| Name |
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SMNDC1 Genesurvival motor neuron domain containing 1 This gene is a paralog of SMN1 gene, which encodes the survival motor neuron protein, mutations in which are cause of autosomal recessive proximal spinal muscular atrophy. The protein encoded by this gene is a nuclear protein that has been identified as a constituent of the spliceosome complex. This gene is differentially expressed, with abundant levels in skeletal muscle, and may share similar cellular function as the SMN1 gene. [provided by RefSeq, Jul 2008] |
MNX1 Genemotor neuron and pancreas homeobox 1 This gene encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009] |
SMN2 Genesurvival of motor neuron 2, centromeric This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. The telomeric and centromeric copies of this gene are nearly identical and encode the same protein. While mutations in the telomeric copy are associated with spinal muscular atrophy, mutations in this gene, the centromeric copy, do not lead to disease. This gene may be a modifier of disease caused by mutation in the telomeric copy. The critical sequence difference between the two genes is a single nucleotide in exon 7, which is thought to be an exon splice enhancer. Note that the nine exons of both the telomeric and centromeric copies are designated historically as exon 1, 2a, 2b, and 3-8. It is thought that gene conversion events may involve the two genes, leading to varying copy numbers of each gene. The full length protein encoded by this gene localizes to both the cytoplasm and the nucleus. Within the nucleus, the protein localizes to subnuclear bodies called gems which are found near coiled bodies containing high concentrations of small ribonucleoproteins (snRNPs). This protein forms heteromeric complexes with proteins such as SIP1 and GEMIN4, and also interacts with several proteins known to be involved in the biogenesis of snRNPs, such as hnRNP U protein and the small nucleolar RNA binding protein. Four transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Sep 2008] |
SMN1 Genesurvival of motor neuron 1, telomeric This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. The telomeric and centromeric copies of this gene are nearly identical and encode the same protein. However, mutations in this gene, the telomeric copy, are associated with spinal muscular atrophy; mutations in the centromeric copy do not lead to disease. The centromeric copy may be a modifier of disease caused by mutation in the telomeric copy. The critical sequence difference between the two genes is a single nucleotide in exon 7, which is thought to be an exon splice enhancer. Note that the nine exons of both the telomeric and centromeric copies are designated historically as exon 1, 2a, 2b, and 3-8. It is thought that gene conversion events may involve the two genes, leading to varying copy numbers of each gene. The protein encoded by this gene localizes to both the cytoplasm and the nucleus. Within the nucleus, the protein localizes to subnuclear bodies called gems which are found near coiled bodies containing high concentrations of small ribonucleoproteins (snRNPs). This protein forms heteromeric complexes with proteins such as SIP1 and GEMIN4, and also interacts with several proteins known to be involved in the biogenesis of snRNPs, such as hnRNP U protein and the small nucleolar RNA binding protein. Multiple transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2014] |
SMNP Genesurvival of motor neuron 1, telomeric pseudogene |
LOC100132090 Genesurvival of motor neuron 1, telomeric pseudogene |
EMWX Geneepisodic muscle weakness, X-linked |
UCMA Geneupper zone of growth plate and cartilage matrix associated This gene encodes a chondrocyte-specific, highly charged protein that is abundantly expressed in the upper immature zone of fetal and juvenile epiphyseal cartilage. The encoded protein undergoes proteolytic processing to generate a mature protein that is secreted into the extracellular matrix. The glutamic acid residues in the encoded protein undergo gamma carboxylation in a vitamin K-dependent manner. Undercarboxylation of the encoded protein is associated with osteoarthritis in humans. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2015] |
OPHLC GeneOmphalocele due to duplication of 1p31.3 |
PSHK2 GenePseudohyperkalemia, familial, 2, due to red cell leak |
SM2 GeneHepatic fibrosis susceptibility due to Schistosoma mansoni infection |
SMAN1 Genesurvival of motor and autonomic neurons 1 |
HMN7A GeneMotor neuronopathy, distal hereditary, type VIIA |
HMSN5 GeneHereditary motor and sensory neuropathy V |
NMSR GeneNeuropathy, hereditary motor and sensory, Russe type |
PAM16 Genepresequence translocase-associated motor 16 homolog (S. cerevisiae) This gene encodes a mitochondrial protein involved in granulocyte-macrophage colony-stimulating factor (GM-CSF) signaling. This protein also plays a role in the import of nuclear-encoded mitochondrial proteins into the mitochondrial matrix and may be important in reactive oxygen species (ROS) homeostasis. Mutations in this gene cause Megarbane-Dagher-Melike type spondylometaphyseal dysplasia, an early lethal skeletal dysplasia characterized by short stature, developmental delay and other skeletal abnormalities. [provided by RefSeq, May 2017] |
HMNJ GeneDistal hereditary motor neuropathy, Jerash type |
HMSNO GeneNeuropathy, hereditary motor and sensory, Okinawa type |
CALY Genecalcyon neuron-specific vesicular protein The protein encoded by this gene is a type II single transmembrane protein. It is required for maximal stimulated calcium release after stimulation of purinergic or muscarinic but not beta-adrenergic receptors. The encoded protein interacts with D1 dopamine receptor and may interact with other DA receptor subtypes and/or GPCRs. [provided by RefSeq, Jul 2008] |
NDNF Geneneuron-derived neurotrophic factor Predicted to enable heparin binding activity. Involved in several processes, including cellular response to hypoxia; negative regulation of apoptotic process; and nitric oxide mediated signal transduction. Located in extracellular region. Is active in extracellular space. Implicated in hypogonadotropic hypogonadism. [provided by Alliance of Genome Resources, Mar 2025] |
NAV3 Geneneuron navigator 3 This gene belongs to the neuron navigator family and is expressed predominantly in the nervous system. The encoded protein contains coiled-coil domains and a conserved AAA domain characteristic for ATPases associated with a variety of cellular activities. This gene is similar to unc-53, a Caenorhabditis elegans gene involved in axon guidance. Multiple alternatively spliced transcript variants for this gene have been described but only one has had its full-length nature determined. [provided by RefSeq, Jul 2008] |
NAV2 Geneneuron navigator 2 This gene encodes a member of the neuron navigator gene family, which may play a role in cellular growth and migration. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011] |
NSG1 Geneneuron specific gene family member 1 Predicted to enable clathrin light chain binding activity. Involved in apoptotic process. Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025] |
ELAVL4 GeneELAV like neuron-specific RNA binding protein 4 Enables mRNA 3'-UTR AU-rich region binding activity; poly(A) binding activity; and pre-mRNA intronic pyrimidine-rich binding activity. Involved in 3'-UTR-mediated mRNA stabilization; RNA processing; and positive regulation of 3'-UTR-mediated mRNA stabilization. Predicted to be located in axon; cytoplasm; and dendrite. Predicted to be part of ribonucleoprotein complex. Predicted to be active in glutamatergic synapse. [provided by Alliance of Genome Resources, Mar 2025] |
ELAVL2 GeneELAV like neuron-specific RNA binding protein 2 In humans, the ELAV like RNA binding protein gene family has four members (ELAVL1-4). ELAVL RNA binding proteins recognize AU-rich elements in the 3' UTRs of gene transcripts and thereby regulate gene expression post-transcriptionally. The protein encoded by this gene binds to several 3' UTRs, including its own and also that of FOS, ID, and POU5F1. This gene encodes ELAVL2 and, like ELAVL3 and ELAVL4, is expressed specifically in neurons and primarily localizes to the cytoplasm. This protein also forms a cytosolic complex with the normally nuclear-localized ELAVL1 protein. Alternative splicing of this gene results in multiple transcript variants encoding distinct protein isoforms. [provided by RefSeq, Jul 2020] |
ELAVL3 GeneELAV like neuron-specific RNA binding protein 3 A member of the ELAVL protein family, ELAV-like 3 is a neural-specific RNA-binding protein which contains three RNP-type RNA recognition motifs. The observation that ELAVL3 is one of several Hu antigens (neuronal-specific RNA-binding proteins) recognized by the anti-Hu serum antibody present in sera from patients with paraneoplastic encephalomyelitis and sensory neuronopathy (PEM/PSN) suggests it has a role in neurogenesis. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
NAV1 Geneneuron navigator 1 This gene belongs to the neuron navigator family and is expressed predominantly in the nervous system. The encoded protein contains coiled-coil domains and a conserved AAA domain characteristic for ATPases associated with a variety of cellular activities. This gene is similar to unc-53, a Caenorhabditis elegans gene involved in axon guidance. The exact function of this gene is not known, but it is thought to play a role in in neuronal development and regeneration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2009] |
weakness due to upper motor neuron dysfunction Gene SetFrom HPO Gene-Disease Associations genes associated with the weakness due to upper motor neuron dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Weakness Due To Upper Motor Neuron Dysfunction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Weakness Due To Upper Motor Neuron Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
upper motor neuron dysfunction Gene SetFrom HPO Gene-Disease Associations genes associated with the upper motor neuron dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Upper Motor Neuron Dysfunction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Motor Neuron Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
abnormal upper motor neuron morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal upper motor neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Abnormal Upper Motor Neuron Morphology Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Upper Motor Neuron Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Upper Motor Neuron Signs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Motor Neuron Signs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
distal upper limb muscle weakness Gene SetFrom 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. |
upper limb muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the upper limb muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal muscle weakness in upper limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal muscle weakness in upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Distal Upper Limb Muscle Weakness Gene SetFrom 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. |
Proximal Muscle Weakness In Upper Limbs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Muscle Weakness In Upper Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
myocardial infarction; ventricular dysfunction, left; ventricular dysfunction, right Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial infarction; ventricular dysfunction, left; ventricular dysfunction, right in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
respiratory insufficiency due to muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the respiratory insufficiency due to muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
intermittent episodes of respiratory insufficiency due to muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the intermittent episodes of respiratory insufficiency due to muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Respiratory Insufficiency Due To Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Respiratory Insufficiency Due To Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Intermittent Episodes Of Respiratory Insufficiency Due To Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intermittent Episodes Of Respiratory Insufficiency Due To Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Immune dysfunction with T-cell inactivation due to calcium entry defect 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Immune dysfunction with T-cell inactivation due to calcium entry defect 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Immune dysfunction with T-cell inactivation due to calcium entry defect 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Immune dysfunction with T-cell inactivation due to calcium entry defect 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Immune dysfunction with T-cell inactivation due to calcium entry defect 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Immune dysfunction with T-cell inactivation due to calcium entry defect 1 from the curated CTD Gene-Disease Associations dataset. |
Immune dysfunction with T-cell inactivation due to calcium entry defect 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Immune dysfunction with T-cell inactivation due to calcium entry defect 2 from the curated CTD Gene-Disease Associations dataset. |
decreased sweating due to autonomic dysfunction Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased sweating due to autonomic dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
orthostatic hypotension due to autonomic dysfunction Gene SetFrom HPO Gene-Disease Associations genes associated with the orthostatic hypotension due to autonomic dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Orthostatic Hypotension Due To Autonomic Dysfunction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Orthostatic Hypotension Due To Autonomic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Sweating Due To Autonomic Dysfunction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Sweating Due To Autonomic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease THROMBOPHILIA, FAMILIAL, DUE TO DECREASED RELEASE OF TISSUE PLASMINOGEN ACTIVATOR;THPH9 HYPERFIBRINOLYSIS, FAMILIAL, DUE TO INCREASED RELEASE OF TISSUE PLASMINOGEN from the curated CTD Gene-Disease Associations dataset. |
charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy Gene SetFrom GAD Gene-Disease Associations genes associated with the disease charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Primary motor cortex cell_Primary motor cortex_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Primary motor cortex cell_Primary motor cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Motor Neuron Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Motor Neuron Disease from the curated CTD Gene-Disease Associations dataset. |
motor neuron disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease motor neuron disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
motor neuron disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease motor neuron disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
motor neuron disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease motor neuron disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
survival motor neuron spinal muscular atrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease survival motor neuron spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
sporadic adult-onset lower motor neuron disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sporadic adult-onset lower motor neuron disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
motor neuron disease; paraparesis, spastic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease motor neuron disease; paraparesis, spastic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
motor neuron disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease motor neuron disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bulbar-onset motor neuron disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bulbar-onset motor neuron disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aphasia; dementia; motor neuron disease; neurodegenerative diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aphasia; dementia; motor neuron disease; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
smoothened signaling pathway involved in spinal cord motor neuron cell fate specification Gene SetFrom GO Biological Process Annotations 2015 genes participating in the smoothened signaling pathway involved in spinal cord motor neuron cell fate specification biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of motor neuron apoptotic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of motor neuron apoptotic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
motor neuron apoptotic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the motor neuron apoptotic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of lateral motor column neuron migration Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of lateral motor column neuron migration biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of transcription from rna polymerase ii promoter involved in spinal cord motor neuron fate specification Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of transcription from rna polymerase ii promoter involved in spinal cord motor neuron fate specification biological process from the curated GO Biological Process Annotations 2015 dataset. |
somatic motor neuron differentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the somatic motor neuron differentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
medial motor column neuron differentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the medial motor column neuron differentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
lateral motor column neuron migration Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lateral motor column neuron migration biological process from the curated GO Biological Process Annotations 2015 dataset. |
fasciculation of motor neuron axon Gene SetFrom GO Biological Process Annotations 2015 genes participating in the fasciculation of motor neuron axon biological process from the curated GO Biological Process Annotations 2015 dataset. |
motor neuron axon guidance Gene SetFrom GO Biological Process Annotations 2015 genes participating in the motor neuron axon guidance biological process from the curated GO Biological Process Annotations 2015 dataset. |
spinal cord motor neuron cell fate specification Gene SetFrom GO Biological Process Annotations 2015 genes participating in the spinal cord motor neuron cell fate specification biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of transcription from rna polymerase ii promoter involved in somatic motor neuron fate commitment Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of transcription from rna polymerase ii promoter involved in somatic motor neuron fate commitment biological process from the curated GO Biological Process Annotations 2015 dataset. |
visceral motor neuron differentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the visceral motor neuron differentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
motor neuron migration Gene SetFrom GO Biological Process Annotations 2015 genes participating in the motor neuron migration biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of motor neuron apoptotic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of motor neuron apoptotic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of lateral motor column neuron migration Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of lateral motor column neuron migration biological process from the curated GO Biological Process Annotations 2015 dataset. |
spinal cord motor neuron migration Gene SetFrom GO Biological Process Annotations 2015 genes participating in the spinal cord motor neuron migration biological process from the curated GO Biological Process Annotations 2015 dataset. |
spinal cord motor neuron differentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the spinal cord motor neuron differentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
motor neuron disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease motor neuron disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
abnormal motor neuron morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal motor neuron morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
motor neuron atrophy Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the motor neuron atrophy phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
motor neuron atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the motor neuron atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal lower motor neuron morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal lower motor neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal motor neuron morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal motor neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Motor Neuron Disease Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Motor Neuron Disease phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Survival motor neuron Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Survival motor neuron protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
decreased motor neuron number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased motor neuron number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
