primary myelofibrosis; thrombocythemia, essential; thrombocythemia, hemorrhagic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blast crisis; blast phase; polycythemia vera; primary myelofibrosis; thrombocythemia, essential; thrombocythemia, hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
pof - premature ovarian failure; primary ovarian insufficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease pof - premature ovarian failure; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
primary hyperparathyroidism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary hyperparathyroidism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sjogren's syndrome, primary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sjogren's syndrome, primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aphasia, primary progressive; heredodegenerative disorders, nervous system Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aphasia, primary progressive; heredodegenerative disorders, nervous system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blepharophimosis; blepharoptosis; pof - premature ovarian failure; primary ovarian insufficiency; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blepharophimosis; blepharoptosis; pof - premature ovarian failure; primary ovarian insufficiency; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; chromosome breakage; head and neck neoplasms; neoplasms, second primary; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; chromosome breakage; head and neck neoplasms; neoplasms, second primary; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
neoplasms, second primary; precursor cell lymphoblastic leukemia-lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease neoplasms, second primary; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
infertility, female; primary ovarian insufficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease infertility, female; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary atresia; liver diseases; primary graft dysfunction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary atresia; liver diseases; primary graft dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperparathyroidism, primary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperparathyroidism, primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
melanoma; neoplasms, multiple primary; skin neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease melanoma; neoplasms, multiple primary; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperparathyroidism, primary; pancreatitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperparathyroidism, primary; pancreatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
primary myelofibrosis; thrombocythemia, essential; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary myelofibrosis; thrombocythemia, essential; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
congenital primary hypothyroidism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease congenital primary hypothyroidism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
primary myelofibrosis; thrombocythemia, essential; thrombocythemia, hemorrhagic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary myelofibrosis; thrombocythemia, essential; thrombocythemia, hemorrhagic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dystonia, primary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dystonia, primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
melanoma, sporadic primary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease melanoma, sporadic primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, basal cell; neoplasms, second primary; skin basal cell carcinoma; skin neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, basal cell; neoplasms, second primary; skin basal cell carcinoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blast crisis; leukemia, megakaryoblastic, acute; leukemia, myelogenous, chronic, bcr-abl positive; primary myelofibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blast crisis; leukemia, megakaryoblastic, acute; leukemia, myelogenous, chronic, bcr-abl positive; primary myelofibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
leiomyoma; neoplasms, multiple primary; uterine neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease leiomyoma; neoplasms, multiple primary; uterine neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, squamous cell; head and neck neoplasms; neoplasms, multiple primary; respiratory tract neoplasms; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, squamous cell; head and neck neoplasms; neoplasms, multiple primary; respiratory tract neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
osteoporosis; cirrhosis, primary biliary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease osteoporosis; cirrhosis, primary biliary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperoxaluria, primary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperoxaluria, primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dystonia, early onset primary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dystonia, early onset primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast neoplasms; mammary neoplasms; neoplasms, multiple primary; ovarian neoplasm; ovarian neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms; mammary neoplasms; neoplasms, multiple primary; ovarian neoplasm; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
primary myelofibrosis; thrombocythemia, essential Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary myelofibrosis; thrombocythemia, essential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
brain neoplasms; leukemia, myeloid, acute; neoplasms, second primary; precursor cell lymphoblastic leukemia-lymphoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease brain neoplasms; leukemia, myeloid, acute; neoplasms, second primary; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis, biliary primary Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis, biliary primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
primary sclerosing cholangitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary sclerosing cholangitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
graves' disease; hashimoto's thyroiditis; primary idiopathic myxedema Gene SetFrom GAD Gene-Disease Associations genes associated with the disease graves' disease; hashimoto's thyroiditis; primary idiopathic myxedema in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
esophageal neoplasms; neoplasms, second primary; oesophageal neoplasm; stomach neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease esophageal neoplasms; neoplasms, second primary; oesophageal neoplasm; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
