7q11 23 distal copy number variation

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Results for "7q11 23 distal copy number variation": 1001 gene sets

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7q11 23 distal copy number variation Gene Set From WikiPathways Pathways 2024 proteins participating in the 7q11 23 distal copy number variation pathway from the WikiPathways Pathways 2024 dataset.
7q11 23 copy number variation syndrome Gene Set From WikiPathways Pathways 2024 proteins participating in the 7q11 23 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.
22q11 2 copy number variation syndrome Gene Set From WikiPathways Pathways 2024 proteins participating in the 22q11 2 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.
1q21 1 copy number variation syndrome Gene Set From WikiPathways Pathways 2024 proteins participating in the 1q21 1 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.
3q29 copy number variation syndrome Gene Set From WikiPathways Pathways 2024 proteins participating in the 3q29 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.
15q11 2 copy number variation syndrome Gene Set From WikiPathways Pathways 2024 proteins participating in the 15q11 2 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.
15q13 3 copy number variation syndrome Gene Set From WikiPathways Pathways 2024 proteins participating in the 15q13 3 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.
2q11 2 copy number variation syndrome Gene Set From WikiPathways Pathways 2024 proteins participating in the 2q11 2 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.
2q13 copy number variation syndrome Gene Set From WikiPathways Pathways 2024 proteins participating in the 2q13 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.
2q21 1 copy number variation syndrome Gene Set From WikiPathways Pathways 2024 proteins participating in the 2q21 1 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.
2q37 copy number variation syndrome Gene Set From WikiPathways Pathways 2024 proteins participating in the 2q37 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.
17q12 copy number variation syndrome Gene Set From WikiPathways Pathways 2024 proteins participating in the 17q12 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.
1p36 copy number variation syndrome Gene Set From WikiPathways Pathways 2024 proteins participating in the 1p36 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.
8p23 1 copy number variation syndrome Gene Set From WikiPathways Pathways 2024 proteins participating in the 8p23 1 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.
11p11 2 copy number variation syndrome Gene Set From WikiPathways Pathways 2024 proteins participating in the 11p11 2 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.
10q11 21q11 23 copy number variation syndrome Gene Set From WikiPathways Pathways 2024 proteins participating in the 10q11 21q11 23 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.
4p16 3 copy number variation Gene Set From WikiPathways Pathways 2024 proteins participating in the 4p16 3 copy number variation pathway from the WikiPathways Pathways 2024 dataset.
NF1 copy number variation syndrome Gene Set From WikiPathways Pathways 2024 proteins participating in the NF1 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.
17p13 3 YWHAE copy number variation Gene Set From WikiPathways Pathways 2024 proteins participating in the 17p13 3 YWHAE copy number variation pathway from the WikiPathways Pathways 2024 dataset.
5q35 copy number variation Gene Set From WikiPathways Pathways 2024 proteins participating in the 5q35 copy number variation pathway from the WikiPathways Pathways 2024 dataset.
Smith Magenis and Potocki Lupski syndrome copy number variation Gene Set From WikiPathways Pathways 2024 proteins participating in the Smith Magenis and Potocki Lupski syndrome copy number variation pathway from the WikiPathways Pathways 2024 dataset.
6q16 copy number variation Gene Set From WikiPathways Pathways 2024 proteins participating in the 6q16 copy number variation pathway from the WikiPathways Pathways 2024 dataset.
10q22q23 copy number variation Gene Set From WikiPathways Pathways 2024 proteins participating in the 10q22q23 copy number variation pathway from the WikiPathways Pathways 2024 dataset.
13q12 or CRYL1 copy number variation Gene Set From WikiPathways Pathways 2024 proteins participating in the 13q12 or CRYL1 copy number variation pathway from the WikiPathways Pathways 2024 dataset.
13q12 12 copy number variation Gene Set From WikiPathways Pathways 2024 proteins participating in the 13q12 12 copy number variation pathway from the WikiPathways Pathways 2024 dataset.
15q11q13 copy number variation Gene Set From WikiPathways Pathways 2024 proteins participating in the 15q11q13 copy number variation pathway from the WikiPathways Pathways 2024 dataset.
15q25 copy number variation Gene Set From WikiPathways Pathways 2024 proteins participating in the 15q25 copy number variation pathway from the WikiPathways Pathways 2024 dataset.
PAFAH1B1 copy number variation Gene Set From WikiPathways Pathways 2024 proteins participating in the PAFAH1B1 copy number variation pathway from the WikiPathways Pathways 2024 dataset.
8q11 23 RB1CC1 copy number variation Gene Set From WikiPathways Pathways 2024 proteins participating in the 8q11 23 RB1CC1 copy number variation pathway from the WikiPathways Pathways 2024 dataset.
chromosome 7q11.23 deletion syndrome, distal, 1.2mb Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 7q11.23 deletion syndrome, distal, 1.2mb phenotype from the curated OMIM Gene-Disease Associations dataset.
Mitochondrial DNA copy number (white blood cells) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mitochondrial DNA copy number (white blood cells) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Mitochondrial DNA copy number Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Mitochondrial DNA copy number phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Epstein-Barr virus copy number in lymphoblastoid cell lines Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Epstein-Barr virus copy number in lymphoblastoid cell lines phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
chromosome 7q11.23 duplication syndrome Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 7q11.23 duplication syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
7q11.23 duplication syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease 7q11.23 duplication syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
7q11.23 duplication syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease 7q11.23 duplication syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
copy Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term copy in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Impdh2 enzyme activity, variation in Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Impdh2 enzyme activity, variation in phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Skin/hair/eye pigmentation, variation in, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Skin/hair/eye pigmentation, variation in, 8 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Skin/hair/eye pigmentation, variation in, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Skin/hair/eye pigmentation, variation in, 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Skin/hair/eye pigmentation, variation in, 9 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Skin/hair/eye pigmentation, variation in, 10 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Skin/hair/eye pigmentation, variation in, 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Apocrine gland secretion, variation in Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Apocrine gland secretion, variation in phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
QT INTERVAL, VARIATION IN Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease QT INTERVAL, VARIATION IN from the curated CTD Gene-Disease Associations dataset.
quantitative variation in lipid and lipoprotein traits Gene Set From GAD Gene-Disease Associations genes associated with the disease quantitative variation in lipid and lipoprotein traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
normmal variation Gene Set From GAD Gene-Disease Associations genes associated with the disease normmal variation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
normal variation in leptin levels Gene Set From GAD Gene-Disease Associations genes associated with the disease normal variation in leptin levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nomal variation Gene Set From GAD Gene-Disease Associations genes associated with the disease nomal variation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pharmacogenetic variation Gene Set From GAD Gene-Disease Associations genes associated with the disease pharmacogenetic variation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dyslexia; reading; normal variation Gene Set From GAD Gene-Disease Associations genes associated with the disease dyslexia; reading; normal variation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
variation in platelet integrin alpha 2 beta 1 density Gene Set From GAD Gene-Disease Associations genes associated with the disease variation in platelet integrin alpha 2 beta 1 density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
variation in plasma lipoproteins Gene Set From GAD Gene-Disease Associations genes associated with the disease variation in plasma lipoproteins in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
quantitative variation in plasma high-density lipoproteins and triacylglycerides Gene Set From GAD Gene-Disease Associations genes associated with the disease quantitative variation in plasma high-density lipoproteins and triacylglycerides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
normal variation Gene Set From GAD Gene-Disease Associations genes associated with the disease normal variation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
variation Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term variation in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
DNA methylation (variation) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the DNA methylation (variation) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
patchy variation in bone mineral density Gene Set From HPO Gene-Disease Associations genes associated with the patchy variation in bone mineral density phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
[skin/hair/eye pigmentation, variation in, 8] Gene Set From OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation, variation in, 8] phenotype from the curated OMIM Gene-Disease Associations dataset.
[axillary odor, variation in] Gene Set From OMIM Gene-Disease Associations genes associated with the [axillary odor, variation in] phenotype from the curated OMIM Gene-Disease Associations dataset.
[colostrum secretion, variation in] Gene Set From OMIM Gene-Disease Associations genes associated with the [colostrum secretion, variation in] phenotype from the curated OMIM Gene-Disease Associations dataset.
[skin/hair/eye pigmentation, variation in, 11 (melanesian blond hair)] Gene Set From OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation, variation in, 11 (melanesian blond hair)] phenotype from the curated OMIM Gene-Disease Associations dataset.
[qt interval, variation in] Gene Set From OMIM Gene-Disease Associations genes associated with the [qt interval, variation in] phenotype from the curated OMIM Gene-Disease Associations dataset.
{gene expression, variation in, qtl} Gene Set From OMIM Gene-Disease Associations genes associated with the {gene expression, variation in, qtl} phenotype from the curated OMIM Gene-Disease Associations dataset.
[impdh2 enzyme activity, variation in] Gene Set From OMIM Gene-Disease Associations genes associated with the [impdh2 enzyme activity, variation in] phenotype from the curated OMIM Gene-Disease Associations dataset.
[bone mineral density variation qtl] Gene Set From OMIM Gene-Disease Associations genes associated with the [bone mineral density variation qtl] phenotype from the curated OMIM Gene-Disease Associations dataset.
{obesity, variation in} Gene Set From OMIM Gene-Disease Associations genes associated with the {obesity, variation in} phenotype from the curated OMIM Gene-Disease Associations dataset.
Impdh2 Enzyme Activity, Variation In Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Impdh2 Enzyme Activity, Variation In in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Patchy Variation In Bone Mineral Density Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Patchy Variation In Bone Mineral Density in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Myopathy caused by variation in F Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Myopathy caused by variation in F phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Myopathy caused by variation in POMG Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Myopathy caused by variation in POMG phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Myopathy caused by variation in PO Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Myopathy caused by variation in PO phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
DNA methylation (variation) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the DNA methylation (variation) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Distal hereditary motor neuronopathy 2D Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal tubular acidosis, distal, autosomal dominant Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal tubular acidosis, distal, autosomal recessive Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distal spinal muscular atrophy, X-linked 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal spinal muscular atrophy, X-linked 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal tubular acidosis, distal, with normal red cell morphology Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, with normal red cell morphology phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distal hereditary motor neuronopathy type 2A Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distal hereditary motor neuronopathy type 2C Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distal hereditary motor neuronopathy type 2B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distal myopathy Markesbery-Griggs type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal myopathy Markesbery-Griggs type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, distal, 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, distal, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distal hereditary motor neuronopathy type 5B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 5B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distal arthrogryposis type 1B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal arthrogryposis type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distal hereditary motor neuronopathy type 7B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 7B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal tubular acidosis, distal, with hemolytic anemia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, with hemolytic anemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distal hereditary motor neuronopathy type 5 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distal arthrogryposis type 2B Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal arthrogryposis type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Arthrogryposis, distal, type 5d Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, distal, type 5d phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, distal, 1 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, distal, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, distal, 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopathy, distal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Distal spinal muscular atrophy, autosomal recessive 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Distal spinal muscular atrophy, autosomal recessive 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopathy, Distal, with Anterior Tibial Onset Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Distal, with Anterior Tibial Onset from the curated CTD Gene-Disease Associations dataset.
Welander distal myopathy, Swedish type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Welander distal myopathy, Swedish type from the curated CTD Gene-Disease Associations dataset.
Neuropathy, Distal Hereditary Motor, Type IIA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Distal Hereditary Motor, Type IIA from the curated CTD Gene-Disease Associations dataset.
Renal Tubular Acidosis, Distal, With Hemolytic Anemia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal Tubular Acidosis, Distal, With Hemolytic Anemia from the curated CTD Gene-Disease Associations dataset.
Neuronopathy, Distal Hereditary Motor, Type V Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuronopathy, Distal Hereditary Motor, Type V from the curated CTD Gene-Disease Associations dataset.
Jacobsen Distal 11q Deletion Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Jacobsen Distal 11q Deletion Syndrome from the curated CTD Gene-Disease Associations dataset.
Renal tubular acidosis, distal, autosomal recessive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal tubular acidosis, distal, autosomal recessive from the curated CTD Gene-Disease Associations dataset.
Neuronopathy, Distal Hereditary Motor, Type IIB Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuronopathy, Distal Hereditary Motor, Type IIB from the curated CTD Gene-Disease Associations dataset.
Arthrogryposis, Distal, Type 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arthrogryposis, Distal, Type 4 from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 from the curated CTD Gene-Disease Associations dataset.
ARTHROGRYPOSIS, DISTAL, TYPE 1A Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease ARTHROGRYPOSIS, DISTAL, TYPE 1A from the curated CTD Gene-Disease Associations dataset.
Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness from the curated CTD Gene-Disease Associations dataset.
Distal myopathy, Nonaka type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Distal myopathy, Nonaka type from the curated CTD Gene-Disease Associations dataset.
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC from the curated CTD Gene-Disease Associations dataset.
Neuropathy, Distal Hereditary Motor, Type VIIA Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Distal Hereditary Motor, Type VIIA from the curated CTD Gene-Disease Associations dataset.
Arthrogryposis multiplex congenita, distal, X-linked Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Arthrogryposis multiplex congenita, distal, X-linked from the curated CTD Gene-Disease Associations dataset.
Distal Myopathies Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Distal Myopathies from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Distal, Congenital Nonprogressive Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Congenital Nonprogressive from the curated CTD Gene-Disease Associations dataset.
Neuronopathy, Distal Hereditary Motor, Type Viib Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Neuronopathy, Distal Hereditary Motor, Type Viib from the curated CTD Gene-Disease Associations dataset.
Spinal Muscular Atrophy, Distal, X-Linked 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, X-Linked 3 from the curated CTD Gene-Disease Associations dataset.
Distal arthrogryposis type 2B Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Distal arthrogryposis type 2B from the curated CTD Gene-Disease Associations dataset.
distal muscular dystrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease distal muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
distal hereditary motor neuropathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease distal hereditary motor neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
distal arthrogryposis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease distal arthrogryposis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
familial distal renal tubular acidosis Gene Set From GAD Gene-Disease Associations genes associated with the disease familial distal renal tubular acidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
proximal chromosome 9p to q and distal chromosome 9q Gene Set From GAD Gene-Disease Associations genes associated with the disease proximal chromosome 9p to q and distal chromosome 9q in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
distal myopathies; myositis, inclusion body Gene Set From GAD Gene-Disease Associations genes associated with the disease distal myopathies; myositis, inclusion body in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
distal Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term distal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
proximal/distal pattern formation involved in nephron development Gene Set From GO Biological Process Annotations 2015 genes participating in the proximal/distal pattern formation involved in nephron development biological process from the curated GO Biological Process Annotations 2015 dataset.
metanephric distal convoluted tubule development Gene Set From GO Biological Process Annotations 2015 genes participating in the metanephric distal convoluted tubule development biological process from the curated GO Biological Process Annotations 2015 dataset.
proximal/distal pattern formation involved in metanephric nephron development Gene Set From GO Biological Process Annotations 2015 genes participating in the proximal/distal pattern formation involved in metanephric nephron development biological process from the curated GO Biological Process Annotations 2015 dataset.
metanephric distal tubule development Gene Set From GO Biological Process Annotations 2015 genes participating in the metanephric distal tubule development biological process from the curated GO Biological Process Annotations 2015 dataset.
metanephric distal tubule morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the metanephric distal tubule morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