motor neuron degeneration Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the motor neuron degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased motor neuron number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased motor neuron number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal motor neuron innervation pattern Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal motor neuron innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal motor neuron morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal motor neuron morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Motor Neuron Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Motor Neuron Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Motor Neuron Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Motor Neuron Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Familial Motor Neuron Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Familial Motor Neuron Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Frontotemporal Dementia With Motor Neuron Disease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Frontotemporal Dementia With Motor Neuron Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Autosomal Recessive Lower Motor Neuron Disease With Childhood Onset Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Lower Motor Neuron Disease With Childhood Onset in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormal Motor Neuron Morphology Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Motor Neuron Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormal Lower Motor Neuron Morphology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Lower Motor Neuron Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
motor neuron migration Gene SetFrom GO Biological Process Annotations 2023 genes participating in the motor neuron migration biological process from the curated GO Biological Process Annotations 2023 dataset. |
motor neuron axon guidance Gene SetFrom GO Biological Process Annotations 2023 genes participating in the motor neuron axon guidance biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of motor neuron apoptotic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of motor neuron apoptotic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
fasciculation of motor neuron axon Gene SetFrom GO Biological Process Annotations 2023 genes participating in the fasciculation of motor neuron axon biological process from the curated GO Biological Process Annotations 2023 dataset. |
lateral motor column neuron migration Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lateral motor column neuron migration biological process from the curated GO Biological Process Annotations 2023 dataset. |
spinal cord motor neuron differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the spinal cord motor neuron differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of motor neuron apoptotic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of motor neuron apoptotic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
visceral motor neuron differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the visceral motor neuron differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
spinal cord motor neuron cell fate specification Gene SetFrom GO Biological Process Annotations 2023 genes participating in the spinal cord motor neuron cell fate specification biological process from the curated GO Biological Process Annotations 2023 dataset. |
motor neuron apoptotic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the motor neuron apoptotic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
spinal cord motor neuron migration Gene SetFrom GO Biological Process Annotations 2023 genes participating in the spinal cord motor neuron migration biological process from the curated GO Biological Process Annotations 2023 dataset. |
abnormal motor neuron morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal motor neuron morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased motor neuron number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased motor neuron number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased motor neuron number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased motor neuron number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal motor neuron innervation pattern Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal motor neuron innervation pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
motor neuron degeneration Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the motor neuron degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal motor neuron dendrite morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal motor neuron dendrite morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Human - Motor Cortex - Class - Glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Class - Glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Class - GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Class - GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Subclass - Layer 2-3 glutamatergic neuron, intratelencephalon-projecting Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - Layer 2-3 glutamatergic neuron, intratelencephalon-projecting cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Subclass - Layer 5 glutamatergic neuron, extratelencephalon-projecting Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - Layer 5 glutamatergic neuron, extratelencephalon-projecting cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Subclass - Layer 5 glutamatergic neuron, intratelencephalon-projecting Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - Layer 5 glutamatergic neuron, intratelencephalon-projecting cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Subclass - Layer 5-6 glutamatergic neuron, near-projecting Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - Layer 5-6 glutamatergic neuron, near-projecting cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Subclass - Layer 6 glutamatergic neuron, corticothalamic-projecting Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - Layer 6 glutamatergic neuron, corticothalamic-projecting cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Subclass - Layer 6 glutamatergic neuron, intratelencephalon-projecting Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - Layer 6 glutamatergic neuron, intratelencephalon-projecting cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Subclass - Layer 6 Car3+ glutamatergic neuron, intratelencephalon-projecting Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - Layer 6 Car3+ glutamatergic neuron, intratelencephalon-projecting cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Subclass - Layer 6b glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - Layer 6b glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Subclass - Lamp5+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - Lamp5+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Subclass - Pvalb+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - Pvalb+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Subclass - Sncg+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - Sncg+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Subclass - Sst+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - Sst+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Subclass - Sst+ Chodl+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - Sst+ Chodl+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Subclass - Vip+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Subclass - Vip+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - LAMP5+ KCNG3+ Layer 2 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - LAMP5+ KCNG3+ Layer 2 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - LINC00507+ ATP7B+ Layer 2 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - LINC00507+ ATP7B+ Layer 2 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - LINC00507+ GLRA3+ Layer 2 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - LINC00507+ GLRA3+ Layer 2 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - LINC00507+ DSG3+ Layer 2-3 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - LINC00507+ DSG3+ Layer 2-3 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - RORB+ CCDC68+ Layer 2-3 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - RORB+ CCDC68+ Layer 2-3 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - RORB+ PTPN3+ Layer 2-3 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - RORB+ PTPN3+ Layer 2-3 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - RORB+ RTKN2+ Layer 2-3 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - RORB+ RTKN2+ Layer 2-3 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - LAMP5+ CARM1P1+ Layer 3 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - LAMP5+ CARM1P1+ Layer 3 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - RORB+ OTOGL+ Layer 3 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - RORB+ OTOGL+ Layer 3 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - THEMIS+ ENPEP+ Layer 3 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - THEMIS+ ENPEP+ Layer 3 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - FEZF2+ ASGR2+ Layer 3-5 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ ASGR2+ Layer 3-5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - FEZF2+ LINC01107+ Layer 3-5 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ LINC01107+ Layer 3-5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - RORB+ LAMA4+ Layer 3-5 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - RORB+ LAMA4+ Layer 3-5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - RORB+ LINC01202+ Layer 3-5 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - RORB+ LINC01202+ Layer 3-5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - RORB+ LNX2+ Layer 3-5 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - RORB+ LNX2+ Layer 3-5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - RORB+ RPRM+ Layer 3-5 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - RORB+ RPRM+ Layer 3-5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - RORB+ TNNT2+ Layer 3-5 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - RORB+ TNNT2+ Layer 3-5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - FEZF2+ CSN1S1+ Layer 5 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ CSN1S1+ Layer 5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - FEZF2+ NREP-AS1+ Layer 5 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ NREP-AS1+ Layer 5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - FEZF2+ PKD2L1+ Layer 5 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ PKD2L1+ Layer 5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - FEZF2+ RNF144A-AS1+ Layer 5 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ RNF144A-AS1+ Layer 5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - RORB+ MED8+ Layer 5 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - RORB+ MED8+ Layer 5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - THEMIS+ FGF10+ Layer 5 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - THEMIS+ FGF10+ Layer 5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - THEMIS+ LINC01116+ Layer 5 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - THEMIS+ LINC01116+ Layer 5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - THEMIS+ RGPD6+ Layer 5 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - THEMIS+ RGPD6+ Layer 5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - THEMIS+ SLC22A18+ Layer 5 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - THEMIS+ SLC22A18+ Layer 5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - THEMIS+ VILL+ Layer 5 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - THEMIS+ VILL+ Layer 5 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - FEZF2+ C9orf135-AS1+ Layer 5-6 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ C9orf135-AS1+ Layer 5-6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - FEZF2+ CFTR+ Layer 5-6 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ CFTR+ Layer 5-6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - FEZF2+ FILIP1L+ Layer 5-6 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ FILIP1L+ Layer 5-6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - FEZF2+ IFNG-AS1+ Layer 5-6 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ IFNG-AS1+ Layer 5-6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - FEZF2+ LPO+ Layer 5-6 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ LPO+ Layer 5-6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - FEZF2+ OR1L8+ Layer 5-6 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ OR1L8+ Layer 5-6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - FEZF2+ SH2D1B+ Layer 5-6 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ SH2D1B+ Layer 5-6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - THEMIS+ SMYD1+ Layer 5-6 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - THEMIS+ SMYD1+ Layer 5-6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - THEMIS+ TNFAIP6+ Layer 5-6 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - THEMIS+ TNFAIP6+ Layer 5-6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - FEZF2+ FFAR4+ Layer 6 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ FFAR4+ Layer 6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - FEZF2+ KLK7+ Layer 6 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ KLK7+ Layer 6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - FEZF2+ PDYN+ Layer 6 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ PDYN+ Layer 6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - FEZF2+ POGK+ Layer 6 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ POGK+ Layer 6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - FEZF2+ PROKR2+ Layer 6 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - FEZF2+ PROKR2+ Layer 6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - THEMIS+ LINC00343+ Layer 6 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - THEMIS+ LINC00343+ Layer 6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - THEMIS+ SLN+ Layer 6 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - THEMIS+ SLN+ Layer 6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - THEMIS+ SNTG2+ Layer 6 glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - THEMIS+ SNTG2+ Layer 6 glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - LAMP5+ BMP2+ Layer 1 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - LAMP5+ BMP2+ Layer 1 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - LAMP5+ NMBR+ Layer 1 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - LAMP5+ NMBR+ Layer 1 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - LAMP5+ PVRL2+ Layer 1 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - LAMP5+ PVRL2+ Layer 1 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - LAMP5+ RAB11FIP1+ Layer 1 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - LAMP5+ RAB11FIP1+ Layer 1 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - PAX6+ CHRFAM7A+ Layer 1 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PAX6+ CHRFAM7A+ Layer 1 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - PAX6+ MIR101-1+ Layer 1 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PAX6+ MIR101-1+ Layer 1 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - PVALB+ SST ASIC4+ Layer 1 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PVALB+ SST ASIC4+ Layer 1 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - SST+ DEFB108B+ Layer 1 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ DEFB108B+ Layer 1 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - SST+ P4HA3+ Layer 1 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ P4HA3+ Layer 1 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - VIP+ KLHDC8B+ Layer 1 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ KLHDC8B+ Layer 1 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - PVALB+ CDK20+ Layer 1-2 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PVALB+ CDK20+ Layer 1-2 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - SST+ CCNJL+ Layer 1-2 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ CCNJL+ Layer 1-2 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - SST+ CLIC6+ Layer 1-2 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ CLIC6+ Layer 1-2 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - SST+ PRRT4+ Layer 1-2 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ PRRT4+ Layer 1-2 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - VIP+ EXPH5+ Layer 1-2 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ EXPH5+ Layer 1-2 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - VIP+ HTR3A+ Layer 1-2 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ HTR3A+ Layer 1-2 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - VIP+ PTGER3+ Layer 1-2 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ PTGER3+ Layer 1-2 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - VIP+ SCML4+ Layer 1-2 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ SCML4+ Layer 1-2 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - VIP+ WNT4+ Layer 1-2 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ WNT4+ Layer 1-2 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - SST+ FAM20A+ Layer 1-3 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ FAM20A+ Layer 1-3 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - VIP+ CBLN1+ Layer 1-3 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ CBLN1+ Layer 1-3 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - VIP+ CHRNA2+ Layer 1-3 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ CHRNA2+ Layer 1-3 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - VIP+ FNDC1+ Layer 1-3 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ FNDC1+ Layer 1-3 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - VIP+ HSPB6+ Layer 1-3 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ HSPB6+ Layer 1-3 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - VIP+ CD27-AS1+ Layer 1-5 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ CD27-AS1+ Layer 1-5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - VIP+ LINC01013+ Layer 1-5 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ LINC01013+ Layer 1-5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - VIP+ PHLDB3+ Layer 1-5 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ PHLDB3+ Layer 1-5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - VIP+ SMOC1+ Layer 1-5 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ SMOC1+ Layer 1-5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - LAMP5+ AARD+ Layer 1-6 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - LAMP5+ AARD+ Layer 1-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - LAMP5+ CA1+ Layer 1-6 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - LAMP5+ CA1+ Layer 1-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - LAMP5+ NES+ Layer 1-6 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - LAMP5+ NES+ Layer 1-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - PVALB+ COL15A1+ Layer 1-6 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PVALB+ COL15A1+ Layer 1-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - SST+ NPY+ Layer 1-6 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ NPY+ Layer 1-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - VIP+ SLC7A6OS+ Layer 1-6 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ SLC7A6OS+ Layer 1-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - PAX6+ FREM2+ Layer 2 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PAX6+ FREM2+ Layer 2 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - PVALB+ FRZB+ Layer 2 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PVALB+ FRZB+ Layer 2 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - VIP+ SLC6A16+ Layer 2 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ SLC6A16+ Layer 2 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - SST+ NMU+ Layer 2-3 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ NMU+ Layer 2-3 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - PVALB+ HHIPL1+ Layer 2-5 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PVALB+ HHIPL1+ Layer 2-5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - PVALB+ RPH3AL+ Layer 2-5 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PVALB+ RPH3AL+ Layer 2-5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - VIP+ BSPRY+ Layer 2-5 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ BSPRY+ Layer 2-5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - VIP+ SOX11+ Layer 2-5 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ SOX11+ Layer 2-5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - PVALB+ SAMD13+ Layer 3 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PVALB+ SAMD13+ Layer 3 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - PVALB+ ISG20+ Layer 3-5 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PVALB+ ISG20+ Layer 3-5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - SST+ CDH3+ Layer 3-5 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ CDH3+ Layer 3-5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - SST+ GGTLC3+ Layer 3-5 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ GGTLC3+ Layer 3-5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - SST+ OR5AH1P+ Layer 3-5 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ OR5AH1P+ Layer 3-5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - VIP+ HS3ST3A1+ Layer 3-5 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ HS3ST3A1+ Layer 3-5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - VIP+ IGDCC3+ Layer 3-5 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ IGDCC3+ Layer 3-5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - VIP+ TAC3+ Layer 3-5 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ TAC3+ Layer 3-5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - PAX6+ LINC01497+ Layer 3-6 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PAX6+ LINC01497+ Layer 3-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - VIP+ UG0898H09+ Layer 3-6 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ UG0898H09+ Layer 3-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - VIP+ ZIM2-AS1+ Layer 3-6 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ ZIM2-AS1+ Layer 3-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - PVALB+ LRIG3+ Layer 5 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PVALB+ LRIG3+ Layer 5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - SST+ RPL35AP11+ Layer 5 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ RPL35AP11+ Layer 5 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - LAMP5+ CRABP1+ Layer 5-6 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - LAMP5+ CRABP1+ Layer 5-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - PVALB+ FAM150B+ Layer 5-6 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PVALB+ FAM150B+ Layer 5-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - PVALB+ GAPDHP60+ Layer 5-6 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PVALB+ GAPDHP60+ Layer 5-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - PVALB+ KCNIP2+ Layer 5-6 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PVALB+ KCNIP2+ Layer 5-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - PVALB+ MEPE+ Layer 5-6 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PVALB+ MEPE+ Layer 5-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - PVALB+ SST CRHR2+ Layer 5-6 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PVALB+ SST CRHR2+ Layer 5-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - PVALB+ ZFPM2-AS1+ Layer 5-6 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - PVALB+ ZFPM2-AS1+ Layer 5-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - SST+ BEAN1+ Layer 5-6 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ BEAN1+ Layer 5-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - SST+ C4orf26+ Layer 5-6 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ C4orf26+ Layer 5-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - SST+ DNAJC14+ Layer 5-6 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ DNAJC14+ Layer 5-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - SST+ FBN2+ Layer 5-6 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ FBN2+ Layer 5-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - SST+ ISX+ Layer 5-6 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ ISX+ Layer 5-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - SST+ KLHL1+ Layer 5-6 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ KLHL1+ Layer 5-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - SST+ PAWR+ Layer 5-6 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ PAWR+ Layer 5-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - SST+ PIK3CD+ Layer 5-6 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ PIK3CD+ Layer 5-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - VIP+ COL4A3+ Layer 5-6 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - VIP+ COL4A3+ Layer 5-6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cluster - SST+ TH+ Layer 6 GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cluster - SST+ TH+ Layer 6 GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cross-Species Cluster - Chandelier neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cross-Species Cluster - Chandelier neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cross-Species Cluster - Layer 2-3 glutamatergic neuron, intratelencephalon-projecting Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cross-Species Cluster - Layer 2-3 glutamatergic neuron, intratelencephalon-projecting cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cross-Species Cluster - Layer 5 glutamatergic neuron, extratelencephalon-projecting_1 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cross-Species Cluster - Layer 5 glutamatergic neuron, extratelencephalon-projecting_1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cross-Species Cluster - Layer 5 glutamatergic neuron, extratelencephalon-projecting_2 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cross-Species Cluster - Layer 5 glutamatergic neuron, extratelencephalon-projecting_2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cross-Species Cluster - Layer 5 glutamatergic neuron, intratelencephalon-projecting_1 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cross-Species Cluster - Layer 5 glutamatergic neuron, intratelencephalon-projecting_1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cross-Species Cluster - Layer 5 glutamatergic neuron, intratelencephalon-projecting_2 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cross-Species Cluster - Layer 5 glutamatergic neuron, intratelencephalon-projecting_2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cross-Species Cluster - Layer 5 glutamatergic neuron, intratelencephalon-projecting_3 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cross-Species Cluster - Layer 5 glutamatergic neuron, intratelencephalon-projecting_3 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cross-Species Cluster - Layer 5-6 glutamatergic neuron, near-projecting Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cross-Species Cluster - Layer 5-6 glutamatergic neuron, near-projecting cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cross-Species Cluster - Layer 6 glutamatergic neuron, corticothalamic-projecting_1 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cross-Species Cluster - Layer 6 glutamatergic neuron, corticothalamic-projecting_1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cross-Species Cluster - Layer 6 glutamatergic neuron, corticothalamic-projecting_2 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cross-Species Cluster - Layer 6 glutamatergic neuron, corticothalamic-projecting_2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cross-Species Cluster - Layer 6 glutamatergic neuron, intratelencephalon-projecting_1 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cross-Species Cluster - Layer 6 glutamatergic neuron, intratelencephalon-projecting_1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cross-Species Cluster - Layer 6 glutamatergic neuron, intratelencephalon-projecting_2 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cross-Species Cluster - Layer 6 glutamatergic neuron, intratelencephalon-projecting_2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cross-Species Cluster - Layer 6 glutamatergic neuron, intratelencephalon-projecting_3 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cross-Species Cluster - Layer 6 glutamatergic neuron, intratelencephalon-projecting_3 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cross-Species Cluster - Layer 6b glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cross-Species Cluster - Layer 6b glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Motor Cortex - Cross-Species Cluster - Sst+ Chodl+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Motor Cortex - Cross-Species Cluster - Sst+ Chodl+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Class - Glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Class - Glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Class - GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Class - GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Subclass - Layer 2-3 glutamatergic neuron, intratelencephalon-projecting Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Subclass - Layer 2-3 glutamatergic neuron, intratelencephalon-projecting cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Subclass - Layer 5 glutamatergic neuron, extratelencephalon-projecting Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Subclass - Layer 5 glutamatergic neuron, extratelencephalon-projecting cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Subclass - Layer 5 glutamatergic neuron, intratelencephalon-projecting Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Subclass - Layer 5 glutamatergic neuron, intratelencephalon-projecting cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Subclass - Layer 5-6 glutamatergic neuron, near-projecting Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Subclass - Layer 5-6 glutamatergic neuron, near-projecting cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Subclass - Layer 6 glutamatergic neuron, corticothalamic-projecting Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Subclass - Layer 6 glutamatergic neuron, corticothalamic-projecting cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Subclass - Layer 6 glutamatergic neuron, intratelencephalon-projecting Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Subclass - Layer 6 glutamatergic neuron, intratelencephalon-projecting cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Subclass - Layer 6 Car3+ glutamatergic neuron, intratelencephalon-projecting Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Subclass - Layer 6 Car3+ glutamatergic neuron, intratelencephalon-projecting cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Subclass - Layer 6b glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Subclass - Layer 6b glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Subclass - Lamp5+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Subclass - Lamp5+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Subclass - Meis2+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Subclass - Meis2+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Subclass - Pvalb+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Subclass - Pvalb+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Subclass - Sncg+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Subclass - Sncg+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Subclass - Sst+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Subclass - Sst+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Subclass - Sst+ Chodl+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Subclass - Sst+ Chodl+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Subclass - Vip+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Subclass - Vip+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Layer 2-3 glutamatergic neuron, intratelencephalon-projecting_1 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Layer 2-3 glutamatergic neuron, intratelencephalon-projecting_1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Layer 2-3 glutamatergic neuron, intratelencephalon-projecting_2 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Layer 2-3 glutamatergic neuron, intratelencephalon-projecting_2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Layer 2-3 glutamatergic neuron, intratelencephalon-projecting_3 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Layer 2-3 glutamatergic neuron, intratelencephalon-projecting_3 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Layer 5 glutamatergic neuron, extratelencephalon-projecting_1 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Layer 5 glutamatergic neuron, extratelencephalon-projecting_1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Layer 5 glutamatergic neuron, extratelencephalon-projecting_2 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Layer 5 glutamatergic neuron, extratelencephalon-projecting_2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Layer 5 glutamatergic neuron, extratelencephalon-projecting_3 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Layer 5 glutamatergic neuron, extratelencephalon-projecting_3 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Layer 5 glutamatergic neuron, extratelencephalon-projecting_4 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Layer 5 glutamatergic neuron, extratelencephalon-projecting_4 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Pld5+ Layer 5 glutamatergic neuron, intratelencephalon-projecting_1 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Pld5+ Layer 5 glutamatergic neuron, intratelencephalon-projecting_1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Pld5+ Layer 5 glutamatergic neuron, intratelencephalon-projecting_2 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Pld5+ Layer 5 glutamatergic neuron, intratelencephalon-projecting_2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Rspo1+ Layer 5 glutamatergic neuron, intratelencephalon-projecting_1 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Rspo1+ Layer 5 glutamatergic neuron, intratelencephalon-projecting_1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Rspo1+ Layer 5 glutamatergic neuron, intratelencephalon-projecting_2 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Rspo1+ Layer 5 glutamatergic neuron, intratelencephalon-projecting_2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - S100b+ Layer 5 glutamatergic neuron, intratelencephalon-projecting_1 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - S100b+ Layer 5 glutamatergic neuron, intratelencephalon-projecting_1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - S100b+ Layer 5 glutamatergic neuron, intratelencephalon-projecting_2 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - S100b+ Layer 5 glutamatergic neuron, intratelencephalon-projecting_2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Layer 5-6 glutamatergic neuron, near-projecting_CT Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Layer 5-6 glutamatergic neuron, near-projecting_CT cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Layer 5-6 glutamatergic neuron, near-projecting_1 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Layer 5-6 glutamatergic neuron, near-projecting_1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Layer 5-6 glutamatergic neuron, near-projecting_2 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Layer 5-6 glutamatergic neuron, near-projecting_2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Layer 5-6 glutamatergic neuron, near-projecting_3 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Layer 5-6 glutamatergic neuron, near-projecting_3 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Cpa6+ Layer 6 glutamatergic neuron, corticothalamic-projecting Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Cpa6+ Layer 6 glutamatergic neuron, corticothalamic-projecting cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Gpr139+ Layer 6 glutamatergic neuron, corticothalamic-projecting Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Gpr139+ Layer 6 glutamatergic neuron, corticothalamic-projecting cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Grp+ Layer 6 glutamatergic neuron, corticothalamic-projecting Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Grp+ Layer 6 glutamatergic neuron, corticothalamic-projecting cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Kit+ Layer 6 glutamatergic neuron, corticothalamic-projecting_1 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Kit+ Layer 6 glutamatergic neuron, corticothalamic-projecting_1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Kit+ Layer 6 glutamatergic neuron, corticothalamic-projecting_2 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Kit+ Layer 6 glutamatergic neuron, corticothalamic-projecting_2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Pou3f2+ Layer 6 glutamatergic neuron, corticothalamic-projecting Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Pou3f2+ Layer 6 glutamatergic neuron, corticothalamic-projecting cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Car3+ glutamatergic neuron, intratelencephalon-projecting Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Car3+ glutamatergic neuron, intratelencephalon-projecting cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Layer 6 glutamatergic neuron, intratelencephalon-projecting_1 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Layer 6 glutamatergic neuron, intratelencephalon-projecting_1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Layer 6 glutamatergic neuron, intratelencephalon-projecting_2 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Layer 6 glutamatergic neuron, intratelencephalon-projecting_2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Col6a1+ Layer 6b glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Col6a1+ Layer 6b glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Kcnip1+ Layer 6b glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Kcnip1+ Layer 6b glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Ror1+ Layer 6b glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Ror1+ Layer 6b glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Lamp5+ Lhx6+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Lamp5+ Lhx6+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Lamp5+ Pax6+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Lamp5+ Pax6+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Lamp5+ Slc35d3+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Lamp5+ Slc35d3+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Meis2+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Meis2+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Meis2+ Top2a+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Meis2+ Top2a+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Pvalb+ Egfem1+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Pvalb+ Egfem1+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Pvalb+ Gabrg1+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Pvalb+ Gabrg1+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Pvalb+ Gpr149+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Pvalb+ Gpr149+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Pvalb+ Il1rapl2+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Pvalb+ Il1rapl2+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Pvalb+ Kank4+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Pvalb+ Kank4+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Pvalb+ Reln+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Pvalb+ Reln+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Sncg+ Col14a1+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Sncg+ Col14a1+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Sncg+ Npy2r+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Sncg+ Npy2r+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Sncg+ Slc17a8+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Sncg+ Slc17a8+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Sst+ Calb2+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Sst+ Calb2+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Sst+ Chodl+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Sst+ Chodl+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Sst+ Hpse+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Sst+ Hpse+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Sst+ Htr1a+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Sst+ Htr1a+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Sst+ Penk+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Sst+ Penk+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Sst+ Pvalb+ Calb2+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Sst+ Pvalb+ Calb2+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Sst+ Pvalb+ Etv1+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Sst+ Pvalb+ Etv1+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Sst+ Tac2+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Sst+ Tac2+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Sst+ Pappa+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Sst+ Pappa+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Vip+ C1ql1+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Vip+ C1ql1+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Vip+ Gpc3+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Vip+ Gpc3+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cluster - Sncg+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cluster - Sncg+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cross-Species Cluster - Chandelier neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cross-Species Cluster - Chandelier neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cross-Species Cluster - Layer 2-3 glutamatergic neuron, intratelencephalon-projecting Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cross-Species Cluster - Layer 2-3 glutamatergic neuron, intratelencephalon-projecting cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cross-Species Cluster - Layer 5 glutamatergic neuron, extratelencephalon-projecting_1 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cross-Species Cluster - Layer 5 glutamatergic neuron, extratelencephalon-projecting_1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cross-Species Cluster - Layer 5 glutamatergic neuron, extratelencephalon-projecting_2 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cross-Species Cluster - Layer 5 glutamatergic neuron, extratelencephalon-projecting_2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cross-Species Cluster - Layer 5 glutamatergic neuron, intratelencephalon-projecting_1 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cross-Species Cluster - Layer 5 glutamatergic neuron, intratelencephalon-projecting_1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cross-Species Cluster - Layer 5 glutamatergic neuron, intratelencephalon-projecting_2 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cross-Species Cluster - Layer 5 glutamatergic neuron, intratelencephalon-projecting_2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cross-Species Cluster - Layer 5 glutamatergic neuron, intratelencephalon-projecting_3 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cross-Species Cluster - Layer 5 glutamatergic neuron, intratelencephalon-projecting_3 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cross-Species Cluster - Layer 5-6 glutamatergic neuron, near-projecting Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cross-Species Cluster - Layer 5-6 glutamatergic neuron, near-projecting cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cross-Species Cluster - Layer 6 glutamatergic neuron, corticothalamic-projecting_1 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cross-Species Cluster - Layer 6 glutamatergic neuron, corticothalamic-projecting_1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cross-Species Cluster - Layer 6 glutamatergic neuron, corticothalamic-projecting_2 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cross-Species Cluster - Layer 6 glutamatergic neuron, corticothalamic-projecting_2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cross-Species Cluster - Layer 6 glutamatergic neuron, intratelencephalon-projecting_1 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cross-Species Cluster - Layer 6 glutamatergic neuron, intratelencephalon-projecting_1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cross-Species Cluster - Layer 6 glutamatergic neuron, intratelencephalon-projecting_2 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cross-Species Cluster - Layer 6 glutamatergic neuron, intratelencephalon-projecting_2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cross-Species Cluster - Layer 6 glutamatergic neuron, intratelencephalon-projecting_3 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cross-Species Cluster - Layer 6 glutamatergic neuron, intratelencephalon-projecting_3 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cross-Species Cluster - Layer 6b glutamatergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cross-Species Cluster - Layer 6b glutamatergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Mouse - Motor Cortex - Cross-Species Cluster - Sst+ Chodl+ GABAergic neuron Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Mouse - Motor Cortex - Cross-Species Cluster - Sst+ Chodl+ GABAergic neuron cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