breast neoplasms; neoplasms, multiple primary; ovarian neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease breast neoplasms; neoplasms, multiple primary; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis, biliary primary; hepatitis, autoimmune Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis, biliary primary; hepatitis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
polycythemia vera; primary myelofibrosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease polycythemia vera; primary myelofibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
menarch; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious Gene SetFrom GAD Gene-Disease Associations genes associated with the disease menarch; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
kidney neoplasms; neoplasms, second primary; wilms tumor Gene SetFrom GAD Gene-Disease Associations genes associated with the disease kidney neoplasms; neoplasms, second primary; wilms tumor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
primary lung adenocarcinomas Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary lung adenocarcinomas in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cell transformation, neoplastic; leucocytosis; leukemia; leukocytosis; polycythemia vera; primary myelofibrosis; vascular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cell transformation, neoplastic; leucocytosis; leukemia; leukocytosis; polycythemia vera; primary myelofibrosis; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenoma; colonic neoplasms; colonic polyps; neoplasms, multiple primary; precancerous conditions Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenoma; colonic neoplasms; colonic polyps; neoplasms, multiple primary; precancerous conditions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
amenorrhea; pof - premature ovarian failure; primary ovarian insufficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease amenorrhea; pof - premature ovarian failure; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
primary lung cancer. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary lung cancer. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cirrhosis, biliary primary; diabetes, gestational Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cirrhosis, biliary primary; diabetes, gestational in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
46, xx disorders of sex development; pof - premature ovarian failure; primary ovarian insufficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease 46, xx disorders of sex development; pof - premature ovarian failure; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
menopause, premature; primary ovarian insufficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease menopause, premature; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypothyroidism; pof - premature ovarian failure; primary ovarian insufficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypothyroidism; pof - premature ovarian failure; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
premature ovarian failure; primary amenorrhea; secondary amenorrhea Gene SetFrom GAD Gene-Disease Associations genes associated with the disease premature ovarian failure; primary amenorrhea; secondary amenorrhea in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
primary open-angle glaucoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease primary open-angle glaucoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glaucoma; glaucoma, primary open-angle Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glaucoma; glaucoma, primary open-angle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic progressive external ophthalmoplegia; ophthalmoplegia, chronic progressive external; pof - premature ovarian failure; primary ovarian insufficiency Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic progressive external ophthalmoplegia; ophthalmoplegia, chronic progressive external; pof - premature ovarian failure; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
primary Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term primary in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Primary pulmonary hypoplasia_Lung Tissue_GSE1363 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Primary pulmonary hypoplasia_Lung Tissue_GSE1363 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
MECP2_KD_GDS4759_334_mouse_E16 primary cortical neuron cultures Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the MECP2_KD_GDS4759_334_mouse_E16 primary cortical neuron cultures gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
FMR1_KD_GDS4759_333_mouse_E16 primary cortical neuron cultures Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the FMR1_KD_GDS4759_333_mouse_E16 primary cortical neuron cultures gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
MEF2A_KD_GDS4759_340_mouse_E16 primary cortical neuron cultures Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the MEF2A_KD_GDS4759_340_mouse_E16 primary cortical neuron cultures gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
NLGN3_KD_GDS4759_336_mouse_E16 primary cortical neuron cultures Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the NLGN3_KD_GDS4759_336_mouse_E16 primary cortical neuron cultures gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
MEF2D_KD_GDS4759_339_mouse_E16 primary cortical neuron cultures Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the MEF2D_KD_GDS4759_339_mouse_E16 primary cortical neuron cultures gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
SHANK3_KD_GDS4759_338_mouse_E16 primary cortical neuron cultures Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the SHANK3_KD_GDS4759_338_mouse_E16 primary cortical neuron cultures gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
NLGN1_KD_GDS4759_335_mouse_E16 primary cortical neuron cultures Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the NLGN1_KD_GDS4759_335_mouse_E16 primary cortical neuron cultures gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
PTEN_KD_GDS4759_337_mouse_E16 primary cortical neuron cultures Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the PTEN_KD_GDS4759_337_mouse_E16 primary cortical neuron cultures gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
development of primary female sexual characteristics Gene SetFrom GO Biological Process Annotations 2015 genes participating in the development of primary female sexual characteristics biological process from the curated GO Biological Process Annotations 2015 dataset. |
development of primary sexual characteristics Gene SetFrom GO Biological Process Annotations 2015 genes participating in the development of primary sexual characteristics biological process from the curated GO Biological Process Annotations 2015 dataset. |