distal tubule morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the distal tubule morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
distal tubule development Gene Set From GO Biological Process Annotations 2015 genes participating in the distal tubule development biological process from the curated GO Biological Process Annotations 2015 dataset.
lung proximal/distal axis specification Gene Set From GO Biological Process Annotations 2015 genes participating in the lung proximal/distal axis specification biological process from the curated GO Biological Process Annotations 2015 dataset.
polarity specification of proximal/distal axis Gene Set From GO Biological Process Annotations 2015 genes participating in the polarity specification of proximal/distal axis biological process from the curated GO Biological Process Annotations 2015 dataset.
proximal/distal axis specification Gene Set From GO Biological Process Annotations 2015 genes participating in the proximal/distal axis specification biological process from the curated GO Biological Process Annotations 2015 dataset.
proximal/distal pattern formation Gene Set From GO Biological Process Annotations 2015 genes participating in the proximal/distal pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset.
distal convoluted tubule development Gene Set From GO Biological Process Annotations 2015 genes participating in the distal convoluted tubule development biological process from the curated GO Biological Process Annotations 2015 dataset.
rna polymerase ii distal enhancer sequence-specific dna binding transcription factor activity involved in positive regulation of transcription Gene Set From GO Molecular Function Annotations 2015 genes performing the rna polymerase ii distal enhancer sequence-specific dna binding transcription factor activity involved in positive regulation of transcription molecular function from the curated GO Molecular Function Annotations 2015 dataset.
rna polymerase ii distal enhancer sequence-specific dna binding transcription factor activity Gene Set From GO Molecular Function Annotations 2015 genes performing the rna polymerase ii distal enhancer sequence-specific dna binding transcription factor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
rna polymerase ii distal enhancer sequence-specific dna binding Gene Set From GO Molecular Function Annotations 2015 genes performing the rna polymerase ii distal enhancer sequence-specific dna binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
rna polymerase ii distal enhancer sequence-specific dna binding transcription factor activity involved in negative regulation of transcription Gene Set From GO Molecular Function Annotations 2015 genes performing the rna polymerase ii distal enhancer sequence-specific dna binding transcription factor activity involved in negative regulation of transcription molecular function from the curated GO Molecular Function Annotations 2015 dataset.
wide tufts of distal phalanges Gene Set From HPO Gene-Disease Associations genes associated with the wide tufts of distal phalanges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
tapering pointed ends of distal finger phalanges Gene Set From HPO Gene-Disease Associations genes associated with the tapering pointed ends of distal finger phalanges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short distal phalanx of finger Gene Set From HPO Gene-Disease Associations genes associated with the short distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the distal phalanx of the 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal upper limb muscle weakness Gene Set From HPO Gene-Disease Associations genes associated with the distal upper limb muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
osteolytic defects of the distal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the osteolytic defects of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the distal phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal widening of metacarpals Gene Set From HPO Gene-Disease Associations genes associated with the distal widening of metacarpals phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
late-onset distal muscle weakness Gene Set From HPO Gene-Disease Associations genes associated with the late-onset distal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the distal phalanx of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
impaired distal vibration sensation Gene Set From HPO Gene-Disease Associations genes associated with the impaired distal vibration sensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
broad distal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the broad distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of distal phalanx of toe Gene Set From HPO Gene-Disease Associations genes associated with the duplication of distal phalanx of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
partial duplication of the distal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the partial duplication of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
impaired distal tactile sensation Gene Set From HPO Gene-Disease Associations genes associated with the impaired distal tactile sensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of the distal phalanx of hand Gene Set From HPO Gene-Disease Associations genes associated with the duplication of the distal phalanx of hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the epiphyses of the distal phalanx of finger Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
broad distal phalanges of all fingers Gene Set From HPO Gene-Disease Associations genes associated with the broad distal phalanges of all fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of the distal phalanx of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the duplication of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
sclerosis of distal finger phalanx Gene Set From HPO Gene-Disease Associations genes associated with the sclerosis of distal finger phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the distal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the distal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
trapezoidal distal femoral condyles Gene Set From HPO Gene-Disease Associations genes associated with the trapezoidal distal femoral condyles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
partial duplication of the distal phalanx of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the partial duplication of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
dysplastic distal thumb phalanges with a central hole Gene Set From HPO Gene-Disease Associations genes associated with the dysplastic distal thumb phalanges with a central hole phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
widened distal phalanges Gene Set From HPO Gene-Disease Associations genes associated with the widened distal phalanges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the distal femoral epiphysis Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the distal femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
small distal femoral epiphysis Gene Set From HPO Gene-Disease Associations genes associated with the small distal femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the distal phalanges of the toes Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
osteomyelitis or necrosis, distal, due to sensory neuropathy (feet) Gene Set From HPO Gene-Disease Associations genes associated with the osteomyelitis or necrosis, distal, due to sensory neuropathy (feet) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
partial duplication of the distal phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the partial duplication of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
broad distal hallux Gene Set From HPO Gene-Disease Associations genes associated with the broad distal hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absent distal interphalangeal creases Gene Set From HPO Gene-Disease Associations genes associated with the absent distal interphalangeal creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
triangular shaped distal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the triangular shaped distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
slender distal phalanx of finger Gene Set From HPO Gene-Disease Associations genes associated with the slender distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
broad distal phalanx of finger Gene Set From HPO Gene-Disease Associations genes associated with the broad distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the distal phalanx of the 4th finger Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal ulnar hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the distal ulnar hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short distal phalanx of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the short distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive distal muscular atrophy Gene Set From HPO Gene-Disease Associations genes associated with the progressive distal muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal upper limb amyotrophy Gene Set From HPO Gene-Disease Associations genes associated with the distal upper limb amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
bifid distal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the bifid distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal lower limb amyotrophy Gene Set From HPO Gene-Disease Associations genes associated with the distal lower limb amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal lower limb muscle weakness Gene Set From HPO Gene-Disease Associations genes associated with the distal lower limb muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased distal sensory nerve action potential Gene Set From HPO Gene-Disease Associations genes associated with the decreased distal sensory nerve action potential phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the distal phalanx of the 4th finger Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal femoral metaphyseal abnormality Gene Set From HPO Gene-Disease Associations genes associated with the distal femoral metaphyseal abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal tapering of metatarsals Gene Set From HPO Gene-Disease Associations genes associated with the distal tapering of metatarsals phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal ileal atresia Gene Set From HPO Gene-Disease Associations genes associated with the distal ileal atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal tapering femur Gene Set From HPO Gene-Disease Associations genes associated with the distal tapering femur phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
ivory epiphyses of the distal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the ivory epiphyses of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of the distal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the duplication of the distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplastic distal humeri Gene Set From HPO Gene-Disease Associations genes associated with the hypoplastic distal humeri phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
complete duplication of the distal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the complete duplication of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
broad distal phalanx of the toes Gene Set From HPO Gene-Disease Associations genes associated with the broad distal phalanx of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal amyotrophy Gene Set From HPO Gene-Disease Associations genes associated with the distal amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
broad distal phalanx of the hallux Gene Set From HPO Gene-Disease Associations genes associated with the broad distal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
wide distal femoral metaphysis Gene Set From HPO Gene-Disease Associations genes associated with the wide distal femoral metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the distal phalanx of the 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the distal phalanx of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal shortening of limbs Gene Set From HPO Gene-Disease Associations genes associated with the distal shortening of limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
osteolytic defects of the distal phalanges of the toes Gene Set From HPO Gene-Disease Associations genes associated with the osteolytic defects of the distal phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal sensory impairment of all modalities Gene Set From HPO Gene-Disease Associations genes associated with the distal sensory impairment of all modalities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
fifth finger distal phalanx clinodactyly Gene Set From HPO Gene-Disease Associations genes associated with the fifth finger distal phalanx clinodactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the distal phalanx of the hallux Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of the distal phalanx of the hallux Gene Set From HPO Gene-Disease Associations genes associated with the duplication of the distal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
club-shaped distal femur Gene Set From HPO Gene-Disease Associations genes associated with the club-shaped distal femur phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short distal phalanx of the 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the short distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the distal phalanges of the toes Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
shortening of all distal phalanges of the fingers Gene Set From HPO Gene-Disease Associations genes associated with the shortening of all distal phalanges of the fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal/middle symphalangism of 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the distal/middle symphalangism of 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the distal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal femoral bowing Gene Set From HPO Gene-Disease Associations genes associated with the distal femoral bowing phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
long distal phalanx of finger Gene Set From HPO Gene-Disease Associations genes associated with the long distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal muscle weakness Gene Set From HPO Gene-Disease Associations genes associated with the distal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absent distal phalanges Gene Set From HPO Gene-Disease Associations genes associated with the absent distal phalanges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal symphalangism Gene Set From HPO Gene-Disease Associations genes associated with the distal symphalangism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized distal tubular acidosis Gene Set From HPO Gene-Disease Associations genes associated with the generalized distal tubular acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short distal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the short distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
partial duplication of the distal phalanx of the hallux Gene Set From HPO Gene-Disease Associations genes associated with the partial duplication of the distal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
bifid distal phalanx of toe Gene Set From HPO Gene-Disease Associations genes associated with the bifid distal phalanx of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypermobility of distal interphalangeal joints Gene Set From HPO Gene-Disease Associations genes associated with the hypermobility of distal interphalangeal joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
irregular distal femoral epiphysis Gene Set From HPO Gene-Disease Associations genes associated with the irregular distal femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short distal phalanx of toe Gene Set From HPO Gene-Disease Associations genes associated with the short distal phalanx of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal renal tubular acidosis Gene Set From HPO Gene-Disease Associations genes associated with the distal renal tubular acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short distal phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the short distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short distal phalanx of the 4th finger Gene Set From HPO Gene-Disease Associations genes associated with the short distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal sensory impairment Gene Set From HPO Gene-Disease Associations genes associated with the distal sensory impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of the distal phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the duplication of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive distal muscle weakness Gene Set From HPO Gene-Disease Associations genes associated with the progressive distal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
tapered distal phalanges of finger Gene Set From HPO Gene-Disease Associations genes associated with the tapered distal phalanges of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal peripheral sensory neuropathy Gene Set From HPO Gene-Disease Associations genes associated with the distal peripheral sensory neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
complete duplication of distal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the complete duplication of distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the distal phalanx of finger Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
acroosteolysis of distal phalanges (feet) Gene Set From HPO Gene-Disease Associations genes associated with the acroosteolysis of distal phalanges (feet) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal tibial bowing Gene Set From HPO Gene-Disease Associations genes associated with the distal tibial bowing phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal urethral duplication Gene Set From HPO Gene-Disease Associations genes associated with the distal urethral duplication phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal sensory loss of all modalities Gene Set From HPO Gene-Disease Associations genes associated with the distal sensory loss of all modalities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
enlargement of the distal femoral epiphysis Gene Set From HPO Gene-Disease Associations genes associated with the enlargement of the distal femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal arthrogryposis Gene Set From HPO Gene-Disease Associations genes associated with the distal arthrogryposis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the distal phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
distal symphalangism (hands) Gene Set From HPO Gene-Disease Associations genes associated with the distal symphalangism (hands) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
impaired distal proprioception Gene Set From HPO Gene-Disease Associations genes associated with the impaired distal proprioception phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absent fourth finger distal interphalangeal crease Gene Set From HPO Gene-Disease Associations genes associated with the absent fourth finger distal interphalangeal crease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Distal-less-like homeobox protein, N-terminal domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Distal-less-like homeobox protein, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
dilated distal convoluted tubules Gene Set From MPO Gene-Phenotype Associations gene mutations causing the dilated distal convoluted tubules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal distal convoluted tubule morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal distal convoluted tubule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal distal visceral endoderm morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal distal visceral endoderm morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal proximal-distal axis patterning Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal proximal-distal axis patterning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent distal visceral endoderm Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent distal visceral endoderm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
neuronopathy, distal hereditary motor, type vi Gene Set From OMIM Gene-Disease Associations genes associated with the neuronopathy, distal hereditary motor, type vi phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, distal, autosomal recessive, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, autosomal recessive, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, distal, autosomal recessive, 5 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, autosomal recessive, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, distal, 4 Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, distal, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
neuronopathy, distal hereditary motor, type vb Gene Set From OMIM Gene-Disease Associations genes associated with the neuronopathy, distal hereditary motor, type vb phenotype from the curated OMIM Gene-Disease Associations dataset.
neuronopathy, distal hereditary motor, type viia Gene Set From OMIM Gene-Disease Associations genes associated with the neuronopathy, distal hereditary motor, type viia phenotype from the curated OMIM Gene-Disease Associations dataset.
arthrogryposis, distal, type 5 Gene Set From OMIM Gene-Disease Associations genes associated with the arthrogryposis, distal, type 5 phenotype from the curated OMIM Gene-Disease Associations dataset.
arthrogryposis, distal, type 3 Gene Set From OMIM Gene-Disease Associations genes associated with the arthrogryposis, distal, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, chronic distal, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, chronic distal, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