motor neuron pool_Spinal cord_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the motor neuron pool_Spinal cord_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
motor neuron axon guidance Gene SetFrom GO Biological Process Annotations 2025 genes participating in the motor neuron axon guidance biological process from the curated GO Biological Process Annotations 2025 dataset. |
motor neuron migration Gene SetFrom GO Biological Process Annotations 2025 genes participating in the motor neuron migration biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of motor neuron apoptotic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of motor neuron apoptotic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
fasciculation of motor neuron axon Gene SetFrom GO Biological Process Annotations 2025 genes participating in the fasciculation of motor neuron axon biological process from the curated GO Biological Process Annotations 2025 dataset. |
lateral motor column neuron migration Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lateral motor column neuron migration biological process from the curated GO Biological Process Annotations 2025 dataset. |
spinal cord motor neuron differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the spinal cord motor neuron differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of motor neuron apoptotic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of motor neuron apoptotic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
visceral motor neuron differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the visceral motor neuron differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
motor neuron apoptotic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the motor neuron apoptotic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
spinal cord motor neuron cell fate specification Gene SetFrom GO Biological Process Annotations 2025 genes participating in the spinal cord motor neuron cell fate specification biological process from the curated GO Biological Process Annotations 2025 dataset. |
spinal cord motor neuron migration Gene SetFrom GO Biological Process Annotations 2025 genes participating in the spinal cord motor neuron migration biological process from the curated GO Biological Process Annotations 2025 dataset. |
Motor neuron disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Motor neuron disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Motor neuron disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Motor neuron disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Motor neuron disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Motor neuron disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hereditary motor neuron disease Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary motor neuron disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Motor neuron disease Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Motor neuron disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Lower motor neuron syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Lower motor neuron syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
ALS2-related motor neuron disease Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the ALS2-related motor neuron disease phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
neuron projection extension involved in neuron projection guidance Gene SetFrom GO Biological Process Annotations 2015 genes participating in the neuron projection extension involved in neuron projection guidance biological process from the curated GO Biological Process Annotations 2015 dataset. |
neuron-neuron synaptic transmission Gene SetFrom GO Biological Process Annotations 2015 genes participating in the neuron-neuron synaptic transmission biological process from the curated GO Biological Process Annotations 2015 dataset. |
neuron-neuron synaptic transmission Gene SetFrom GO Biological Process Annotations 2023 genes participating in the neuron-neuron synaptic transmission biological process from the curated GO Biological Process Annotations 2023 dataset. |
neuron projection extension involved in neuron projection guidance Gene SetFrom GO Biological Process Annotations 2023 genes participating in the neuron projection extension involved in neuron projection guidance biological process from the curated GO Biological Process Annotations 2023 dataset. |
neuron to neuron synapse Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the neuron to neuron synapse cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
neuron-neuron synaptic transmission Gene SetFrom GO Biological Process Annotations 2025 genes participating in the neuron-neuron synaptic transmission biological process from the curated GO Biological Process Annotations 2025 dataset. |
neuron projection extension involved in neuron projection guidance Gene SetFrom GO Biological Process Annotations 2025 genes participating in the neuron projection extension involved in neuron projection guidance biological process from the curated GO Biological Process Annotations 2025 dataset. |
neuron to neuron synapse Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the neuron to neuron synapse cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
Neuron to neuron synapse Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Neuron to neuron synapse cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Neuron to neuron synapse Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Neuron to neuron synapse cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Muscle Weakness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Muscle Weakness from the curated CTD Gene-Disease Associations dataset. |
Episodic Muscle Weakness, X-Linked Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Episodic Muscle Weakness, X-Linked from the curated CTD Gene-Disease Associations dataset. |
deglutition disorders; muscle weakness; myositis, inclusion body Gene SetFrom GAD Gene-Disease Associations genes associated with the disease deglutition disorders; muscle weakness; myositis, inclusion body in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
weakness Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term weakness in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
abdominal wall muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the abdominal wall muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
foot dorsiflexor weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the foot dorsiflexor weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
peroneal muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the peroneal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
late-onset distal muscle weakness Gene SetFrom 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. |
limb muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the limb muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
first dorsal interossei muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the first dorsal interossei muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
episodic flaccid weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the episodic flaccid weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
late-onset proximal muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the late-onset proximal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
scapuloperoneal weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the scapuloperoneal weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
progressive muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the progressive muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
shoulder girdle muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the shoulder girdle muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal lower limb muscle weakness Gene SetFrom 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. |
weakness of long finger extensor muscles Gene SetFrom HPO Gene-Disease Associations genes associated with the weakness of long finger extensor muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neck flexor weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the neck flexor weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
weakness of the intrinsic hand muscles Gene SetFrom HPO Gene-Disease Associations genes associated with the weakness of the intrinsic hand muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neck muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the neck muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
intercostal muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the intercostal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
lower limb muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the lower limb muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal muscle weakness in lower limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal muscle weakness in lower limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
weakness of muscles of respiration Gene SetFrom HPO Gene-Disease Associations genes associated with the weakness of muscles of respiration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
generalized muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the generalized muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
progressive proximal muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the progressive proximal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
diaphragmatic weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the diaphragmatic weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
fatigable weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the fatigable weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal muscle weakness Gene SetFrom 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. |
thenar muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the thenar muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
quadriceps muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the quadriceps muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pelvic girdle muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the pelvic girdle muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
axial muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the axial muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
progressive distal muscle weakness Gene SetFrom 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. |
limb-girdle muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the limb-girdle muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hand muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the hand muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Muscle Weakness Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Muscle Weakness phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
progressive muscle weakness Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the progressive muscle weakness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
muscle weakness Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the muscle weakness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
weakness Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the weakness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness Gene SetFrom OMIM Gene-Disease Associations genes associated with the ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness phenotype from the curated OMIM Gene-Disease Associations dataset. |
episodic muscle weakness, x-linked Gene SetFrom OMIM Gene-Disease Associations genes associated with the episodic muscle weakness, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset. |
Bulbar Weakness Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bulbar Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bilateral Facial Muscle Weakness Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bilateral Facial Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Muscle Weakness Gene SetFrom 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. |
Foot Dorsiflexor Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Foot Dorsiflexor Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Generalized Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Generalized Muscle Weakness, Ctcae Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Muscle Weakness, Ctcae in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Progressive Proximal Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Proximal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Shoulder Girdle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Shoulder Girdle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fatigable Weakness Of Neck Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fatigable Weakness Of Neck Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Proximal Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Axial Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Axial Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fatigable Weakness Of Bulbar Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fatigable Weakness Of Bulbar Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fatigable Weakness Of Distal Limb Muscles Gene SetFrom 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. |
Fatigable Weakness Of Respiratory Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fatigable Weakness Of Respiratory Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fatiguable Weakness Of Proximal Limb Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fatiguable Weakness Of Proximal Limb Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Late-Onset Distal Muscle Weakness Gene SetFrom 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. |
Limb-Girdle Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Limb-Girdle Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Muscle Weakness Of Limb Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscle Weakness Of Limb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Neck Flexor Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neck Flexor Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Neck Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neck Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Progressive Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Generalized Weakness Of Limb Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Weakness Of Limb Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Lower Limb Muscle Weakness Gene SetFrom 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. |
Facial Muscle Weakness Of Muscles Innervated By Cn Vii Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Facial Muscle Weakness Of Muscles Innervated By Cn Vii in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Quadriceps Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Quadriceps Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Triceps Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Triceps Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Ankle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ankle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Frontalis Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Frontalis Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hip Flexor Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hip Flexor Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Weakness Of Long Finger Extensor Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Weakness Of Long Finger Extensor Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Weakness Of The Intrinsic Hand Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Weakness Of The Intrinsic Hand Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Favorable Response Of Weakness To Acetylcholine Esterase Inhibitors Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Favorable Response Of Weakness To Acetylcholine Esterase Inhibitors in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fatigable Weakness Of Swallowing Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fatigable Weakness Of Swallowing Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Calf Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Calf Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pelvic Girdle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pelvic Girdle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Proximal Muscle Weakness In Lower Limbs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Muscle Weakness In Lower Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hand Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hand Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
First Dorsal Interossei Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype First Dorsal Interossei Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Thenar Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thenar Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Tibialis Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tibialis Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Episodic Flaccid Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Flaccid Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Late-Onset Proximal Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Late-Onset Proximal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abdominal Wall Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abdominal Wall Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Progressive Distal Muscle Weakness Gene SetFrom 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. |
Proximal Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Unfavorable Response Of Muscle Weakness To Acetylcholine Esterase Inhibitors Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Unfavorable Response Of Muscle Weakness To Acetylcholine Esterase Inhibitors in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Muscle Pain Or Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscle Pain Or Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Weakness Worsened Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Weakness Worsened in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Scapuloperoneal Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Scapuloperoneal Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Finger Flexor Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Finger Flexor Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fatigable Weakness Of Skeletal Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fatigable Weakness Of Skeletal Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Weakness Of Muscles Of Respiration Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Weakness Of Muscles Of Respiration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Intercostal Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Intercostal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Peroneal Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peroneal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Weakness Of Orbicularis Oculi Muscle Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Weakness Of Orbicularis Oculi Muscle in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fatigable Weakness Of Speech Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fatigable Weakness Of Speech Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
weakness Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the weakness phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
muscle weakness Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the muscle weakness phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
progressive muscle weakness Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the progressive muscle weakness phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Lower limb muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Lower limb muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Progressive distal muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive distal muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Progressive proximal muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive proximal muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal muscle weakness Gene SetFrom 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 SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal lower limb muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Shoulder girdle muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Shoulder girdle muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Limb-girdle muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Limb-girdle muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Scapuloperoneal weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Scapuloperoneal weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Generalized muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Generalized muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Pelvic girdle muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Pelvic girdle muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Proximal muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Proximal muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Episodic flaccid weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Episodic flaccid weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hip flexor weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hip flexor weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Proximal muscle weakness in lower limbs Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Proximal muscle weakness in lower limbs phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Progressive muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Foot dorsiflexor weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Foot dorsiflexor weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Primary somatosensory area, upper limb, layer 2/3 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, upper limb, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