primary alcohol metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the primary alcohol metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
primary lung bud formation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the primary lung bud formation biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of primary metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of primary metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
primary amino compound metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the primary amino compound metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein localization to nonmotile primary cilium Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein localization to nonmotile primary cilium biological process from the curated GO Biological Process Annotations 2015 dataset. |
primary follicle stage Gene SetFrom GO Biological Process Annotations 2015 genes participating in the primary follicle stage biological process from the curated GO Biological Process Annotations 2015 dataset. |
primary alcohol catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the primary alcohol catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of nonmotile primary cilium assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of nonmotile primary cilium assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of nonmotile primary cilium assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of nonmotile primary cilium assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
cell fate commitment involved in formation of primary germ layer Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cell fate commitment involved in formation of primary germ layer biological process from the curated GO Biological Process Annotations 2015 dataset. |
primary prostatic bud elongation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the primary prostatic bud elongation biological process from the curated GO Biological Process Annotations 2015 dataset. |
primary sex determination, germ-line Gene SetFrom GO Biological Process Annotations 2015 genes participating in the primary sex determination, germ-line biological process from the curated GO Biological Process Annotations 2015 dataset. |
primary mirna processing Gene SetFrom GO Biological Process Annotations 2015 genes participating in the primary mirna processing biological process from the curated GO Biological Process Annotations 2015 dataset. |
primary heart field specification Gene SetFrom GO Biological Process Annotations 2015 genes participating in the primary heart field specification biological process from the curated GO Biological Process Annotations 2015 dataset. |
primary metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the primary metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of transcription involved in primary germ layer cell fate commitment Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of transcription involved in primary germ layer cell fate commitment biological process from the curated GO Biological Process Annotations 2015 dataset. |
primary spermatocyte growth Gene SetFrom GO Biological Process Annotations 2015 genes participating in the primary spermatocyte growth biological process from the curated GO Biological Process Annotations 2015 dataset. |
alveolar primary septum development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the alveolar primary septum development biological process from the curated GO Biological Process Annotations 2015 dataset. |
receptor localization to nonmotile primary cilium Gene SetFrom GO Biological Process Annotations 2015 genes participating in the receptor localization to nonmotile primary cilium biological process from the curated GO Biological Process Annotations 2015 dataset. |
primary alcohol biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the primary alcohol biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
nonmotile primary cilium assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the nonmotile primary cilium assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
primary sex determination Gene SetFrom GO Biological Process Annotations 2015 genes participating in the primary sex determination biological process from the curated GO Biological Process Annotations 2015 dataset. |
primary ovarian follicle growth Gene SetFrom GO Biological Process Annotations 2015 genes participating in the primary ovarian follicle growth biological process from the curated GO Biological Process Annotations 2015 dataset. |
primary amino compound biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the primary amino compound biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
formation of primary germ layer Gene SetFrom GO Biological Process Annotations 2015 genes participating in the formation of primary germ layer biological process from the curated GO Biological Process Annotations 2015 dataset. |
primary cilium Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the primary cilium cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
motile primary cilium Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the motile primary cilium cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
primary lysosome Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the primary lysosome cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
nonmotile primary cilium Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the nonmotile primary cilium cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
rrna primary transcript binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the rrna primary transcript binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
primary mirna binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the primary mirna binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
primary active transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the primary active transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
primary amine oxidase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the primary amine oxidase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Primary tooth development (number of teeth) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Primary tooth development (number of teeth) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Primary sclerosing cholangitis Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Primary sclerosing cholangitis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Glaucoma (primary open-angle) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Glaucoma (primary open-angle) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Primary biliary cirrhosis Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Primary biliary cirrhosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Primary tooth development (time to first tooth eruption) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Primary tooth development (time to first tooth eruption) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