neuronopathy, distal hereditary motor, type iid Gene Set From OMIM Gene-Disease Associations genes associated with the neuronopathy, distal hereditary motor, type iid phenotype from the curated OMIM Gene-Disease Associations dataset.
arthyrgryposis, distal, type 2b Gene Set From OMIM Gene-Disease Associations genes associated with the arthyrgryposis, distal, type 2b phenotype from the curated OMIM Gene-Disease Associations dataset.
chromosome 22q11.2 deletion syndrome, distal Gene Set From OMIM Gene-Disease Associations genes associated with the chromosome 22q11.2 deletion syndrome, distal phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, distal hereditary motor, jerash type Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, jerash type phenotype from the curated OMIM Gene-Disease Associations dataset.
arthrogryposis, distal, type 2b Gene Set From OMIM Gene-Disease Associations genes associated with the arthrogryposis, distal, type 2b phenotype from the curated OMIM Gene-Disease Associations dataset.
arthrogryposis, distal, type 2a Gene Set From OMIM Gene-Disease Associations genes associated with the arthrogryposis, distal, type 2a phenotype from the curated OMIM Gene-Disease Associations dataset.
welander distal myopathy Gene Set From OMIM Gene-Disease Associations genes associated with the welander distal myopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
renal tubular acidosis, distal, ar Gene Set From OMIM Gene-Disease Associations genes associated with the renal tubular acidosis, distal, ar phenotype from the curated OMIM Gene-Disease Associations dataset.
renal tubular acidosis, distal, ad Gene Set From OMIM Gene-Disease Associations genes associated with the renal tubular acidosis, distal, ad phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, distal 3 Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, distal 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
laing distal myopathy Gene Set From OMIM Gene-Disease Associations genes associated with the laing distal myopathy phenotype from the curated OMIM Gene-Disease Associations dataset.
?neuronopathy, distal hereditary motor, type iic Gene Set From OMIM Gene-Disease Associations genes associated with the ?neuronopathy, distal hereditary motor, type iic phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, distal hereditary motor, type va Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type va phenotype from the curated OMIM Gene-Disease Associations dataset.
renal tubular acidosis, distal, autosomal recessive Gene Set From OMIM Gene-Disease Associations genes associated with the renal tubular acidosis, distal, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.
arthrogryposis multiplex congenita, distal, type 1 Gene Set From OMIM Gene-Disease Associations genes associated with the arthrogryposis multiplex congenita, distal, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
arthrogryposis multiplex congenita, distal, type 2b Gene Set From OMIM Gene-Disease Associations genes associated with the arthrogryposis multiplex congenita, distal, type 2b phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, distal, with anterior tibial onset Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, distal, with anterior tibial onset phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, distal, x-linked 3 Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, x-linked 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, distal hereditary motor, type viib Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type viib phenotype from the curated OMIM Gene-Disease Associations dataset.
arthrogryposis, distal, type 1b Gene Set From OMIM Gene-Disease Associations genes associated with the arthrogryposis, distal, type 1b phenotype from the curated OMIM Gene-Disease Associations dataset.
spinal muscular atrophy, distal, congenital nonprogressive Gene Set From OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, congenital nonprogressive phenotype from the curated OMIM Gene-Disease Associations dataset.
arthrogryposis, distal, type 5d Gene Set From OMIM Gene-Disease Associations genes associated with the arthrogryposis, distal, type 5d phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, distal, tateyama type Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, distal, tateyama type phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, distal hereditary motor, type iib Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type iib phenotype from the curated OMIM Gene-Disease Associations dataset.
neuropathy, distal hereditary motor, type iia Gene Set From OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type iia phenotype from the curated OMIM Gene-Disease Associations dataset.
distal tip Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue distal tip in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
distal tubular epithelium Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue distal tubular epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
renal distal tubule Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue renal distal tubule in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
distal tip cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue distal tip cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Distal Amyotrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Amyotrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Arthrogryposis Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Arthrogryposis Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Lower Limb Amyotrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Lower Limb Amyotrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Jacobsen Distal 11Q Deletion Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Jacobsen Distal 11Q Deletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Renal Tubular Acidosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Renal Tubular Acidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Distal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Distal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Monosomy 3P Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Monosomy 3P Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Periodic Paralysis With Later-Onset Distal Motor Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Periodic Paralysis With Later-Onset Distal Motor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Broad Distal Phalanges Of All Fingers Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Broad Distal Phalanges Of All Fingers in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 22Q11.2 Deletion Syndrome, Distal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 22Q11.2 Deletion Syndrome, Distal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complete Duplication Of Distal Phalanx Of The Thumb Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complete Duplication Of Distal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Short Distal Phalanx Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Short Distal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Stippling Of The Epiphysis Of The Distal Phalanx Of The Thumb Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Stippling Of The Epiphysis Of The Distal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Fifth Finger Distal Phalanx Clinodactyly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Fifth Finger Distal Phalanx Clinodactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Welander Distal Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Welander Distal Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Upper Limb Amyotrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Upper Limb Amyotrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Ileal Obstruction Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Ileal Obstruction Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Intestinal Obstruction Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Intestinal Obstruction Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Tibial Bowing Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Tibial Bowing in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Irregular Distal Femoral Epiphysis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Irregular Distal Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Flat Distal Femoral Epiphysis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Flat Distal Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Bile Duct Cancer Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Bile Duct Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Aortic Dissection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Aortic Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Tapering Pointed Ends Of Distal Finger Phalanges Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Tapering Pointed Ends Of Distal Finger Phalanges in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Hereditary Motor Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Hereditary Motor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Triangular Shaped Distal Phalanx Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Triangular Shaped Distal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Peripheral Sensory Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Peripheral Sensory Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bifid Distal Phalanx Of Toe Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bifid Distal Phalanx Of Toe in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Arthrogryposis Type 5D Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Arthrogryposis Type 5D in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Monosomy 12P Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Monosomy 12P in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Partial Duplication Of The Distal Phalanx Of The 2Nd Finger Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Partial Duplication Of The Distal Phalanx Of The 2Nd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Partial Duplication Of The Distal Phalanx Of The 3Rd Finger Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Partial Duplication Of The Distal Phalanx Of The 3Rd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Tapering Femur Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Tapering Femur in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Generalized Distal Tubular Acidosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Generalized Distal Tubular Acidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Colitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Colitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Urethral Duplication Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Urethral Duplication in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dysplastic Distal Thumb Phalanges With A Central Hole Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dysplastic Distal Thumb Phalanges With A Central Hole in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Broad Distal Phalanx Of The Hallux Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Broad Distal Phalanx Of The Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Long Distal Phalanx Of Finger Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Long Distal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Klhl9-Related Early-Onset Distal Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Klhl9-Related Early-Onset Distal Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Bile Duct Carcinoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Bile Duct Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complete Duplication Of The Distal Phalanges Of The Hand Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complete Duplication Of The Distal Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acroosteolysis Of Distal Phalanges (Feet) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acroosteolysis Of Distal Phalanges (Feet) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Curved Distal Phalanges Of The Hand Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Curved Distal Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Myopathy 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Myopathy 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Tapering Of Metatarsals Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Tapering Of Metatarsals in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Trisomy 10Q Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Trisomy 10Q Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Absent Fourth Finger Distal Interphalangeal Crease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Absent Fourth Finger Distal Interphalangeal Crease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hyperkalemic Distal Renal Tubular Acidosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hyperkalemic Distal Renal Tubular Acidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal-Type Epithelioid Sarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal-Type Epithelioid Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
B-Cell Immunodeficiency, Distal Limb Anomalies, And Urogenital Malformations Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease B-Cell Immunodeficiency, Distal Limb Anomalies, And Urogenital Malformations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Bullet-Shaped Distal Phalanx Of The Hallux Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Bullet-Shaped Distal Phalanx Of The Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ivory Epiphyses Of The Distal Phalanges Of The Hand Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ivory Epiphyses Of The Distal Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Adult-Onset Distal Myopathy Due To Valosin Containing Protein Mutation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Adult-Onset Distal Myopathy Due To Valosin Containing Protein Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal 17P13.3 Microdeletion Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal 17P13.3 Microdeletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Monosomy 1Q Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Monosomy 1Q in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Monosomy 13Q Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Distal Monosomy 13Q Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chromosome 19Q13.11 Deletion Syndrome, Distal Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 19Q13.11 Deletion Syndrome, Distal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Distal Muscle Weakness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Distal Sensory Impairment Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Sensory Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Distal Phalanx Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Distal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Impaired Distal Proprioception Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Impaired Distal Proprioception in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Distal Muscle Atrophy Due To Neurologic Disease Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Muscle Atrophy Due To Neurologic Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Shortening Of All Distal Phalanges Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Shortening Of All Distal Phalanges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fatigable Weakness Of Distal Limb Muscles Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fatigable Weakness Of Distal Limb Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Late-Onset Distal Muscle Weakness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Late-Onset Distal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Distal Lower Limb Muscle Weakness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Lower Limb Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Distal Upper Limb Muscle Weakness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Upper Limb Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Broad Distal Phalanx Of Finger Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Distal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Club-Shaped Distal Femur Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Club-Shaped Distal Femur in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Distal Sensory Impairment Of All Modalities Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Sensory Impairment Of All Modalities in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Distal Renal Tubular Acidosis Co-Occurrent With Sensorineural Deafness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Renal Tubular Acidosis Co-Occurrent With Sensorineural Deafness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Osteolytic Defects Of The Distal Phalanges Of The Hand Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Osteolytic Defects Of The Distal Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Bifid Distal Phalanx Of The Thumb Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Bifid Distal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Partial Duplication Of The Distal Phalanx Of The Hallux Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Partial Duplication Of The Distal Phalanx Of The Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Impaired Distal Vibration Sensation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Impaired Distal Vibration Sensation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Progressive Distal Muscle Weakness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Distal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Small Distal Femoral Epiphysis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Small Distal Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Wide Tufts Of Distal Phalanges Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Wide Tufts Of Distal Phalanges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hypermobility Of Distal Interphalangeal Joints Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hypermobility Of Distal Interphalangeal Joints in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Distal Joint Laxity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Joint Laxity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of The Distal Phalanx Of The Thumb Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Distal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Impaired Distal Tactile Sensation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Impaired Distal Tactile Sensation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Distal Ileal Atresia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Ileal Atresia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Distal Femoral Bowing Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Femoral Bowing in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Tapered Distal Phalanges Of Finger Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tapered Distal Phalanges Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Duplication Of The Distal Phalanx Of Hand Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Duplication Of The Distal Phalanx Of Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Broad Distal Hallux Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Distal Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Broad Distal Phalanx Of The Thumb Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Distal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Widened Distal Phalanges Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Widened Distal Phalanges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Distal Shortening Of Limbs Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Shortening Of Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absent Distal Interphalangeal Creases Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Distal Interphalangeal Creases in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Enlargement Of The Distal Femoral Epiphysis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Enlargement Of The Distal Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Slender Distal Phalanx Of Finger Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Slender Distal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Distal Acroosteolysis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Acroosteolysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Decreased Distal Sensory Nerve Action Potential Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Distal Sensory Nerve Action Potential in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Distal Ulnar Hypoplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Ulnar Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Distal Widening Of Metacarpals Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Widening Of Metacarpals in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absent Distal Phalanges Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Distal Phalanges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Trapezoidal Distal Femoral Condyles Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Trapezoidal Distal Femoral Condyles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Wide Distal Femoral Metaphysis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Wide Distal Femoral Metaphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Distal/Middle Symphalangism Of 5Th Finger Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal/Middle Symphalangism Of 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
proximal/distal pattern formation Gene Set From GO Biological Process Annotations 2023 genes participating in the proximal/distal pattern formation biological process from the curated GO Biological Process Annotations 2023 dataset.
proximal/distal axis specification Gene Set From GO Biological Process Annotations 2023 genes participating in the proximal/distal axis specification biological process from the curated GO Biological Process Annotations 2023 dataset.
metanephric distal tubule morphogenesis Gene Set From GO Biological Process Annotations 2023 genes participating in the metanephric distal tubule morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.