upper dorsal perifornical nucleus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in upper dorsal perifornical nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, upper limb Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, upper limb relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
upper dorsal lateral hypothalamic area Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in upper dorsal lateral hypothalamic area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
upper basal perifornical nucleus Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in upper basal perifornical nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, upper limb, layer 1 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, upper limb, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, upper limb, layer 5 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, upper limb, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, upper limb, layer 4 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, upper limb, layer 4 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, upper limb, layer 6a Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, upper limb, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Primary somatosensory area, upper limb, layer 6b Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Primary somatosensory area, upper limb, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
upper basal lateral hypothalamic area Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in upper basal lateral hypothalamic area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
upper (rostral) rhombic lip_8 pcw_M_13058 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in upper (rostral) rhombic lip_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
upper (rostral) rhombic lip_9 pcw_M_12833 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in upper (rostral) rhombic lip_9 pcw_M_12833 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset. |
upper (rostral) rhombic lip_9 pcw_M_12833 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in upper (rostral) rhombic lip_9 pcw_M_12833 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
upper (rostral) rhombic lip_8 pcw_M_13058 Gene SetFrom Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in upper (rostral) rhombic lip_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset. |
upper limb region of M1 Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in upper limb region of M1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
external granular (germinal) layer of upper rhombic lip Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in external granular (germinal) layer of upper rhombic lip relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
upper (rostral) rhombic lip Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in upper (rostral) rhombic lip relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
Single upper central incisor Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Single upper central incisor phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Single upper central incisor Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Single upper central incisor from the curated CTD Gene-Disease Associations dataset. |
upper respiratory tract disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease upper respiratory tract disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
upper respiratory tract disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease upper respiratory tract disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
mononeuritis of upper limb and mononeuritis multiplex Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease mononeuritis of upper limb and mononeuritis multiplex in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
H3K4me3_fibroblast of upper leg skin_hg19_1 Gene SetFrom ENCODE Histone Modification Site Profiles genes with high histone modification abundance in the H3K4me3_fibroblast of upper leg skin_hg19_1 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset. |
H3K4me3_fibroblast of upper leg skin_hg19_2 Gene SetFrom ENCODE Histone Modification Site Profiles genes with high histone modification abundance in the H3K4me3_fibroblast of upper leg skin_hg19_2 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset. |
CTCF_fibroblast of upper leg skin_hg19_2 Gene SetFrom ENCODE Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CTCF_fibroblast of upper leg skin_hg19_2 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset. |
CTCF_fibroblast of upper leg skin_hg19_1 Gene SetFrom ENCODE Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CTCF_fibroblast of upper leg skin_hg19_1 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset. |
adenocarcinoma of the upper gastrointestinal tract. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma of the upper gastrointestinal tract. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
tumours of the upper aerodigestive tract Gene SetFrom GAD Gene-Disease Associations genes associated with the disease tumours of the upper aerodigestive tract in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
upper aerodigestive tract cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease upper aerodigestive tract cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
neoplasms; recurrence; thromboembolism; thrombophilia; upper extremity deep vein thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease neoplasms; recurrence; thromboembolism; thrombophilia; upper extremity deep vein thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
upper aerodigestive tract cancers Gene SetFrom GAD Gene-Disease Associations genes associated with the disease upper aerodigestive tract cancers in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
upper Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term upper in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Bone mineral density (paediatric, upper limb) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Bone mineral density (paediatric, upper limb) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Upper aerodigestive tract cancers Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Upper aerodigestive tract cancers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
upper respiratory tract disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease upper respiratory tract disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
abnormality of upper limb bone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of upper limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
diaphyseal sclerosis of the upper limbs Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the diaphyseal sclerosis of the upper limbs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the upper urinary tract Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the upper urinary tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the upper limb Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the upper limb phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of upper limb metaphysis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of upper limb metaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
sclerosis of metaphyses of the upper limbs Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the sclerosis of metaphyses of the upper limbs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the upper arm Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the upper arm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
anomaly of the upper limb diaphyses Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the anomaly of the upper limb diaphyses phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of upper lip Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased upper to lower segment ratio Gene SetFrom HPO Gene-Disease Associations genes associated with the increased upper to lower segment ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the musculature of the upper arm Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the musculature of the upper arm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper limb bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper limb bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
u-shaped upper lip vermilion Gene SetFrom HPO Gene-Disease Associations genes associated with the u-shaped upper lip vermilion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
upper limb metaphyseal widening Gene SetFrom HPO Gene-Disease Associations genes associated with the upper limb metaphyseal widening phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the musculature of the upper limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the musculature of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
tented upper lip vermilion Gene SetFrom HPO Gene-Disease Associations genes associated with the tented upper lip vermilion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the upper limb Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the upper limb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper limb epiphysis morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper limb epiphysis morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the upper arm Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the upper arm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cleft upper lip Gene SetFrom HPO Gene-Disease Associations genes associated with the cleft upper lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper limb metaphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper limb metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
everted upper lip vermilion Gene SetFrom HPO Gene-Disease Associations genes associated with the everted upper lip vermilion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
upper eyelid coloboma Gene SetFrom HPO Gene-Disease Associations genes associated with the upper eyelid coloboma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hyporeflexia of upper limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the hyporeflexia of upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper limb joint Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper limb joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
duplication of bones involving the upper extremities Gene SetFrom HPO Gene-Disease Associations genes associated with the duplication of bones involving the upper extremities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the musculature of the upper arm Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the musculature of the upper arm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short upper lip Gene SetFrom HPO Gene-Disease Associations genes associated with the short upper lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
synostosis involving bones of the upper limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the synostosis involving bones of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
upper limb postural tremor Gene SetFrom HPO Gene-Disease Associations genes associated with the upper limb postural tremor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal upper limb amyotrophy Gene SetFrom 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. |
abnormal morphology of bones of the upper limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal morphology of bones of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
upper limb amyotrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the upper limb amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
upper limb phocomelia Gene SetFrom HPO Gene-Disease Associations genes associated with the upper limb phocomelia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent upper and lower respiratory tract infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent upper and lower respiratory tract infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving bones of the upper limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving bones of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long upper lip Gene SetFrom HPO Gene-Disease Associations genes associated with the long upper lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
upper limb spasticity Gene SetFrom HPO Gene-Disease Associations genes associated with the upper limb spasticity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal upper limb amyotrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal upper limb amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal upper to lower segment ratio Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal upper to lower segment ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
episodic upper airway obstruction Gene SetFrom HPO Gene-Disease Associations genes associated with the episodic upper airway obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thick upper lip vermilion Gene SetFrom HPO Gene-Disease Associations genes associated with the thick upper lip vermilion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the upper respiratory tract Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the upper respiratory tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
flared upper limb metaphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the flared upper limb metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper lip vermillion Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper lip vermillion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thin upper lip vermilion Gene SetFrom HPO Gene-Disease Associations genes associated with the thin upper lip vermilion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent upper respiratory tract infections Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent upper respiratory tract infections phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
upper airway obstruction Gene SetFrom HPO Gene-Disease Associations genes associated with the upper airway obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
upper limb undergrowth Gene SetFrom HPO Gene-Disease Associations genes associated with the upper limb undergrowth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the upper urinary tract Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the upper urinary tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia involving bones of the upper limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia involving bones of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
contractures of the joints of the upper limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the contractures of the joints of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the musculature of the upper limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the musculature of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
upper limb muscle hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the upper limb muscle hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
upper extremity joint dislocation Gene SetFrom HPO Gene-Disease Associations genes associated with the upper extremity joint dislocation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Upper Extremity Deformities, Congenital Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Upper Extremity Deformities, Congenital phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Upper Extremity Deep Vein Thrombosis Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Upper Extremity Deep Vein Thrombosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
absent upper incisors Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent upper incisors phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal upper lip morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal upper lip morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
upper epidermis Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue upper epidermis in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Upper Limb Asymmetry Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Upper Limb Asymmetry in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Recurrent Upper Respiratory Tract Infection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Recurrent Upper Respiratory Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Upper Limb Amyotrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Upper Limb Amyotrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cortical Diaphyseal Thickening Of The Upper Limbs Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cortical Diaphyseal Thickening Of The Upper Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Upper Airway Obstruction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Upper Airway Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Upper Urinary Tract Infection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Upper Urinary Tract Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Upper Limb Peromelia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Upper Limb Peromelia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Upper Limb Amyotrophy Gene SetFrom 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. |
Acute Upper Respiratory Infection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acute Upper Respiratory Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Upper Gastrointestinal Symptoms Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Upper Gastrointestinal Symptoms in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Upper Airway Resistance Sleep Apnea Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Upper Airway Resistance Sleep Apnea Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Upper Gi Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Upper Gi Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Upper Extremity Deep Vein Thrombosis, Primary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Upper Extremity Deep Vein Thrombosis, Primary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of Upper Lip Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Upper Lip in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Phocomelia Of Upper Limb Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Phocomelia Of Upper Limb in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of Upper Lip Vermillion Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Upper Lip Vermillion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thick Upper Lip Vermilion Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thick Upper Lip Vermilion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Right Upper Quadrant Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Right Upper Quadrant Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Thin Upper Lip Vermilion Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thin Upper Lip Vermilion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Tented Upper Lip Vermilion Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tented Upper Lip Vermilion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Upper Limb Spasticity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Limb Spasticity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Upper Limb Hypertonia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Limb Hypertonia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Recurrent Upper And Lower Respiratory Tract Infections Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Recurrent Upper And Lower Respiratory Tract Infections in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hyperreflexia In Upper Limbs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hyperreflexia In Upper Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Upper Lip Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Upper Lip in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Upper Limb Postural Tremor Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Limb Postural Tremor in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Everted Upper Lip Vermilion Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Everted Upper Lip Vermilion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of The Upper Limb Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Upper Limb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Long Upper Lip Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Long Upper Lip in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hyporeflexia Of Upper Limbs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hyporeflexia Of Upper Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
U-Shaped Upper Lip Vermilion Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype U-Shaped Upper Lip Vermilion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Upper Extremity Paresis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Extremity Paresis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Upper Abdominal Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Abdominal Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Midline Notch Of Upper Alveolar Ridge Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Midline Notch Of Upper Alveolar Ridge in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of The Upper Urinary Tract Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Upper Urinary Tract in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Proximal Upper Limb Amyotrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Upper Limb Amyotrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Episodic Upper Airway Obstruction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Episodic Upper Airway Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Upper To Lower Segment Ratio Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Upper To Lower Segment Ratio in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Upper Limb Dysmetria Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Limb Dysmetria in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Upper Back Pain Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Back Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Upper Limb Muscle Hypertrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Limb Muscle Hypertrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Proximal Upper Limb Muscle Hypertrophy Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Upper Limb Muscle Hypertrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Loss Of Subcutaneous Adipose Tissue From Upper Limbs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Subcutaneous Adipose Tissue From Upper Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Osteolysis Involving Bones Of The Upper Limbs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Osteolysis Involving Bones Of The Upper Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Upper To Lower Segment Ratio Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Upper To Lower Segment Ratio in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Upper Limb Muscle Hypoplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Limb Muscle Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Upper Lip Pit Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Upper Lip Pit in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Upper Limb Bone Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Upper Limb Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Upper Limb Joint Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Upper Limb Joint in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