primary bacterial infectious disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease primary bacterial infectious disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
primary biliary cirrhosis Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease primary biliary cirrhosis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
primary immunodeficiency disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease primary immunodeficiency disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
primary atrial arrhythmia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the primary atrial arrhythmia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
delayed eruption of primary teeth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the delayed eruption of primary teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of primary teeth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of primary teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
primary open angle glaucoma Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the primary open angle glaucoma phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
primary congenital glaucoma Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the primary congenital glaucoma phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
congenital primary aphakia Gene SetFrom HPO Gene-Disease Associations genes associated with the congenital primary aphakia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
primary ovarian failure Gene SetFrom HPO Gene-Disease Associations genes associated with the primary ovarian failure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of primary molar morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of primary molar morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the primary teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the primary teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
primary hypothyroidism Gene SetFrom HPO Gene-Disease Associations genes associated with the primary hypothyroidism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
unilateral primary pulmonary dysgenesis Gene SetFrom HPO Gene-Disease Associations genes associated with the unilateral primary pulmonary dysgenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
primary open angle glaucoma Gene SetFrom HPO Gene-Disease Associations genes associated with the primary open angle glaucoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of primary teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of primary teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
microdontia of primary teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the microdontia of primary teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
persistence of primary teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the persistence of primary teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
primary hyperparathyroidism Gene SetFrom HPO Gene-Disease Associations genes associated with the primary hyperparathyroidism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
primary gonadal insufficiency Gene SetFrom HPO Gene-Disease Associations genes associated with the primary gonadal insufficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
primary amenorrhea Gene SetFrom HPO Gene-Disease Associations genes associated with the primary amenorrhea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
primary congenital glaucoma Gene SetFrom HPO Gene-Disease Associations genes associated with the primary congenital glaucoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
premature loss of primary teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the premature loss of primary teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent primary metaphyseal spongiosa Gene SetFrom HPO Gene-Disease Associations genes associated with the absent primary metaphyseal spongiosa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
primary atrial arrhythmia Gene SetFrom HPO Gene-Disease Associations genes associated with the primary atrial arrhythmia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
primary hypercorticolism Gene SetFrom HPO Gene-Disease Associations genes associated with the primary hypercorticolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
persistent hyperplastic primary vitreous Gene SetFrom HPO Gene-Disease Associations genes associated with the persistent hyperplastic primary vitreous phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
delayed eruption of primary teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the delayed eruption of primary teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
primary adrenal insufficiency Gene SetFrom HPO Gene-Disease Associations genes associated with the primary adrenal insufficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Neoplasms, Second Primary Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Neoplasms, Second Primary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Primary Myelofibrosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Primary Myelofibrosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Primary Ovarian Insufficiency Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Primary Ovarian Insufficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Neoplasms, Unknown Primary Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Neoplasms, Unknown Primary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hyperoxaluria, Primary Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hyperoxaluria, Primary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Aphasia, Primary Progressive Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Aphasia, Primary Progressive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Primary Graft Dysfunction Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Primary Graft Dysfunction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Hyperparathyroidism, Primary Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Hyperparathyroidism, Primary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Neoplasms, Multiple Primary Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Neoplasms, Multiple Primary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Headache Disorders, Primary Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Headache Disorders, Primary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Myeloid differentiation primary response protein MyD88 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Myeloid differentiation primary response protein MyD88 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Primary ciliary dyskinesia protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Primary ciliary dyskinesia protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