metanephric distal convoluted tubule development Gene Set From GO Biological Process Annotations 2023 genes participating in the metanephric distal convoluted tubule development biological process from the curated GO Biological Process Annotations 2023 dataset.
metanephric distal tubule development Gene Set From GO Biological Process Annotations 2023 genes participating in the metanephric distal tubule development biological process from the curated GO Biological Process Annotations 2023 dataset.
distal tubule development Gene Set From GO Biological Process Annotations 2023 genes participating in the distal tubule development biological process from the curated GO Biological Process Annotations 2023 dataset.
distal tubule morphogenesis Gene Set From GO Biological Process Annotations 2023 genes participating in the distal tubule morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.
distal convoluted tubule development Gene Set From GO Biological Process Annotations 2023 genes participating in the distal convoluted tubule development biological process from the curated GO Biological Process Annotations 2023 dataset.
distal dendrite Gene Set From GO Cellular Component Annotations 2023 proteins localized to the distal dendrite cellular component from the curated GO Cellular Component Annotations 2023 dataset.
apical distal dendrite Gene Set From GO Cellular Component Annotations 2023 proteins localized to the apical distal dendrite cellular component from the curated GO Cellular Component Annotations 2023 dataset.
dilated distal convoluted tubule Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the dilated distal convoluted tubule phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal distal convoluted tubule morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal distal convoluted tubule morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal proximal-distal axis patterning Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal proximal-distal axis patterning phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal distal visceral endoderm morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal distal visceral endoderm morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent distal visceral endoderm Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent distal visceral endoderm phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased distal limb length Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased distal limb length phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Human - Kidney - L1 - Distal Convoluted Tubule Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L1 - Distal Convoluted Tubule cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Kidney - L2 - Distal Convoluted Tubule Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Distal Convoluted Tubule cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Kidney - L3 - Distal Convoluted Tubule Type 1 Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Distal Convoluted Tubule Type 1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Kidney - L3 - Distal Convoluted Tubule Type 2 Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Distal Convoluted Tubule Type 2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Distal epithelial cell_Distal airway_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Distal epithelial cell_Distal airway_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Distal Proliferative Progenitor cell_Bone_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Distal Proliferative Progenitor cell_Bone_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Distal limb bud cell_Limb bud_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Distal limb bud cell_Limb bud_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Enterocyte distal cell_Intestine_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Enterocyte distal cell_Intestine_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Distal cell_Epithelium_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Distal cell_Epithelium_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Distal stem cell_Epithelium_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Distal stem cell_Epithelium_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Distal convoluted tubular cell_Kidney_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Distal convoluted tubular cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Distal tubule & loop of Henle cell_Fetal kidney_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Distal tubule & loop of Henle cell_Fetal kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Distal tubular cell_Fetal kidney_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Distal tubular cell_Fetal kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Medial and distal segment cell_Fetal kidney_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Medial and distal segment cell_Fetal kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Distal tubular cell_Kidney_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Distal tubular cell_Kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Distal tubular cell_Kidney_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Distal tubular cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Distal convoluted tubular cell_Kidney_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Distal convoluted tubular cell_Kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Distal cell_Blood vessel_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Distal cell_Blood vessel_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Distal lung progenitor cell_Lung_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Distal lung progenitor cell_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Distal epithelial cell_Lung_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Distal epithelial cell_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Distal cell_Prostate_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Distal cell_Prostate_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Distal convoluted tubular cell_Epithelium_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Distal convoluted tubular cell_Epithelium_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
16p11 2 distal deletion syndrome Gene Set From WikiPathways Pathways 2024 proteins participating in the 16p11 2 distal deletion syndrome pathway from the WikiPathways Pathways 2024 dataset.
Defective SLC4A1 causes hereditary spherocytosis type 4 (HSP4), distal renal tubular acidosis (dRTA) and dRTA with hemolytic anemia (dRTA-HA) Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC4A1 causes hereditary spherocytosis type 4 (HSP4), distal renal tubular acidosis (dRTA) and dRTA with hemolytic anemia (dRTA-HA) pathway from the Reactome Pathways 2024 dataset.
Defective SLC5A7 causes distal hereditary motor neuronopathy 7A (HMN7A)_5619114 Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC5A7 causes distal hereditary motor neuronopathy 7A (HMN7A)_5619114 pathway from the Reactome Pathways 2024 dataset.
Defective SLC5A7 causes distal hereditary motor neuronopathy 7A (HMN7A)_5658471 Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC5A7 causes distal hereditary motor neuronopathy 7A (HMN7A)_5658471 pathway from the Reactome Pathways 2024 dataset.
proximal/distal pattern formation Gene Set From GO Biological Process Annotations 2025 genes participating in the proximal/distal pattern formation biological process from the curated GO Biological Process Annotations 2025 dataset.
proximal/distal axis specification Gene Set From GO Biological Process Annotations 2025 genes participating in the proximal/distal axis specification biological process from the curated GO Biological Process Annotations 2025 dataset.
metanephric distal tubule morphogenesis Gene Set From GO Biological Process Annotations 2025 genes participating in the metanephric distal tubule morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.
metanephric distal convoluted tubule development Gene Set From GO Biological Process Annotations 2025 genes participating in the metanephric distal convoluted tubule development biological process from the curated GO Biological Process Annotations 2025 dataset.
metanephric distal tubule development Gene Set From GO Biological Process Annotations 2025 genes participating in the metanephric distal tubule development biological process from the curated GO Biological Process Annotations 2025 dataset.
distal tubule development Gene Set From GO Biological Process Annotations 2025 genes participating in the distal tubule development biological process from the curated GO Biological Process Annotations 2025 dataset.
distal tubule morphogenesis Gene Set From GO Biological Process Annotations 2025 genes participating in the distal tubule morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.
distal convoluted tubule development Gene Set From GO Biological Process Annotations 2025 genes participating in the distal convoluted tubule development biological process from the curated GO Biological Process Annotations 2025 dataset.
distal dendrite Gene Set From GO Cellular Component Annotations 2025 proteins localized to the distal dendrite cellular component from the curated GO Cellular Component Annotations 2025 dataset.
apical distal dendrite Gene Set From GO Cellular Component Annotations 2025 proteins localized to the apical distal dendrite cellular component from the curated GO Cellular Component Annotations 2025 dataset.
Distal arthrogryposis Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal arthrogryposis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant distal hereditary motor neuronopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant distal hereditary motor neuronopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant distal hereditary motor neuronopathy 5 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant distal hereditary motor neuronopathy 5 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Distal arthrogryposis type 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal arthrogryposis type 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Distal myopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal recessive distal hereditary motor neuronopathy 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal recessive distal hereditary motor neuronopathy 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal recessive distal hereditary motor neuronopathy Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal recessive distal hereditary motor neuronopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Distal arthrogryposis type 2B Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal arthrogryposis type 2B from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Distal 10q deletion syndrome Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal 10q deletion syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Distal myopathy 1 Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal myopathy 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Distal arthrogryposis type 5D Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 5D in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis type 2A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 2A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal myopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant distal hereditary motor neuronopathy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant distal hereditary motor neuronopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant distal hereditary motor neuronopathy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal myopathy with rimmed vacuoles Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy with rimmed vacuoles in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis type 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant distal hereditary motor neuronopathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal myopathy with anterior tibial onset Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy with anterior tibial onset in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis type 2B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 2B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal myopathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive distal hereditary motor neuronopathy 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive distal hereditary motor neuronopathy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive distal hereditary motor neuronopathy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant distal hereditary motor neuronopathy 14 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chromosome 22q11.2 deletion syndrome, distal Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 22q11.2 deletion syndrome, distal in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant distal hereditary motor neuronopathy 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal myopathy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant distal hereditary motor neuronopathy 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked distal spinal muscular atrophy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked distal spinal muscular atrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive distal hereditary motor neuronopathy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis type 1B Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 1B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis type 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis type 1A Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 1A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant distal hereditary motor neuronopathy 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant distal hereditary motor neuronopathy 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant distal hereditary motor neuronopathy 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant distal hereditary motor neuronopathy 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis type 1C Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 1C in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis type 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Partial trisomy distal 4q Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Partial trisomy distal 4q in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis type 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal 10q deletion syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal 10q deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal myopathy 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive distal hereditary motor neuronopathy 5 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis type 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive distal hereditary motor neuronopathy 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis type 6 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive distal hereditary motor neuronopathy 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis type 2B2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 2B2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis type 2B1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 2B1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Distal arthrogryposis type 2B3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 2B3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Renal distal tubule Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Renal distal tubule in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Distal tip cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Distal tip cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Distal tip Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Distal tip in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Distal tubular epithelium Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Distal tubular epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Distal axon Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Distal axon cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Distal portion of axoneme Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Distal portion of axoneme cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Distal dendrite Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Distal dendrite cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Apical distal dendrite Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Apical distal dendrite cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Photoreceptor distal connecting cilium Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Photoreceptor distal connecting cilium cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Distal axon Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Distal axon cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Distal dendrite Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Distal dendrite cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Photoreceptor distal connecting cilium Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Photoreceptor distal connecting cilium cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Distal portion of axoneme Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Distal portion of axoneme cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Basal distal dendrite Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Basal distal dendrite cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Apical distal dendrite Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Apical distal dendrite cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
bacterial-type flagellum basal body, distal rod, L ring Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the bacterial-type flagellum basal body, distal rod, L ring cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
bacterial-type flagellum basal body, distal rod Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the bacterial-type flagellum basal body, distal rod cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Distal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive distal renal tubular acidosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive distal renal tubular acidosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive distal muscle weakness Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive distal muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Distal myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive distal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive distal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked distal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked distal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Distal renal tubular acidosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal renal tubular acidosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Distal arthrogryposis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal arthrogryposis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Distal muscle weakness Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Distal lower limb muscle weakness Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal lower limb muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Distal lower limb amyotrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal lower limb amyotrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Distal hereditary motor neuropathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal hereditary motor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant distal renal tubular acidosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant distal renal tubular acidosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive scapulohumeroperoneal distal myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive scapulohumeroperoneal distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Arthrogryposis multiplex congenita distal Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Arthrogryposis multiplex congenita distal phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Welander distal myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Welander distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Distal shortening of limbs Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal shortening of limbs phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Finnish upper limb-onset distal myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Finnish upper limb-onset distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Distal/Left-sided colorectal cancer Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Distal/Left-sided colorectal cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Distal colorectal cancer Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Distal colorectal cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
PMC8104016-hcg-12-e002353-s006.xlsx-mTHP-1-LPS_Prom-Distal-RefSeq_Name_IRF6 Gene Set From Rummagene Transcription Factor Associations 2026 target genes of the PMC8104016-hcg-12-e002353-s006.xlsx-mTHP-1-LPS_Prom-Distal-RefSeq_Name_IRF6 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.
increased number of circulating vldl and idl particles Gene Set From GAD Gene-Disease Associations genes associated with the disease increased number of circulating vldl and idl particles in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
number Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term number in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
maintenance of cell number Gene Set From GO Biological Process Annotations 2015 genes participating in the maintenance of cell number biological process from the curated GO Biological Process Annotations 2015 dataset.
homeostasis of number of cells Gene Set From GO Biological Process Annotations 2015 genes participating in the homeostasis of number of cells biological process from the curated GO Biological Process Annotations 2015 dataset.
homeostasis of number of cells in a free-living population Gene Set From GO Biological Process Annotations 2015 genes participating in the homeostasis of number of cells in a free-living population biological process from the curated GO Biological Process Annotations 2015 dataset.