short upper incisors Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short upper incisors phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
lower jaw to upper jaw transformation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the lower jaw to upper jaw transformation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent upper incisors Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent upper incisors phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal upper incisor morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal upper incisor morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
cleft upper lip Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the cleft upper lip phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
unilateral cleft upper lip Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the unilateral cleft upper lip phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
bilateral cleft upper lip Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the bilateral cleft upper lip phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long upper incisors Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long upper incisors phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal upper lip morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal upper lip morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal upper incisor color Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal upper incisor color phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
midline cleft upper lip Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the midline cleft upper lip phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thin upper lip Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thin upper lip phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
fused upper incisors Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the fused upper incisors phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick upper lip Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick upper lip phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
upper jaw to lower jaw transformation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the upper jaw to lower jaw transformation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
small upper incisors Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the small upper incisors phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Upper neuron_Brain_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Upper neuron_Brain_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Upper layer cell_Prefrontal cortex_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Upper layer cell_Prefrontal cortex_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Upper layer cortical neuron_Cortex_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Upper layer cortical neuron_Cortex_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Upper layer 2 cell_Primary visual cortex_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Upper layer 2 cell_Primary visual cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Upper layer 3 cell_Primary visual cortex_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Upper layer 3 cell_Primary visual cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Upper layer 4 cell_Primary visual cortex_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Upper layer 4 cell_Primary visual cortex_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Upper Wound Fibroblast_Skin_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Upper Wound Fibroblast_Skin_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Upper respiratory tract disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Upper respiratory tract disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Upper respiratory tract disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Upper respiratory tract disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Mononeuritis of upper limb and mononeuritis multiplex Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Mononeuritis of upper limb and mononeuritis multiplex in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Diplegia of upper limb Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Diplegia of upper limb in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Upper lip cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Upper lip cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Upper epidermis Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Upper epidermis in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Upper tip-link density Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Upper tip-link density cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Finnish upper limb-onset distal myopathy Gene SetFrom 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. |
Facial morphology (factor 17, height of vermillion upper lip) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Facial morphology (factor 17, height of vermillion upper lip) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Bone mineral density (paediatric, upper limb) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bone mineral density (paediatric, upper limb) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Upper eyelid sagging severity Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Upper eyelid sagging severity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Upper eyelid morphology Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Upper eyelid morphology phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Sinoatrial node dysfunction and deafness Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sinoatrial node dysfunction and deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Surfactant metabolism dysfunction, pulmonary, 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Surfactant metabolism dysfunction, pulmonary, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hirschsprung disease, cardiac defects, and autonomic dysfunction Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Surfactant metabolism dysfunction, pulmonary, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Surfactant metabolism dysfunction, pulmonary, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Surfactant metabolism dysfunction, pulmonary, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Surfactant metabolism dysfunction, pulmonary, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Surfactant metabolism dysfunction, pulmonary, 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Surfactant metabolism dysfunction, pulmonary, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Arthrogryposis, renal dysfunction, and cholestasis 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, renal dysfunction, and cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Surfactant metabolism dysfunction, pulmonary, 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Surfactant metabolism dysfunction, pulmonary, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Sensorineural deafness with mild renal dysfunction Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Sensorineural deafness with mild renal dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Arthrogryposis renal dysfunction cholestasis syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis renal dysfunction cholestasis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE) Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE) phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ventricular Dysfunction Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ventricular Dysfunction from the curated CTD Gene-Disease Associations dataset. |
Phagocyte Bactericidal Dysfunction Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Phagocyte Bactericidal Dysfunction from the curated CTD Gene-Disease Associations dataset. |
Temporomandibular Joint Dysfunction Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Temporomandibular Joint Dysfunction Syndrome from the curated CTD Gene-Disease Associations dataset. |
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY from the curated CTD Gene-Disease Associations dataset. |
Maturity-Onset Diabetes of the Young, Type 8, with Exocrine Dysfunction Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Maturity-Onset Diabetes of the Young, Type 8, with Exocrine Dysfunction from the curated CTD Gene-Disease Associations dataset. |
Ventricular Dysfunction, Left Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ventricular Dysfunction, Left from the curated CTD Gene-Disease Associations dataset. |
Sexual Dysfunction, Physiological Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sexual Dysfunction, Physiological from the curated CTD Gene-Disease Associations dataset. |
Erectile Dysfunction Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Erectile Dysfunction from the curated CTD Gene-Disease Associations dataset. |
Ventricular Dysfunction, Right Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Ventricular Dysfunction, Right from the curated CTD Gene-Disease Associations dataset. |
Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis from the curated CTD Gene-Disease Associations dataset. |
Surfactant Metabolism Dysfunction, Pulmonary, 1 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Surfactant Metabolism Dysfunction, Pulmonary, 1 from the curated CTD Gene-Disease Associations dataset. |
Surfactant Metabolism Dysfunction, Pulmonary, 2 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Surfactant Metabolism Dysfunction, Pulmonary, 2 from the curated CTD Gene-Disease Associations dataset. |
Surfactant Metabolism Dysfunction, Pulmonary, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Surfactant Metabolism Dysfunction, Pulmonary, 4 from the curated CTD Gene-Disease Associations dataset. |
Arthrogryposis renal dysfunction cholestasis syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Arthrogryposis renal dysfunction cholestasis syndrome from the curated CTD Gene-Disease Associations dataset. |
Surfactant Metabolism Dysfunction, Pulmonary, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Surfactant Metabolism Dysfunction, Pulmonary, 3 from the curated CTD Gene-Disease Associations dataset. |
Sphincter of Oddi Dysfunction Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Sphincter of Oddi Dysfunction from the curated CTD Gene-Disease Associations dataset. |
Erectile Dysfunction Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Erectile Dysfunction in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
phagocyte bactericidal dysfunction Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease phagocyte bactericidal dysfunction from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
sexual dysfunction Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease sexual dysfunction in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
labyrinthine dysfunction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease labyrinthine dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
phagocyte bactericidal dysfunction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease phagocyte bactericidal dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
bowel dysfunction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease bowel dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
ovarian dysfunction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ovarian dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
sexual dysfunction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease sexual dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
cardiovascular diseases; ventricular dysfunction, left Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary artery disease; erectile dysfunction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary artery disease; erectile dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ovarian dysfunction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ovarian dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
physiological sexual disorders; sexual dysfunction, physiological Gene SetFrom GAD Gene-Disease Associations genes associated with the disease physiological sexual disorders; sexual dysfunction, physiological in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ventricular dysfunction, left Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obesity; ventricular dysfunction, left Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obesity; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sexual dysfunction, physiological Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sexual dysfunction, physiological in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; ventricular dysfunction, left Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; hypertrophy, left ventricular; kidney failure, chronic; left ventricular hypertrophy; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ventricular dysfunction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ventricular dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
allograft dysfunction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease allograft dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
heart failure; inflammation; ventricular dysfunction, left Gene SetFrom GAD Gene-Disease Associations genes associated with the disease heart failure; inflammation; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular; ventricular dysfunction, left Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, hypertrophic, familial; hypertrophy, left ventricular; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiomyopathy, dilated; dcm - dilated cardiomyopathy; heart failure; hemochromatosis; ventricular dysfunction, left Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; dcm - dilated cardiomyopathy; heart failure; hemochromatosis; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary atresia; liver diseases; primary graft dysfunction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary atresia; liver diseases; primary graft dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
delayed graft function acute rejection episodes and long-term graft dysfunction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease delayed graft function acute rejection episodes and long-term graft dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
beta thalassemia; beta-thalassemia; ventricular dysfunction, left Gene SetFrom GAD Gene-Disease Associations genes associated with the disease beta thalassemia; beta-thalassemia; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes complications; erectile dysfunction; hypogonadism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes complications; erectile dysfunction; hypogonadism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
erectile dysfunction; metabolic syndrome x Gene SetFrom GAD Gene-Disease Associations genes associated with the disease erectile dysfunction; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
endothelial dysfunction in normal humans. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease endothelial dysfunction in normal humans. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
left ventricular dysfunction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease left ventricular dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; autonomic nervous system dysfunction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; autonomic nervous system dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiomyopathy, dilated; inflammation; myocarditis; ventricular dysfunction, left Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiomyopathy, dilated; inflammation; myocarditis; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sepsis-related organ dysfunction and shock after burn injury Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sepsis-related organ dysfunction and shock after burn injury in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
erectile dysfunction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease erectile dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic; ventricular dysfunction, left Gene SetFrom GAD Gene-Disease Associations genes associated with the disease chronic renal failure; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; diabetic nephropathies; diabetic nephropathy; kidney failure, chronic; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
heart failure; ventricular dysfunction, left Gene SetFrom GAD Gene-Disease Associations genes associated with the disease heart failure; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; hypertrophy, left ventricular; left ventricular hypertrophy; ventricular dysfunction, left Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; hypertrophy, left ventricular; left ventricular hypertrophy; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myocardial infarction; ventricular dysfunction, left Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial infarction; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
temporomandibular dysfunction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease temporomandibular dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis; coronary vascular endothelial dysfunction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis; coronary vascular endothelial dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myocardial infarct; coronary endothelial vasomotor dysfunction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myocardial infarct; coronary endothelial vasomotor dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
kidney dysfunction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease kidney dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
fatigue; ventricular dysfunction, left Gene SetFrom GAD Gene-Disease Associations genes associated with the disease fatigue; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; heart failure; inflammation; ventricular dysfunction Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; heart failure; inflammation; ventricular dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypertension; renal dysfunction, posttransplantation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypertension; renal dysfunction, posttransplantation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
heart failure; ventricular dysfunction, left; ventricular remodeling Gene SetFrom GAD Gene-Disease Associations genes associated with the disease heart failure; ventricular dysfunction, left; ventricular remodeling in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
aortic valve stenosis; hypertrophy, left ventricular; left ventricular hypertrophy; ventricular dysfunction, left Gene SetFrom GAD Gene-Disease Associations genes associated with the disease aortic valve stenosis; hypertrophy, left ventricular; left ventricular hypertrophy; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
allograft dysfunction, renal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease allograft dysfunction, renal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hypercholesterolemia; myocardial infarction; ventricular dysfunction, left Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hypercholesterolemia; myocardial infarction; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis, coronary; myocardial dysfunction, non-ischaemic Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis, coronary; myocardial dysfunction, non-ischaemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
heart diseases; ventricular dysfunction, left Gene SetFrom GAD Gene-Disease Associations genes associated with the disease heart diseases; ventricular dysfunction, left in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dysfunction Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term dysfunction in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Erectile dysfunction and prostate cancer treatment Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Erectile dysfunction and prostate cancer treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Sexual dysfunction (SSRI/SNRI-related) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Sexual dysfunction (SSRI/SNRI-related) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Erectile dysfunction Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Erectile dysfunction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Sexual dysfunction (female) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Sexual dysfunction (female) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
sexual dysfunction Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease sexual dysfunction in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
muscle abnormality related to mitochondrial dysfunction Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the muscle abnormality related to mitochondrial dysfunction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