abnormal primary sex determination Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal primary sex determination phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney epithelial cell primary cilium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney epithelial cell primary cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal renal tubule epithelial cell primary cilium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal renal tubule epithelial cell primary cilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal primary vitreous morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal primary vitreous morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lymph node primary follicle morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lymph node primary follicle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal primary ovarian follicle number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal primary ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal motile primary cilium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal motile primary cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal motile primary cilium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal motile primary cilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
cleft primary palate Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the cleft primary palate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent barrels in primary somatosensory cortex Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent barrels in primary somatosensory cortex phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal nonmotile primary cilium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal nonmotile primary cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cholangiocyte primary cilium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cholangiocyte primary cilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal spleen primary b follicle morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal spleen primary b follicle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
primary vitreous hyperplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the primary vitreous hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased primary ovarian follicle number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased primary ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal primary palate development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal primary palate development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
primary sex reversal Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the primary sex reversal phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal primary ovarian follicle morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal primary ovarian follicle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal nonmotile primary cilium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal nonmotile primary cilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal primary muscle spindle morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal primary muscle spindle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney epithelial cell primary cilium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney epithelial cell primary cilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent primary muscle spindle Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent primary muscle spindle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal primary polar body morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal primary polar body morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
primary atelectasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the primary atelectasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal primary cilium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal primary cilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal primary somatosensory cortex morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal primary somatosensory cortex morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
persistent hyperplastic primary vitreous Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the persistent hyperplastic primary vitreous phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal primary cilium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal primary cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
hyperoxaluria, primary, type iii Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyperoxaluria, primary, type iii phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyperparathyroidism, familial primary Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyperparathyroidism, familial primary phenotype from the curated OMIM Gene-Disease Associations dataset. |
dystonia-17, primary torsion Gene SetFrom OMIM Gene-Disease Associations genes associated with the dystonia-17, primary torsion phenotype from the curated OMIM Gene-Disease Associations dataset. |
glaucoma 1b, primary open angle, adult onset, Gene SetFrom OMIM Gene-Disease Associations genes associated with the glaucoma 1b, primary open angle, adult onset, phenotype from the curated OMIM Gene-Disease Associations dataset. |
pulmonary hypertension, primary, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the pulmonary hypertension, primary, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
pulmonary hypertension, primary, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the pulmonary hypertension, primary, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
pulmonary hypertension, primary, fenfluramine or dexfenfluramine-associated Gene SetFrom OMIM Gene-Disease Associations genes associated with the pulmonary hypertension, primary, fenfluramine or dexfenfluramine-associated phenotype from the curated OMIM Gene-Disease Associations dataset. |
?microcephaly 11, primary, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?microcephaly 11, primary, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
cholangitis, primary sclerosing Gene SetFrom OMIM Gene-Disease Associations genes associated with the cholangitis, primary sclerosing phenotype from the curated OMIM Gene-Disease Associations dataset. |
{biliary cirrhosis, primary, 3} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {biliary cirrhosis, primary, 3} phenotype from the curated OMIM Gene-Disease Associations dataset. |
glaucoma 1a, primary open angle Gene SetFrom OMIM Gene-Disease Associations genes associated with the glaucoma 1a, primary open angle phenotype from the curated OMIM Gene-Disease Associations dataset. |