homeostasis of number of cells within a tissue Gene Set From GO Biological Process Annotations 2015 genes participating in the homeostasis of number of cells within a tissue biological process from the curated GO Biological Process Annotations 2015 dataset.
Primary tooth development (number of teeth) Gene Set From 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.
abnormal neutrophil cell number Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormal neutrophil cell number phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormal number of teeth Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormal number of teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
reduced number of teeth Gene Set From GWASdb SNP-Phenotype Associations genes associated with the reduced number of teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormal number of vertebrae Gene Set From HPO Gene-Disease Associations genes associated with the abnormal number of vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased number of sweat glands Gene Set From HPO Gene-Disease Associations genes associated with the decreased number of sweat glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
increased number of teeth Gene Set From HPO Gene-Disease Associations genes associated with the increased number of teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
reduced number of intrahepatic bile ducts Gene Set From HPO Gene-Disease Associations genes associated with the reduced number of intrahepatic bile ducts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased number of cd8+ t cells Gene Set From HPO Gene-Disease Associations genes associated with the decreased number of cd8+ t cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of b cell number Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of b cell number phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased number of small peripheral myelinated nerve fibers Gene Set From HPO Gene-Disease Associations genes associated with the decreased number of small peripheral myelinated nerve fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased number of large peripheral myelinated nerve fibers Gene Set From HPO Gene-Disease Associations genes associated with the decreased number of large peripheral myelinated nerve fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal number of incisors Gene Set From HPO Gene-Disease Associations genes associated with the abnormal number of incisors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
increased number of cd4-/cd8- t cells expressing alpha/beta t-cell receptors Gene Set From HPO Gene-Disease Associations genes associated with the increased number of cd4-/cd8- t cells expressing alpha/beta t-cell receptors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased number of cd4+ t cells Gene Set From HPO Gene-Disease Associations genes associated with the decreased number of cd4+ t cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
increased number of peripheral cd3+ t cells Gene Set From HPO Gene-Disease Associations genes associated with the increased number of peripheral cd3+ t cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
reduced number of corneal endothelial cells Gene Set From HPO Gene-Disease Associations genes associated with the reduced number of corneal endothelial cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal number of permanent teeth Gene Set From HPO Gene-Disease Associations genes associated with the abnormal number of permanent teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
increase in t cell number Gene Set From HPO Gene-Disease Associations genes associated with the increase in t cell number phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal number of teeth Gene Set From HPO Gene-Disease Associations genes associated with the abnormal number of teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased number of peripheral myelinated nerve fibers Gene Set From HPO Gene-Disease Associations genes associated with the decreased number of peripheral myelinated nerve fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of t cell number Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of t cell number phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal neutrophil cell number Gene Set From HPO Gene-Disease Associations genes associated with the abnormal neutrophil cell number phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal number of erythroid precursors Gene Set From HPO Gene-Disease Associations genes associated with the abnormal number of erythroid precursors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
increase in b cell number Gene Set From HPO Gene-Disease Associations genes associated with the increase in b cell number phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
reduced number of teeth Gene Set From HPO Gene-Disease Associations genes associated with the reduced number of teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
fatty acid β-oxidation (unsaturated, odd number) Gene Set From HumanCyc Pathways proteins participating in the fatty acid β-oxidation (unsaturated, odd number) pathway from the HumanCyc Pathways dataset.
abnormal fetal derived definitive erythrocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal derived definitive erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal bone marrow cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal bone marrow cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased white fat cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased white fat cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased brown fat cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased brown fat cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased nk cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased nk cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased osteoclast cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased osteoclast cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased oocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased oocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased enteric neural crest cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased enteric neural crest cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal primordial ovarian follicle number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal primordial ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cochlear inner hair cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear inner hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased eosinophil cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased eosinophil cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal purkinje cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal purkinje cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cd4-positive, cd25-positive, alpha-beta regulatory t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cd4-positive, cd25-positive, alpha-beta regulatory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased dendritic cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased dendritic cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased glomerular capillary number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased glomerular capillary number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased pre-pro b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased pre-pro b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased t-helper 17 cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased t-helper 17 cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal plasmacytoid dendritic cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal plasmacytoid dendritic cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased memory t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal memory t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cochlear hair cell stereocilia number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cochlear hair cell stereocilia number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased number of peritubular myoid cells Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased number of peritubular myoid cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased bone marrow cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased bone marrow cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased transitional stage t2 b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased transitional stage t2 b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased trophoblast glycogen cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased trophoblast glycogen cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased eosinophil cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased eosinophil cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased gonadotroph cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased gonadotroph cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased sebaceous gland number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased sebaceous gland number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal plasma cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal plasma cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased neuron number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased neuron number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased secondary ovarian follicle number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased secondary ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased plasma cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased plasma cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased respiratory mucosa goblet cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased respiratory mucosa goblet cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal neuron number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal neuron number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased lumbar vertebrae number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased lumbar vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased number of pulmonary neuroendocrine bodies Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased number of pulmonary neuroendocrine bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased sacral vertebrae number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased sacral vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal lymphocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal lymphocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased platelet cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased platelet cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cd8-positive, alpha-beta t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cd8-positive, alpha-beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased oligodendrocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased oligodendrocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased pancreatic islet number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased pancreatic islet number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal nk t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal nk t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased lymph node number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased lymph node number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased organ of corti supporting cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased organ of corti supporting cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased keratohyalin granule number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased keratohyalin granule number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal mast cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal mast cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased t-helper 17 cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased t-helper 17 cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased amacrine cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased amacrine cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased hemangioblast number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased hemangioblast number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased hepatoblast number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased hepatoblast number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased oligodendrocyte progenitor number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased oligodendrocyte progenitor number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased chondrocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased chondrocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased hippocampus pyramidal cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased hippocampus pyramidal cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased b-1 b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased b-1 b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased t-helper 2 cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased t-helper 2 cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased prostate gland duct number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased prostate gland duct number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased salivary gland mucosal cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased salivary gland mucosal cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased thymocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased thymocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased activated t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased activated t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased skeletal muscle fiber number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased skeletal muscle fiber number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased otolith number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased otolith number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased vestibular hair cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased vestibular hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased nk t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased nk t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased double-negative t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased double-negative t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased primordial ovarian follicle number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased primordial ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased common myeloid progenitor cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased common myeloid progenitor cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal hemangioblast number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal hemangioblast number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased retinal cone cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased retinal cone cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased corpora lutea number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased corpora lutea number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased mitochondria number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased mitochondria number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cochlear hair cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cochlear hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased pp cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased pp cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased regulatory t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased regulatory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased lumbar vertebrae number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased lumbar vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased b-1b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased b-1b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased germ cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased germ cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased pancreatic beta cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased pancreatic beta cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cajal-retzius cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cajal-retzius cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased transitional stage t1 b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased transitional stage t1 b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased pancreatic islet number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased pancreatic islet number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal primary ovarian follicle number Gene Set From 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 peyer's patch number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal peyer's patch number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal organ of corti supporting cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal organ of corti supporting cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cerebellar granule cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cerebellar granule cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased cochlear inner hair cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased cochlear inner hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased alveolar lamellar body number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased alveolar lamellar body number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal reticulocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal reticulocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased single-positive t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased single-positive t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased rib number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased rib number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased kidney collecting duct number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased kidney collecting duct number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased retinal ganglion cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased retinal ganglion cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased macrophage cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased macrophage cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cd4-positive, cd25-positive, alpha-beta regulatory t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cd4-positive, cd25-positive, alpha-beta regulatory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased sebocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased sebocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased sebaceous gland number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased sebaceous gland number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased neutrophil cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased neutrophil cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased erythroblast number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased erythroblast number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased ly6c low monocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased ly6c low monocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased vertebrae number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased lactotroph cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased lactotroph cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal amacrine cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal amacrine cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased myocardial fiber number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased myocardial fiber number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal brown fat cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal brown fat cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal b-1 b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal b-1 b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal osteoclast cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal osteoclast cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased endometrial gland number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased endometrial gland number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased immature b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased immature b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased mitochondria number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased mitochondria number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased late pro-b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased late pro-b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal myeloid dendritic cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal myeloid dendritic cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal sternebra number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal sternebra number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased cd4-positive, alpha-beta memory t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased cd4-positive, alpha-beta memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased cochlear outer hair cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased cochlear outer hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased t-helper 2 cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased t-helper 2 cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased pancreatic delta cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased pancreatic delta cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased molar number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased molar number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased dn1 thymic pro-t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased dn1 thymic pro-t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased metatarsal bone number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased metatarsal bone number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal lymph node number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal lymph node number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased plasma cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased plasma cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal klrg1-positive nk cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal klrg1-positive nk cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased vascular endothelial cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased vascular endothelial cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased dn1 thymic pro-t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased dn1 thymic pro-t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased pp cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased pp cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased type ii pneumocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased type ii pneumocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased b-1a cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased b-1a cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased pancreatic epsilon cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased pancreatic epsilon cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased satellite cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased satellite cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased gamma-delta t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased gamma-delta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased thyrotroph cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased thyrotroph cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased hair follicle number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased hair follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal white fat cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal white fat cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased mature b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased mature b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased splenocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased splenocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased leukocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased leukocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased pancreatic alpha cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased pancreatic alpha cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased basophil cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased basophil cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased immature b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased immature b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal t follicular helper cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal t follicular helper cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased splenocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased splenocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased macrophage cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased macrophage cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased pancreatic acinar cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased pancreatic acinar cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased transitional stage b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased transitional stage b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased retinal photoreceptor cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased retinal photoreceptor cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal leukocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal leukocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased transitional stage b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased transitional stage b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased marginal zone b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased marginal zone b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased erythroid progenitor cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased erythroid progenitor cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased mature ovarian follicle number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased mature ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased sebocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased sebocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased primordial germ cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased primordial germ cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased transitional stage t2 b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased transitional stage t2 b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased monocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased monocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal brown fat lipid droplet number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal brown fat lipid droplet number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal synaptic vesicle number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal synaptic vesicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased megakaryocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased megakaryocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased retinal photoreceptor cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased retinal photoreceptor cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal vestibular hair cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal vestibular hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased hematopoietic stem cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased hematopoietic stem cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased secondary ovarian follicle number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased secondary ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased thoracic vertebrae number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased thoracic vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased caudal vertebrae number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased caudal vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cd4-positive, alpha-beta memory t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cd4-positive, alpha-beta memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal nk cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal nk cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased memory b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased memory b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased osteoclast cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased osteoclast cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased hepatocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased hepatocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased presacral vertebrae number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased presacral vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased granulocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased granulocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal effector memory cd4-positive, alpha-beta t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal effector memory cd4-positive, alpha-beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal monocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal monocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased somatotroph secretory granule number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased somatotroph secretory granule number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal t-helper 2 cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal t-helper 2 cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased lymph node number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased lymph node number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased klrg1+ cd4 alpha beta t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased klrg1+ cd4 alpha beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased t helper 1 cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased t helper 1 cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased vascular endothelial cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased vascular endothelial cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased transitional stage t1 b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased transitional stage t1 b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal chromosome number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal chromosome number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased bronchioalveolar stem cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased bronchioalveolar stem cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased clara cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased clara cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased alpha-beta t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased alpha-beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased nucleated erythrocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased nucleated erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased number of howell-jolly bodies Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased number of howell-jolly bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal alpha-beta t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal alpha-beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased lactotroph cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased lactotroph cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased amacrine cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased amacrine cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal ly6c low monocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal ly6c low monocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased monocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased monocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased hematopoietic stem cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased hematopoietic stem cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased muscle spindle number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased muscle spindle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased purkinje cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased purkinje cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cd8-positive, alpha-beta t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cd8-positive, alpha-beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased primary ovarian follicle number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased primary ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased lymphatic vessel endothelial cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased lymphatic vessel endothelial cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased corpora lutea number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased corpora lutea number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased dopaminergic neuron number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased dopaminergic neuron number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased pancreatic delta cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased pancreatic delta cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased regulatory t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased regulatory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased osteoblast cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased osteoblast cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased b-2 b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased b-2 b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased pro-b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased pro-b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased organ of corti supporting cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased organ of corti supporting cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal skin cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal skin cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased effector memory cd8-positive, alpha-beta t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased effector memory cd8-positive, alpha-beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased myeloid dendritic cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased myeloid dendritic cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased motor neuron number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased motor neuron number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased uterine nk cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased uterine nk cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased mast cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased mast cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal klrg1+ cd4 alpha beta t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal klrg1+ cd4 alpha beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased thymocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased thymocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased platelet cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased platelet cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased gonadotroph cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased gonadotroph cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased granulocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased granulocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal vertebrae number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased purkinje cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased purkinje cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased memory t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal platelet dense granule number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal platelet dense granule number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased mature b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased mature b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased basophil cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased basophil cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal memory b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal memory b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal sperm number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal sperm number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased enterocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased enterocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased pre-b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased pre-b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased thecal cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased thecal cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased sternebra number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased sternebra number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal osteoblast cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal osteoblast cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased tracheal cartilage ring number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased tracheal cartilage ring number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal thecal cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal thecal cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased b-1 b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased b-1 b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased nk t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased nk t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased mature ovarian follicle number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased mature ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
low mean erythrocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the low mean erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased macrophage derived foam cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased macrophage derived foam cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased pre-b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased pre-b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased megakaryocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased megakaryocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased skeletal muscle fiber number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased skeletal muscle fiber number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal endometrial gland number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal endometrial gland number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal secondary ovarian follicle number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal secondary ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased respiratory mucosa goblet cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased respiratory mucosa goblet cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased germinal center b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased germinal center b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased double-positive t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased double-positive t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased klrg1-positive nk cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased klrg1-positive nk cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cerebral cortex pyramidal cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cerebral cortex pyramidal cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal enterocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal enterocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased plasmacytoid dendritic cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased plasmacytoid dendritic cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased embryonic cilium number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased embryonic cilium number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased spleen germinal center number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased spleen germinal center number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased rib number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased rib number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased neuronal precursor cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased neuronal precursor cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased effector memory cd4-positive, alpha-beta t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased effector memory cd4-positive, alpha-beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased leukocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased leukocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal erythroblast number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal erythroblast number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