autonomic bladder dysfunction Gene SetFrom HPO Gene-Disease Associations genes associated with the autonomic bladder dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
muscle abnormality related to mitochondrial dysfunction Gene SetFrom HPO Gene-Disease Associations genes associated with the muscle abnormality related to mitochondrial dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
beta-cell dysfunction Gene SetFrom HPO Gene-Disease Associations genes associated with the beta-cell dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
vestibular dysfunction Gene SetFrom HPO Gene-Disease Associations genes associated with the vestibular dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
gallbladder dysfunction Gene SetFrom HPO Gene-Disease Associations genes associated with the gallbladder dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
autonomic erectile dysfunction Gene SetFrom HPO Gene-Disease Associations genes associated with the autonomic erectile dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
urinary bladder sphincter dysfunction Gene SetFrom HPO Gene-Disease Associations genes associated with the urinary bladder sphincter dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
renal tubular dysfunction Gene SetFrom HPO Gene-Disease Associations genes associated with the renal tubular dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Ventricular Dysfunction Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Ventricular Dysfunction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Posterior Tibial Tendon Dysfunction Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Posterior Tibial Tendon Dysfunction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Ventricular Dysfunction, Left Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Ventricular Dysfunction, Left phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Primary Graft Dysfunction Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Primary Graft Dysfunction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Sexual Dysfunction, Physiological Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Sexual Dysfunction, Physiological phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Ventricular Dysfunction, Right Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Ventricular Dysfunction, Right phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
hirschsprung disease, cardiac defects, and autonomic dysfunction Gene SetFrom OMIM Gene-Disease Associations genes associated with the hirschsprung disease, cardiac defects, and autonomic dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset. |
multisystemic smooth muscle dysfunction syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the multisystemic smooth muscle dysfunction syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type) Gene SetFrom OMIM Gene-Disease Associations genes associated with the thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type) phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthrogryposis, renal dysfunction, and cholestasis 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthrogryposis, renal dysfunction, and cholestasis 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthrogryposis, renal dysfunction, and cholestasis 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthrogryposis, renal dysfunction, and cholestasis 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovasuclar malformations Gene SetFrom OMIM Gene-Disease Associations genes associated with the infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovasuclar malformations phenotype from the curated OMIM Gene-Disease Associations dataset. |
autonomic nervous system dysfunction Gene SetFrom OMIM Gene-Disease Associations genes associated with the autonomic nervous system dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset. |
retinal dystrophy, early-onset, and pituitary dysfunction Gene SetFrom OMIM Gene-Disease Associations genes associated with the retinal dystrophy, early-onset, and pituitary dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset. |
sinoatrial node dysfunction and deafness Gene SetFrom OMIM Gene-Disease Associations genes associated with the sinoatrial node dysfunction and deafness phenotype from the curated OMIM Gene-Disease Associations dataset. |
thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type) Gene SetFrom OMIM Gene-Disease Associations genes associated with the thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type) phenotype from the curated OMIM Gene-Disease Associations dataset. |
?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset. |
thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2) Gene SetFrom OMIM Gene-Disease Associations genes associated with the thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2) phenotype from the curated OMIM Gene-Disease Associations dataset. |
sensorineural deafness with mild renal dysfunction Gene SetFrom OMIM Gene-Disease Associations genes associated with the sensorineural deafness with mild renal dysfunction phenotype from the curated OMIM Gene-Disease Associations dataset. |
surfactant metabolism dysfunction, pulmonary, 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the surfactant metabolism dysfunction, pulmonary, 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
surfactant metabolism dysfunction, pulmonary, 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the surfactant metabolism dysfunction, pulmonary, 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
surfactant metabolism dysfunction, pulmonary, 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the surfactant metabolism dysfunction, pulmonary, 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
surfactant metabolism dysfunction, pulmonary, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the surfactant metabolism dysfunction, pulmonary, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
surfactant metabolism dysfunction, pulmonary, 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the surfactant metabolism dysfunction, pulmonary, 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
Surfactant Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Surfactant Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Surfactant Metabolism Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Surfactant Metabolism Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Erectile Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Erectile Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dysfunction Adrenal Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dysfunction Adrenal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Testicular Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Testicular Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Coronary Microvascular Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Coronary Microvascular Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Left Ventricular Systolic Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Left Ventricular Systolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Memory Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Memory Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Vasculogenic Erectile Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Vasculogenic Erectile Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Left Ventricular Diastolic Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Left Ventricular Diastolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cerebral Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cerebral Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Placental Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Placental Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bowel Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bowel Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Psychosexual Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Psychosexual Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Minimal Brain Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Minimal Brain Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sleep Initiation Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sleep Initiation Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Neurogenic Bladder Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Neurogenic Bladder Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Organ Dysfunction Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Organ Dysfunction Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Leptin Deficiency Or Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Leptin Deficiency Or Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sinus Node Dysfunction (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sinus Node Dysfunction (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Executive Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Executive Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypothalamic-Pituitary-Adrenal Axis Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypothalamic-Pituitary-Adrenal Axis Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Meibomian Gland Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Meibomian Gland Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Neutrophil Actin Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Neutrophil Actin Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypothalamic Dysfunction Syndromes Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypothalamic Dysfunction Syndromes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Symphysis Pubis Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Symphysis Pubis Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Autonomic Bladder Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Autonomic Bladder Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Female Sexual Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Female Sexual Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Temporomandibular Joint Dysfunction Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Temporomandibular Joint Dysfunction Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sensorineural Deafness With Mild Renal Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sensorineural Deafness With Mild Renal Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pangastrointestinal System Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pangastrointestinal System Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Sinoatrial Node Dysfunction And Deafness Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Sinoatrial Node Dysfunction And Deafness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Colonic Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Colonic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Emotional Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Emotional Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Phagocyte Bactericidal Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Phagocyte Bactericidal Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Male Sexual Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Male Sexual Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hirschsprung Disease, Cardiac Defects, And Autonomic Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hirschsprung Disease, Cardiac Defects, And Autonomic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Segmental Autonomic Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Segmental Autonomic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pineal Gland Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pineal Gland Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Posterior Tibial Tendon Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Posterior Tibial Tendon Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Pyramidal Tract Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Pyramidal Tract Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Severe Left Ventricular Systolic Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Severe Left Ventricular Systolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Nonneurogenic Neurogenic Bladder Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Nonneurogenic Neurogenic Bladder Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Peroxisomal Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Peroxisomal Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Leptin Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Leptin Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Immune Dysfunction With T-Cell Inactivation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Immune Dysfunction With T-Cell Inactivation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Right Ventricular Systolic Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Right Ventricular Systolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thyroid Dysfunction, Postpartum Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thyroid Dysfunction, Postpartum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ischemic Myocardial Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ischemic Myocardial Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Thiamine Metabolism Dysfunction Syndrome 5 (Episodic Encephalopathy Type) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Thiamine Metabolism Dysfunction Syndrome 5 (Episodic Encephalopathy Type) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Facial Palsy, Congenital, With Ptosis And Velopharyngeal Dysfunction Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Facial Palsy, Congenital, With Ptosis And Velopharyngeal Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Endothelial Dysfunction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Endothelial Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Liver Dysfunction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Liver Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Beta-Cell Dysfunction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Beta-Cell Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Urinary Bladder Sphincter Dysfunction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Urinary Bladder Sphincter Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Ventricular Dysfunction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Ventricular Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Postoperative Cognitive Dysfunction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Postoperative Cognitive Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Dysfunction Of Lateral Corticospinal Tracts Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dysfunction Of Lateral Corticospinal Tracts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Neurologic Dysfunction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neurologic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Vestibular Dysfunction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Vestibular Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Gastrointestinal Dysfunction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Gastrointestinal Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Velopharyngeal Dysfunction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Velopharyngeal Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Uterine Dysfunction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Uterine Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Autonomic Erectile Dysfunction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Autonomic Erectile Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Right Ventricular Dysfunction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Right Ventricular Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Autonomic Nervous System Dysfunction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Autonomic Nervous System Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Muscle Abnormality Related To Mitochondrial Dysfunction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Muscle Abnormality Related To Mitochondrial Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Speech Dysfunction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Speech Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Primary Graft Dysfunction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Primary Graft Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Diastolic Dysfunction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Diastolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Left Ventricular Systolic Dysfunction Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Left Ventricular Systolic Dysfunction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
NAD metabolism in oncogene induced senescence and mitochondrial dysfunction associated senescence Gene SetFrom WikiPathways Pathways 2024 proteins participating in the NAD metabolism in oncogene induced senescence and mitochondrial dysfunction associated senescence pathway from the WikiPathways Pathways 2024 dataset. |
SARS CoV 2 mitochondrial chronic oxidative stress and endothelial dysfunction Gene SetFrom WikiPathways Pathways 2024 proteins participating in the SARS CoV 2 mitochondrial chronic oxidative stress and endothelial dysfunction pathway from the WikiPathways Pathways 2024 dataset. |
ROS in COVID 19 endothelial dysfunction Gene SetFrom WikiPathways Pathways 2024 proteins participating in the ROS in COVID 19 endothelial dysfunction pathway from the WikiPathways Pathways 2024 dataset. |
Phagocyte bactericidal dysfunction Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Phagocyte bactericidal dysfunction from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Metabolic dysfunction-associated steatotic liver disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Metabolic dysfunction-associated steatotic liver disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Ovarian dysfunction Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Ovarian dysfunction from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Metabolic dysfunction-associated steatotic liver disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Metabolic dysfunction-associated steatotic liver disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Ovarian dysfunction Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Ovarian dysfunction in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Sexual dysfunction Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Sexual dysfunction in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Metabolic dysfunction and alcohol associated liver disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Metabolic dysfunction and alcohol associated liver disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Ovarian dysfunction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Ovarian dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Metabolic dysfunction-associated steatotic liver disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Metabolic dysfunction-associated steatotic liver disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Metabolic dysfunction-associated steatohepatitis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Metabolic dysfunction-associated steatohepatitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Sexual dysfunction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Sexual dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Phagocyte bactericidal dysfunction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Phagocyte bactericidal dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Bowel dysfunction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Bowel dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Labyrinthine dysfunction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Labyrinthine dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
arthrogryposis, renal dysfunction, and cholestasis 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease arthrogryposis, renal dysfunction, and cholestasis 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vertebral anomalies and variable endocrine and T-cell dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
arthrogryposis, renal dysfunction, and cholestasis 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease arthrogryposis, renal dysfunction, and cholestasis 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Thiamine metabolism dysfunction syndrome 2 Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Thiamine metabolism dysfunction syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Surfactant metabolism dysfunction Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Surfactant metabolism dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Multisystemic smooth muscle dysfunction syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Multisystemic smooth muscle dysfunction syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Sinoatrial node dysfunction and deafness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Sinoatrial node dysfunction and deafness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Cerebellar dysfunction Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Pulmonary Surfactant Metabolism Dysfunction Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Pulmonary Surfactant Metabolism Dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Diastolic dysfunction Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Diastolic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Thiamine Metabolism Dysfunction Syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Thiamine Metabolism Dysfunction Syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Vertebral anomalies and variable endocrine and T-cell dysfunction Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Vertebral anomalies and variable endocrine and T-cell dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Exploratory eye movement dysfunction in schizophrenia (responsive search score) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Exploratory eye movement dysfunction in schizophrenia (responsive search score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Exploratory eye movement dysfunction in schizophrenia (number of eye fixations) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Exploratory eye movement dysfunction in schizophrenia (number of eye fixations) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Exploratory eye movement dysfunction in schizophrenia (cognitive search score) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Exploratory eye movement dysfunction in schizophrenia (cognitive search score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Memory dysfunction in frontotemporal lobe dementia Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Memory dysfunction in frontotemporal lobe dementia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Erectile dysfunction Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Erectile dysfunction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Erectile dysfunction and prostate cancer treatment Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Erectile dysfunction and prostate cancer treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Sexual dysfunction (SSRI/SNRI-related) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sexual dysfunction (SSRI/SNRI-related) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Sexual dysfunction (female) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Sexual dysfunction (female) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Erectile dysfunction in type 1 diabetes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Erectile dysfunction in type 1 diabetes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Carbonic anhydrase va deficiency, hyperammonemia due to Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Carbonic anhydrase va deficiency, hyperammonemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