microcephaly 2, primary, autosomal recessive, with or without cortical malformations Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcephaly 2, primary, autosomal recessive, with or without cortical malformations phenotype from the curated OMIM Gene-Disease Associations dataset. |
ciliary dyskinesia, primary, 28 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 28 phenotype from the curated OMIM Gene-Disease Associations dataset. |
microcephaly 5, primary, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcephaly 5, primary, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
ciliary dyskinesia, primary, 22 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 22 phenotype from the curated OMIM Gene-Disease Associations dataset. |
ciliary dyskinesia, primary, 23 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 23 phenotype from the curated OMIM Gene-Disease Associations dataset. |
ciliary dyskinesia, primary, 20 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 20 phenotype from the curated OMIM Gene-Disease Associations dataset. |
ciliary dyskinesia, primary, 21 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 21 phenotype from the curated OMIM Gene-Disease Associations dataset. |
ciliary dyskinesia, primary, 26 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 26 phenotype from the curated OMIM Gene-Disease Associations dataset. |
ciliary dyskinesia, primary, 27 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 27 phenotype from the curated OMIM Gene-Disease Associations dataset. |
ciliary dyskinesia, primary, 24 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 24 phenotype from the curated OMIM Gene-Disease Associations dataset. |
ciliary dyskinesia, primary, 25 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 25 phenotype from the curated OMIM Gene-Disease Associations dataset. |
ciliary dyskinesia, primary, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyperoxaluria, primary, type ii Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyperoxaluria, primary, type ii phenotype from the curated OMIM Gene-Disease Associations dataset. |
bile acid malabsorption, primary Gene SetFrom OMIM Gene-Disease Associations genes associated with the bile acid malabsorption, primary phenotype from the curated OMIM Gene-Disease Associations dataset. |
biliary cirrhosis, primary, 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the biliary cirrhosis, primary, 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
biliary cirrhosis, primary, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the biliary cirrhosis, primary, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
primary lateral sclerosis, juvenile Gene SetFrom OMIM Gene-Disease Associations genes associated with the primary lateral sclerosis, juvenile phenotype from the curated OMIM Gene-Disease Associations dataset. |
glaucoma 3, primary congenital, d Gene SetFrom OMIM Gene-Disease Associations genes associated with the glaucoma 3, primary congenital, d phenotype from the curated OMIM Gene-Disease Associations dataset. |
glaucoma 3, primary congenital, c Gene SetFrom OMIM Gene-Disease Associations genes associated with the glaucoma 3, primary congenital, c phenotype from the curated OMIM Gene-Disease Associations dataset. |
microcephaly 9, primary, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcephaly 9, primary, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
dystonia, primary cervical Gene SetFrom OMIM Gene-Disease Associations genes associated with the dystonia, primary cervical phenotype from the curated OMIM Gene-Disease Associations dataset. |
hyperoxaluria, primary, type 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the hyperoxaluria, primary, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
primary aldosteronism, seizures, and neurologic abnormalities Gene SetFrom OMIM Gene-Disease Associations genes associated with the primary aldosteronism, seizures, and neurologic abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset. |
hypertrophic osteoarthropathy, primary, autosomal recessive 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypertrophic osteoarthropathy, primary, autosomal recessive 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
hypertrophic osteoarthropathy, primary, autosomal recessive 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypertrophic osteoarthropathy, primary, autosomal recessive 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
aphakia, congenital primary Gene SetFrom OMIM Gene-Disease Associations genes associated with the aphakia, congenital primary phenotype from the curated OMIM Gene-Disease Associations dataset. |
pulmonary hypertension, primary, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the pulmonary hypertension, primary, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
microcephaly 6, primary, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcephaly 6, primary, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
pulmonary hypertension, familial primary, 1, with or without hht Gene SetFrom OMIM Gene-Disease Associations genes associated with the pulmonary hypertension, familial primary, 1, with or without hht phenotype from the curated OMIM Gene-Disease Associations dataset. |
failure of tooth eruption, primary Gene SetFrom OMIM Gene-Disease Associations genes associated with the failure of tooth eruption, primary phenotype from the curated OMIM Gene-Disease Associations dataset. |
microcephaly 1, primary, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcephaly 1, primary, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
?microcephaly 8, primary, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?microcephaly 8, primary, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
erythermalgia, primary Gene SetFrom OMIM Gene-Disease Associations genes associated with the erythermalgia, primary phenotype from the curated OMIM Gene-Disease Associations dataset. |
aphasia, primary progressive Gene SetFrom OMIM Gene-Disease Associations genes associated with the aphasia, primary progressive phenotype from the curated OMIM Gene-Disease Associations dataset. |
pigmented nodular adrenocortical disease, primary, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the pigmented nodular adrenocortical disease, primary, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
pigmented nodular adrenocortical disease, primary, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the pigmented nodular adrenocortical disease, primary, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
pigmented nodular adrenocortical disease, primary, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the pigmented nodular adrenocortical disease, primary, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
glaucoma 1c, primary open angle Gene SetFrom OMIM Gene-Disease Associations genes associated with the glaucoma 1c, primary open angle phenotype from the curated OMIM Gene-Disease Associations dataset. |
immunodeficiency, primary, autosomal recessive, il21r-related Gene SetFrom OMIM Gene-Disease Associations genes associated with the immunodeficiency, primary, autosomal recessive, il21r-related phenotype from the curated OMIM Gene-Disease Associations dataset. |
ciliary dyskinesia, primary, 9, with or without situs inversus Gene SetFrom OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 9, with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset. |
primary lateral sclerosis, adult, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the primary lateral sclerosis, adult, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
ciliary dyskinesia, primary, 13 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 13 phenotype from the curated OMIM Gene-Disease Associations dataset. |
ciliary dyskinesia, primary, 12 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 12 phenotype from the curated OMIM Gene-Disease Associations dataset. |
ciliary dyskinesia, primary, 11 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 11 phenotype from the curated OMIM Gene-Disease Associations dataset. |
ciliary dyskinesia, primary, 10 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 10 phenotype from the curated OMIM Gene-Disease Associations dataset. |
ciliary dyskinesia, primary, 17 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 17 phenotype from the curated OMIM Gene-Disease Associations dataset. |
ciliary dyskinesia, primary, 16 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 16 phenotype from the curated OMIM Gene-Disease Associations dataset. |
ciliary dyskinesia, primary, 15 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 15 phenotype from the curated OMIM Gene-Disease Associations dataset. |
ciliary dyskinesia, primary, 14 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 14 phenotype from the curated OMIM Gene-Disease Associations dataset. |
ciliary dyskinesia, primary, 19 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 19 phenotype from the curated OMIM Gene-Disease Associations dataset. |
ciliary dyskinesia, primary, 18 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 18 phenotype from the curated OMIM Gene-Disease Associations dataset. |
microcephaly 3, primary, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcephaly 3, primary, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
amyloidosis, primary localized cutaneous, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the amyloidosis, primary localized cutaneous, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
amyloidosis, primary localized cutaneous, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the amyloidosis, primary localized cutaneous, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
{biliary cirrhosis, primary, 2} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {biliary cirrhosis, primary, 2} phenotype from the curated OMIM Gene-Disease Associations dataset. |
ciliary dyskinesia, primary, 7, with or without situs inversus Gene SetFrom OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 7, with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset. |
glaucoma 1k, primary open angle, juvenile-onset Gene SetFrom OMIM Gene-Disease Associations genes associated with the glaucoma 1k, primary open angle, juvenile-onset phenotype from the curated OMIM Gene-Disease Associations dataset. |
ciliary dyskinesia, primary, 1, with or without situs inversus Gene SetFrom OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 1, with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset. |
glaucoma 3a, primary open angle, congenital, juvenile, or adult onset Gene SetFrom OMIM Gene-Disease Associations genes associated with the glaucoma 3a, primary open angle, congenital, juvenile, or adult onset phenotype from the curated OMIM Gene-Disease Associations dataset. |
microcephaly 4, primary, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcephaly 4, primary, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
ciliary dyskinesia, primary, 30 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 30 phenotype from the curated OMIM Gene-Disease Associations dataset. |
pneumothorax, primary spontaneous Gene SetFrom OMIM Gene-Disease Associations genes associated with the pneumothorax, primary spontaneous phenotype from the curated OMIM Gene-Disease Associations dataset. |
ciliary dyskinesia, primary, 8 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 8 phenotype from the curated OMIM Gene-Disease Associations dataset. |
ciliary dyskinesia, primary, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
ciliary dyskinesia, primary, 6 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 6 phenotype from the curated OMIM Gene-Disease Associations dataset. |
ciliary dyskinesia, primary, 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
glaucoma 1d, primary open angle Gene SetFrom OMIM Gene-Disease Associations genes associated with the glaucoma 1d, primary open angle phenotype from the curated OMIM Gene-Disease Associations dataset. |
?microcephaly 12, primary, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?microcephaly 12, primary, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
microcephaly 7, primary, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the microcephaly 7, primary, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
?microcephaly 13, primary, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?microcephaly 13, primary, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
ciliary dyskinesia, primary, 3, with or without situs inversus Gene SetFrom OMIM Gene-Disease Associations genes associated with the ciliary dyskinesia, primary, 3, with or without situs inversus phenotype from the curated OMIM Gene-Disease Associations dataset. |
pigmented nodular adrenocortical disease, primary, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the pigmented nodular adrenocortical disease, primary, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
ciliary diskinesia, primary, 29 Gene SetFrom OMIM Gene-Disease Associations genes associated with the ciliary diskinesia, primary, 29 phenotype from the curated OMIM Gene-Disease Associations dataset. |
?microcephaly 10, primary, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?microcephaly 10, primary, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
{blepharospasm, primary benign} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {blepharospasm, primary benign} phenotype from the curated OMIM Gene-Disease Associations dataset. |
glaucoma 3, primary infantile, b Gene SetFrom OMIM Gene-Disease Associations genes associated with the glaucoma 3, primary infantile, b phenotype from the curated OMIM Gene-Disease Associations dataset. |
persistent hyperplastic primary vitreous, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the persistent hyperplastic primary vitreous, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
Assembly of the primary cilium Gene Setproteins participating in the Assembly of the primary cilium pathway from the Reactome Pathways dataset. |
Primary B cells from cord blood Gene SetFrom Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles genes with high or low DNA methylation in Primary B cells from cord blood relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset. |
Primary hematopoietic stem cells G-CSF-mobilized Female RO_01508 Gene SetFrom Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles genes with high or low DNA methylation in Primary hematopoietic stem cells G-CSF-mobilized Female RO_01508 relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset. |
Primary hematopoietic stem cells G-CSF-mobilized Female RO_01549 Gene SetFrom Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles genes with high or low DNA methylation in Primary hematopoietic stem cells G-CSF-mobilized Female RO_01549 relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset. |
Primary T cells from cord blood Gene SetFrom Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles genes with high or low DNA methylation in Primary T cells from cord blood relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset. |
Primary hematopoietic stem cells G-CSF-mobilized Female RO_01480 Gene SetFrom Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles genes with high or low DNA methylation in Primary hematopoietic stem cells G-CSF-mobilized Female RO_01480 relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset. |
Primary hematopoietic stem cells Gene SetFrom Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles genes with high or low DNA methylation in Primary hematopoietic stem cells relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset. |
Primary hematopoietic stem cells G-CSF-mobilized Female RO_01536 Gene SetFrom Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles genes with high or low DNA methylation in Primary hematopoietic stem cells G-CSF-mobilized Female RO_01536 relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset. |
Primary hematopoietic stem cells G-CSF-mobilized Male Gene SetFrom Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles genes with high or low DNA methylation in Primary hematopoietic stem cells G-CSF-mobilized Male relative to other cell types and tissues from the Roadmap Epigenomics Cell and Tissue DNA Methylation Profiles dataset. |
H3K36me3_CD19 Primary Cells Gene SetFrom Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K36me3_CD19 Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset. |
H3K9me3_Peripheral Blood Mononuclear Primary Cells Gene SetFrom Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K9me3_Peripheral Blood Mononuclear Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset. |
H3K27me3_CD4 Memory Primary Cells Gene SetFrom Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K27me3_CD4 Memory Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset. |
H3K36me3_Treg Primary Cells Gene SetFrom Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K36me3_Treg Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset. |
H3K27ac_CD8 Naive Primary Cells Gene SetFrom Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K27ac_CD8 Naive Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset. |
H3K27ac_CD4+ CD25int CD127+ Tmem Primary Cells Gene SetFrom Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K27ac_CD4+ CD25int CD127+ Tmem Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset. |
H3K36me3_CD4+ CD25- CD45RA+ Naive Primary Cells Gene SetFrom Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K36me3_CD4+ CD25- CD45RA+ Naive Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset. |
H3K9me3_CD4+ CD25+ CD127- Treg Primary Cells Gene SetFrom Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K9me3_CD4+ CD25+ CD127- Treg Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset. |
H3K4me1_CD4+ CD25- IL17+ PMA-Ionomcyin stimulated Th17 Primary Cells Gene SetFrom Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K4me1_CD4+ CD25- IL17+ PMA-Ionomcyin stimulated Th17 Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset. |
H3K27ac_CD4+ CD25- IL17+ PMA-Ionomcyin stimulated Th17 Primary Cells Gene SetFrom Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K27ac_CD4+ CD25- IL17+ PMA-Ionomcyin stimulated Th17 Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset. |
H3K27ac_CD4+ CD25- CD45RA+ Naive Primary Cells Gene SetFrom Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K27ac_CD4+ CD25- CD45RA+ Naive Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset. |
H3K9ac_Peripheral Blood Mononuclear Primary Cells Gene SetFrom Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K9ac_Peripheral Blood Mononuclear Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset. |
H3K4me3_CD19 Primary Cells Gene SetFrom Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K4me3_CD19 Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset. |
H3K27me3_Treg Primary Cells Gene SetFrom Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K27me3_Treg Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset. |
H3K36me3_CD4+ CD25- IL17+ PMA-Ionomcyin stimulated Th17 Primary Cells Gene SetFrom Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K36me3_CD4+ CD25- IL17+ PMA-Ionomcyin stimulated Th17 Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset. |
H3K27ac_CD4 Memory Primary Cells Gene SetFrom Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K27ac_CD4 Memory Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset. |
H3K36me3_CD34 Primary Cells Gene SetFrom Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K36me3_CD34 Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset. |
H3K4me3_Mobilized CD34 Primary Cells Gene SetFrom Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K4me3_Mobilized CD34 Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset. |
H3K4me3_CD4+ CD25+ CD127- Treg Primary Cells Gene SetFrom Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K4me3_CD4+ CD25+ CD127- Treg Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset. |
H3K4me1_CD8 Naive Primary Cells Gene SetFrom Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K4me1_CD8 Naive Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset. |
H3K9ac_Penis Foreskin Keratinocyte Primary Cells Gene SetFrom Roadmap Epigenomics Histone Modification Site Profiles genes with high histone modification abundance in the H3K9ac_Penis Foreskin Keratinocyte Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset. |