high mean erythrocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the high mean erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cranial neural crest cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cranial neural crest cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cochlear inner hair cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cochlear inner hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased caudal vertebrae number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased caudal vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased plasmacytoid dendritic cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased plasmacytoid dendritic cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased transitional stage t3 b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased transitional stage t3 b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal basophil cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal basophil cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased germinal center b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased germinal center b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased erythrocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased outer hair cell stereocilia number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased outer hair cell stereocilia number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased retinal ganglion cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased retinal ganglion cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal intraepithelial t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal intraepithelial t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased follicular dendritic cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased follicular dendritic cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal klrg1+ cd8 alpha beta t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal klrg1+ cd8 alpha beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased mature gamma-delta t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased mature gamma-delta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cd4-positive, alpha beta t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cd4-positive, alpha beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased pre-pro b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased pre-pro b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased inner hair cell stereocilia number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased inner hair cell stereocilia number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased oligodendrocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased oligodendrocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased hippocampus pyramidal cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased hippocampus pyramidal cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cd4-positive, alpha beta t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cd4-positive, alpha beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal platelet cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal platelet cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal nucleated erythrocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal nucleated erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased deiters cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased deiters cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased melanocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased melanocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased naive b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased naive b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased fetal derived definitive erythrocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased fetal derived definitive erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased dn2 thymocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased dn2 thymocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased activated t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased activated t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased bone marrow cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased bone marrow cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased neutrophil cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased neutrophil cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased brown fat lipid droplet number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased brown fat lipid droplet number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased presacral vertebrae number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased presacral vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased double-negative t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased double-negative t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased thyrotroph cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased thyrotroph cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased lymphocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased lymphocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased retinal rod cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased retinal rod cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal melanocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal melanocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased hematopoietic cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased hematopoietic cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased neuron number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased neuron number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased somatotroph cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased somatotroph cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
reduced hair shaft melanin granule number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the reduced hair shaft melanin granule number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal pancreatic islet number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreatic islet number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased t follicular helper cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased t follicular helper cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased oligodendrocyte progenitor number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased oligodendrocyte progenitor number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal gamma-delta t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal gamma-delta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cd8-positive, alpha-beta memory t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cd8-positive, alpha-beta memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased clara cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased clara cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cd8-positive, gamma-delta intraepithelial t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cd8-positive, gamma-delta intraepithelial t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased pancreatic epsilon cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased pancreatic epsilon cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased alveolar lamellar body number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased alveolar lamellar body number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal nephron number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal nephron number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased satellite cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased satellite cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal ovarian follicle number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased erythroblast number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased erythroblast number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal eosinophil cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal eosinophil cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased b-1a cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased b-1a cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased renal glomerulus number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased renal glomerulus number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased hematopoietic cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased hematopoietic cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased dendritic cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased dendritic cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased spleen germinal center number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased spleen germinal center number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased muscle spindle number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased muscle spindle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased sensory neuron number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased sensory neuron number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased thecal cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased thecal cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased nephron number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased nephron number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased endometrial gland number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased endometrial gland number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased sternebra number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased sternebra number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased erythroid progenitor cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased erythroid progenitor cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased peyer's patch number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased peyer's patch number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased uterine nk cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased uterine nk cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased brown fat cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased brown fat cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal ly6c high monocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal ly6c high monocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased gamma-delta intraepithelial t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased gamma-delta intraepithelial t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cochlear outer hair cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear outer hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased cochlear hair cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased cochlear hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased trophoblast giant cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased trophoblast giant cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased schwann cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased schwann cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased osteoblast cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased osteoblast cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal t-helper 17 cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal t-helper 17 cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased motor neuron number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased motor neuron number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased somite number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased somite number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased number of pulmonary neuroendocrine bodies Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased number of pulmonary neuroendocrine bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cd4-positive, alpha-beta memory t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cd4-positive, alpha-beta memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased corticotroph cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased corticotroph cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal splenocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal splenocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased mature gamma-delta t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased mature gamma-delta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased metacarpal bone number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased metacarpal bone number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased solitary pulmonary neuroendocrine cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased solitary pulmonary neuroendocrine cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased pancreatic beta cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased pancreatic beta cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal langerhans cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal langerhans cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal oocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal oocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cochlear outer hair cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cochlear outer hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal neutrophil cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal neutrophil cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased cd8-positive, alpha-beta t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased cd8-positive, alpha-beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased single-positive t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased single-positive t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal single-positive t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal single-positive t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased white fat cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased white fat cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cardiac neural crest cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cardiac neural crest cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal vibrissa number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal vibrissa number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased respiratory motile cilia number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased respiratory motile cilia number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cervical vertebrae number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cervical vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased lymphocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased lymphocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased spinal cord ventral horn cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased spinal cord ventral horn cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal sebocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal sebocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased type i pneumocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased type i pneumocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased marginal zone b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased marginal zone b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased transitional stage t3 b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased transitional stage t3 b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased sensory neuron number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased sensory neuron number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased pancreatic alpha cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased pancreatic alpha cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal t-helper 1 cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal t-helper 1 cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased thoracic vertebrae number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased thoracic vertebrae number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased pancreatic acinar cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased pancreatic acinar cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased retinal cone cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased retinal cone cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased male germ cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased male germ cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal respiratory motile cilium number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal respiratory motile cilium number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased schwann cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased schwann cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased nk cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased nk cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased dn4 thymocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased dn4 thymocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased erythrocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cd8-positive, alpha-beta memory t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cd8-positive, alpha-beta memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased dn3 thymocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased dn3 thymocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal regulatory t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal regulatory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased pro-b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased pro-b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal granulocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal granulocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal effector memory cd8-positive, alpha-beta t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal effector memory cd8-positive, alpha-beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased t-helper 1 cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased t-helper 1 cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased langerhans cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased langerhans cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased astrocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased astrocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased myeloid dendritic cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased myeloid dendritic cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased trophoblast giant cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased trophoblast giant cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased vestibular hair cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased vestibular hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased mast cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased mast cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased alpha-beta t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased alpha-beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased gamma-delta t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased gamma-delta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal sebaceous gland number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal sebaceous gland number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased number of heinz bodies Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased number of heinz bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased follicular b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased follicular b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal hematopoietic cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal hematopoietic cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased enterocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased enterocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased cd4-positive, cd25-positive, alpha-beta regulatory t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased cd4-positive, cd25-positive, alpha-beta regulatory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased neural crest cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased neural crest cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased solitary pulmonary neuroendocrine cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased solitary pulmonary neuroendocrine cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased vestibular hair cell stereocilia number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased vestibular hair cell stereocilia number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased bone trabecula number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased bone trabecula number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased myocardial fiber number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased myocardial fiber number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal erythrocyte cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased b-2 b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased b-2 b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal astrocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal astrocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal neuronal precursor cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal neuronal precursor cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased podocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased podocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased b-1b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased b-1b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased cd8-positive, alpha-beta memory t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased cd8-positive, alpha-beta memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal kidney collecting duct number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney collecting duct number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased gamma-delta intraepithelial t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased gamma-delta intraepithelial t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal macrophage cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal macrophage cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased double-positive t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased double-positive t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased ly6c high monocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased ly6c high monocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased bone trabecula number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased bone trabecula number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased follicular b cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased follicular b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased trophoblast glycogen cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased trophoblast glycogen cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased dn2 thymocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased dn2 thymocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased cd4-positive, alpha beta t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased cd4-positive, alpha beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased peyer's patch number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased peyer's patch number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased dn3 thymocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased dn3 thymocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased klrg1+ cd8 alpha beta t cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased klrg1+ cd8 alpha beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased t follicular helper cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased t follicular helper cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased schwann cell precursor number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased schwann cell precursor number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal dendritic cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal dendritic cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
increased neuronal precursor cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the increased neuronal precursor cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased type ii pneumocyte number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased type ii pneumocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Harmonizome 3.0

7q11 23 distal copy number variation Gene Set

7q11 23 copy number variation syndrome Gene Set

22q11 2 copy number variation syndrome Gene Set

1q21 1 copy number variation syndrome Gene Set

3q29 copy number variation syndrome Gene Set

15q11 2 copy number variation syndrome Gene Set

15q13 3 copy number variation syndrome Gene Set

2q11 2 copy number variation syndrome Gene Set

2q13 copy number variation syndrome Gene Set

2q21 1 copy number variation syndrome Gene Set

2q37 copy number variation syndrome Gene Set

17q12 copy number variation syndrome Gene Set

1p36 copy number variation syndrome Gene Set

8p23 1 copy number variation syndrome Gene Set

11p11 2 copy number variation syndrome Gene Set

10q11 21q11 23 copy number variation syndrome Gene Set

4p16 3 copy number variation Gene Set

NF1 copy number variation syndrome Gene Set

17p13 3 YWHAE copy number variation Gene Set

5q35 copy number variation Gene Set

Smith Magenis and Potocki Lupski syndrome copy number variation Gene Set

6q16 copy number variation Gene Set

10q22q23 copy number variation Gene Set

13q12 or CRYL1 copy number variation Gene Set

13q12 12 copy number variation Gene Set

15q11q13 copy number variation Gene Set

15q25 copy number variation Gene Set

PAFAH1B1 copy number variation Gene Set

8q11 23 RB1CC1 copy number variation Gene Set

chromosome 7q11.23 deletion syndrome, distal, 1.2mb Gene Set

Mitochondrial DNA copy number (white blood cells) Gene Set

Mitochondrial DNA copy number Gene Set

Epstein-Barr virus copy number in lymphoblastoid cell lines Gene Set

chromosome 7q11.23 duplication syndrome Gene Set

7q11.23 duplication syndrome Gene Set

7q11.23 duplication syndrome Gene Set

copy Gene Set

Impdh2 enzyme activity, variation in Gene Set

Skin/hair/eye pigmentation, variation in, 1 Gene Set

Skin/hair/eye pigmentation, variation in, 8 Gene Set

Skin/hair/eye pigmentation, variation in, 4 Gene Set

Skin/hair/eye pigmentation, variation in, 5 Gene Set

Skin/hair/eye pigmentation, variation in, 9 Gene Set

Skin/hair/eye pigmentation, variation in, 10 Gene Set

Skin/hair/eye pigmentation, variation in, 11 Gene Set

Apocrine gland secretion, variation in Gene Set

QT INTERVAL, VARIATION IN Gene Set

quantitative variation in lipid and lipoprotein traits Gene Set

normmal variation Gene Set

normal variation in leptin levels Gene Set

nomal variation Gene Set

pharmacogenetic variation Gene Set

dyslexia; reading; normal variation Gene Set

variation in platelet integrin alpha 2 beta 1 density Gene Set

variation in plasma lipoproteins Gene Set

quantitative variation in plasma high-density lipoproteins and triacylglycerides Gene Set

normal variation Gene Set

variation Gene Set

DNA methylation (variation) Gene Set

patchy variation in bone mineral density Gene Set

[skin/hair/eye pigmentation, variation in, 8] Gene Set

[axillary odor, variation in] Gene Set

[colostrum secretion, variation in] Gene Set

[skin/hair/eye pigmentation, variation in, 11 (melanesian blond hair)] Gene Set

[qt interval, variation in] Gene Set

{gene expression, variation in, qtl} Gene Set

[impdh2 enzyme activity, variation in] Gene Set

[bone mineral density variation qtl] Gene Set

{obesity, variation in} Gene Set

Impdh2 Enzyme Activity, Variation In Gene Set

Patchy Variation In Bone Mineral Density Gene Set

Myopathy caused by variation in F Gene Set

Myopathy caused by variation in POMG Gene Set

Myopathy caused by variation in PO Gene Set

DNA methylation (variation) Gene Set

Distal hereditary motor neuronopathy 2D Gene Set

Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss Gene Set

Renal tubular acidosis, distal, autosomal dominant Gene Set

Renal tubular acidosis, distal, autosomal recessive Gene Set