SCID due to ADA deficiency, delayed onset Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the SCID due to ADA deficiency, delayed onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thrombophilia due to protein S deficiency, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thrombophilia due to protein S deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Severe combined immunodeficiency due to ADA deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Severe combined immunodeficiency due to ADA deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
HNSHA due to aldolase A deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the HNSHA due to aldolase A deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thrombophilia, hereditary, due to protein C deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Ehlers-Danlos-like syndrome due to tenascin-X deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Ehlers-Danlos-like syndrome due to tenascin-X deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Gaucher disease, atypical, due to saposin C deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Gaucher disease, atypical, due to saposin C deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Disordered steroidogenesis due to cytochrome p450 oxidoreductase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Disordered steroidogenesis due to cytochrome p450 oxidoreductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Megaloblastic anemia due to inborn errors of metabolism Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Megaloblastic anemia due to inborn errors of metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hemolytic anemia due to hexokinase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hemolytic anemia due to hexokinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Leigh syndrome due to mitochondrial complex I deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Leigh syndrome due to mitochondrial complex I deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Homocysteinemia due to MTHFR deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Homocysteinemia due to MTHFR deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Immunodeficiency due to ficolin 3 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Immunodeficiency due to ficolin 3 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thrombophilia due to activated protein C resistance Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thrombophilia due to activated protein C resistance phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hypermethioninemia due to adenosine kinase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hypermethioninemia due to adenosine kinase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Pseudohermaphroditism, female, with hypokalemia, due to glucocorticoid resistance Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Pseudohermaphroditism, female, with hypokalemia, due to glucocorticoid resistance phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thrombophilia due to thrombomodulin defect Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thrombophilia due to thrombomodulin defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Muscular dystrophy, congenital, due to ITGA7 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Muscular dystrophy, congenital, due to ITGA7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Immunodeficiency due to defect in cd3-zeta Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Immunodeficiency due to defect in cd3-zeta phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Homocystinuria due to MTHFR deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Homocystinuria due to MTHFR deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Leigh syndrome due to mitochondrial complex II deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Leigh syndrome due to mitochondrial complex II deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Complement component 4, partial deficiency of, due to dysfunctional c1 inhibitor Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Complement component 4, partial deficiency of, due to dysfunctional c1 inhibitor phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital muscular dystrophy due to partial LAMA2 deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital muscular dystrophy due to partial LAMA2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Megaloblastic anemia due to dihydrofolate reductase deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Megaloblastic anemia due to dihydrofolate reductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Obesity, severe, due to leptin deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Obesity, severe, due to leptin deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Adenylate kinase deficiency, hemolytic anemia due to Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Adenylate kinase deficiency, hemolytic anemia due to phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Thrombophilia, hereditary, due to protein C deficiency, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thrombophilia, hereditary, due to protein C deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Hyperphenylalaninemia, bh4-deficient, a, due to partial pts deficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Hyperphenylalaninemia, bh4-deficient, a, due to partial pts deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Congenital adrenal hyperplasia due to 21 hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset. |
Thrombophilia, X-Linked, Due To Factor Ix Defect Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Thrombophilia, X-Linked, Due To Factor Ix Defect from the curated CTD Gene-Disease Associations dataset. |
HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset. |
Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency from the curated CTD Gene-Disease Associations dataset. |
Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type from the curated CTD Gene-Disease Associations dataset. |
Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia due to from the curated CTD Gene-Disease Associations dataset. |
Congenital thrombotic disease, due to Protein C deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Congenital thrombotic disease, due to Protein C deficiency from the curated CTD Gene-Disease Associations dataset. |
ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO from the curated CTD Gene-Disease Associations dataset. |
Adenylate Kinase Deficiency, Hemolytic Anemia Due To Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Adenylate Kinase Deficiency, Hemolytic Anemia Due To from the curated CTD Gene-Disease Associations dataset. |
Neurodegeneration Due To Cerebral Folate Transport Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neurodegeneration Due To Cerebral Folate Transport Deficiency from the curated CTD Gene-Disease Associations dataset. |
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset. |
Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency from the curated CTD Gene-Disease Associations dataset. |
Severe combined immunodeficiency due to adenosine deaminase deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Severe combined immunodeficiency due to adenosine deaminase deficiency from the curated CTD Gene-Disease Associations dataset. |
Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency from the curated CTD Gene-Disease Associations dataset. |
Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to from the curated CTD Gene-Disease Associations dataset. |
METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT from the curated CTD Gene-Disease Associations dataset. |
Pseudohyperkalemia, Familial, 2, due to Red Cell Leak Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Pseudohyperkalemia, Familial, 2, due to Red Cell Leak from the curated CTD Gene-Disease Associations dataset. |
Krabbe Disease, Atypical, due to Saposin A Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Krabbe Disease, Atypical, due to Saposin A Deficiency from the curated CTD Gene-Disease Associations dataset. |
HEPATIC FIBROSIS, SEVERE, SUSCEPTIBILITY TO, DUE TO SCHISTOSOMA MANSONI INFECTION Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HEPATIC FIBROSIS, SEVERE, SUSCEPTIBILITY TO, DUE TO SCHISTOSOMA MANSONI INFECTION from the curated CTD Gene-Disease Associations dataset. |
Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency from the curated CTD Gene-Disease Associations dataset. |
Gaucher Disease, Atypical, Due To Saposin C Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Gaucher Disease, Atypical, Due To Saposin C Deficiency from the curated CTD Gene-Disease Associations dataset. |
Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to from the curated CTD Gene-Disease Associations dataset. |
Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Encephalopathy, Neonatal Severe, Due To Mecp2 Mutations from the curated CTD Gene-Disease Associations dataset. |
Thrombophilia Due To Elevated Histidine-Rich Glycoprotein Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Thrombophilia Due To Elevated Histidine-Rich Glycoprotein from the curated CTD Gene-Disease Associations dataset. |
Thrombophilia due to Activated Protein C Resistance Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Thrombophilia due to Activated Protein C Resistance from the curated CTD Gene-Disease Associations dataset. |
THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset. |
Immunodeficiency due to Defect in CD3-Zeta Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Immunodeficiency due to Defect in CD3-Zeta from the curated CTD Gene-Disease Associations dataset. |
Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset. |
Metachromatic Leukodystrophy due to Saposin B Deficiency Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Metachromatic Leukodystrophy due to Saposin B Deficiency from the curated CTD Gene-Disease Associations dataset. |
Immunodeficiency due to Defect in MAPBP-Interacting Protein Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Immunodeficiency due to Defect in MAPBP-Interacting Protein from the curated CTD Gene-Disease Associations dataset. |
HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO HEXOKINASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset. |
thrombocytopenia due to platelet alloimmunization Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease thrombocytopenia due to platelet alloimmunization in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
pneumoconiosis due to talc Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease pneumoconiosis due to talc in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hereditary spastic paraparesis due to a frame shift mutat Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hereditary spastic paraparesis due to a frame shift mutat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
depressed suicide; suicide due to depression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease depressed suicide; suicide due to depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
due Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term due in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
anemia due to reduced life span of red cells Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the anemia due to reduced life span of red cells phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
decreased cervical spine flexion due to contractures of posterior cervical muscles Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased cervical spine flexion due to contractures of posterior cervical muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
anemia due to reduced life span of red cells Gene SetFrom HPO Gene-Disease Associations genes associated with the anemia due to reduced life span of red cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
restricted neck movement due to contractures Gene SetFrom HPO Gene-Disease Associations genes associated with the restricted neck movement due to contractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
chronic rhinitis due to narrow nasal airway Gene SetFrom HPO Gene-Disease Associations genes associated with the chronic rhinitis due to narrow nasal airway phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
osteomyelitis due to immunodeficiency Gene SetFrom HPO Gene-Disease Associations genes associated with the osteomyelitis due to immunodeficiency 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 SetFrom 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. |
bowing of limbs due to multiple fractures Gene SetFrom HPO Gene-Disease Associations genes associated with the bowing of limbs due to multiple fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
osteomyelitis leading to amputation due to slow healing fractures Gene SetFrom HPO Gene-Disease Associations genes associated with the osteomyelitis leading to amputation due to slow healing fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
self-mutilation of tongue and lips due to involuntary movements Gene SetFrom HPO Gene-Disease Associations genes associated with the self-mutilation of tongue and lips due to involuntary movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
respiratory insufficiency due to defective ciliary clearance Gene SetFrom HPO Gene-Disease Associations genes associated with the respiratory insufficiency due to defective ciliary clearance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
recurrent infections due to aspiration Gene SetFrom HPO Gene-Disease Associations genes associated with the recurrent infections due to aspiration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
generalized hypotonia due to defect at the neuromuscular junction Gene SetFrom HPO Gene-Disease Associations genes associated with the generalized hypotonia due to defect at the neuromuscular junction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
chronic hepatitis due to cryptospridium infection Gene SetFrom HPO Gene-Disease Associations genes associated with the chronic hepatitis due to cryptospridium infection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
subperiosteal erosions due to secondary hyperparathyroidism Gene SetFrom HPO Gene-Disease Associations genes associated with the subperiosteal erosions due to secondary hyperparathyroidism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
painless fractures due to injury Gene SetFrom HPO Gene-Disease Associations genes associated with the painless fractures due to injury phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hepatic abscesses due to immunodeficiency Gene SetFrom HPO Gene-Disease Associations genes associated with the hepatic abscesses due to immunodeficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cellulitis due to immunodeficiency Gene SetFrom HPO Gene-Disease Associations genes associated with the cellulitis due to immunodeficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
{chronic infections, due to mbl deficiency} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {chronic infections, due to mbl deficiency} phenotype from the curated OMIM Gene-Disease Associations dataset. |
{hepatic fibrosis susceptibility due to schistosoma mansoni infection} Gene SetFrom OMIM Gene-Disease Associations genes associated with the {hepatic fibrosis susceptibility due to schistosoma mansoni infection} phenotype from the curated OMIM Gene-Disease Associations dataset. |
thrombophilia due to hrg deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the thrombophilia due to hrg deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
thrombophilia due to thrombomodulin defect Gene SetFrom OMIM Gene-Disease Associations genes associated with the thrombophilia due to thrombomodulin defect phenotype from the curated OMIM Gene-Disease Associations dataset. |
severe combined immunodeficiency due to il2 deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the severe combined immunodeficiency due to il2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
thrombophilia due to protein s deficiency, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the thrombophilia due to protein s deficiency, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
bleeding disorder due to p2rx1 defect Gene SetFrom OMIM Gene-Disease Associations genes associated with the bleeding disorder due to p2rx1 defect phenotype from the curated OMIM Gene-Disease Associations dataset. |
hemolytic anemia due to phosphofructokinase deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the hemolytic anemia due to phosphofructokinase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
nephropathy due to cfhr5 deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the nephropathy due to cfhr5 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
encephalopahty, lethal, due to defective mitochondrial peroxisomal fission Gene SetFrom OMIM Gene-Disease Associations genes associated with the encephalopahty, lethal, due to defective mitochondrial peroxisomal fission phenotype from the curated OMIM Gene-Disease Associations dataset. |
megaloblastic anemia due to dihydrofolate reductase deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the megaloblastic anemia due to dihydrofolate reductase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
thrombophilia due to protein s deficiency, autosomal dominant Gene SetFrom OMIM Gene-Disease Associations genes associated with the thrombophilia due to protein s deficiency, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset. |
chronic granulomatous disease, autosomal, due to deficiency of cyba Gene SetFrom OMIM Gene-Disease Associations genes associated with the chronic granulomatous disease, autosomal, due to deficiency of cyba phenotype from the curated OMIM Gene-Disease Associations dataset. |
?isolated growth hormone deficiency due to defect in ghrf Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?isolated growth hormone deficiency due to defect in ghrf phenotype from the curated OMIM Gene-Disease Associations dataset. |
thrombophilia due to heparin cofactor ii deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the thrombophilia due to heparin cofactor ii deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
obesity, morbid, due to leptin receptor deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the obesity, morbid, due to leptin receptor deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
hypercholesterolemia, due to ligand-defective apo b Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypercholesterolemia, due to ligand-defective apo b phenotype from the curated OMIM Gene-Disease Associations dataset. |
glucocorticoid deficiency, due to acth unresponsiveness Gene SetFrom OMIM Gene-Disease Associations genes associated with the glucocorticoid deficiency, due to acth unresponsiveness phenotype from the curated OMIM Gene-Disease Associations dataset. |
disordered steroidogenesis due to cytochrome p450 oxidoreductase Gene SetFrom OMIM Gene-Disease Associations genes associated with the disordered steroidogenesis due to cytochrome p450 oxidoreductase phenotype from the curated OMIM Gene-Disease Associations dataset. |
hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
muscular dystrophy, congenital, due to partial lama2 deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the muscular dystrophy, congenital, due to partial lama2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
hemorrhagic diathesis due to 'antithrombin' pittsburgh Gene SetFrom OMIM Gene-Disease Associations genes associated with the hemorrhagic diathesis due to 'antithrombin' pittsburgh phenotype from the curated OMIM Gene-Disease Associations dataset. |
immunodeficiency due to purine nucleoside phosphorylase deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the immunodeficiency due to purine nucleoside phosphorylase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
hemolytic anemia due to glutathione peroxidase deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the hemolytic anemia due to glutathione peroxidase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia Gene SetFrom OMIM Gene-Disease Associations genes associated with the hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset. |
thrombophilia due to protein c deficiency, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the thrombophilia due to protein c deficiency, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
lacticacidemia due to pdx1 deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the lacticacidemia due to pdx1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |