Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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11921 to 11930 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

11921
SH3 domain containing GRB2 like 3, endophilin A3
CNSA3, EEN-B2, HsT19371, SH3D2C, SH3P13
Kidney disease, Obstructive pulmonary disease, Developmental dysplasia of the hip, Female infertility, Inflammatory bowel disease, Schizophrenia, Uterine fibroid

11922
SH3 domain containing kinase binding protein 1
AGMX2, CD2BP3, CIN85, GIG10, HSB-1, HSB1, IMD61, MIG18
Colonic neoplasms, Immunodeficiency, X-linked common variable immunodeficiency phenotype due to sh3kbp1 deficiency

11923
SH3 and PX domains 2A
FISH, SH3MD1, TKS5
Asthma, Atrial fibrillation, Atrioventricular block, Cardiac arrhythmia, Cardioembolic stroke, Cerebrovascular disorder, Obstructive pulmonary disease, Diverticular disease, Hypertension, Iga nephropathy, Major depressive disorder, Malignant peripheral nerve sheath tumor, Malignant triton tumor, Potassium deficiency, Rheumatoid arthritis
View all (5 more)

11924
SH3 and PX domains 2B
FAD49, FTHS, HOFI, KIAA1295, TKS4, TSK4
Androgenetic alopecia, Bone disease, Craniofacial abnormalities, Desbuquois syndrome, Eye abnormalities, Glaucoma, Growth disorder, Hearing loss, Ocular hypertension, Oligodendroglioma, Preeclampsia, Prostate cancer

11925
SH3 domain containing ring finger 1
POSH, RNF142, SH3MD2
Alzheimer disease, Cerebral amyloid angiopathy, Dementia, Eosinophilia, Major depressive disorder, Prostate cancer, Psychotic disorders, Schizophrenia

11926
SH3 domain containing ring finger 3
POSH2, SH3MD4
Alzheimer disease, Amphetamine or sympathomimetic abuse, Astrocytoma, Color vision deficiency, Dementia, Schizophrenia

11927
SH3 domain and tetratricopeptide repeats 1
-
Colorectal neoplasms

11928
SH3 domain and tetratricopeptide repeats 2
CMT4C, MNMN
Arthrogryposis multiplex congenita, Breast cancer, Charcot-marie-tooth disease, Congenital hemihypertrophy, Congenital joint contractures, Congenital pes cavus, Dejerine-sottas disease, Distal spinal muscular atrophy, Hereditary motor and sensory neuropathies, Motor neuron disease, Hypertension, Hypertrophic neuropathy, Peripheral neuropathy, Peroneal muscle atrophy, Psoriasis
View all (4 more)

11929
SH3 and SYLF domain containing 1
RAY
Large artery stroke, Metabolic syndrome, Willis-ekbom disease, Diabetes mellitus type 2

11930
SH3 and multiple ankyrin repeat domains 1
SPANK-1, SSTRIP, synamon
Anxiety disorder, Autism, Breast cancer, Renal cell carcinoma, Neurodevelopmental disorder, Developmental coordination disorder, Insomnia, Intellectual developmental disorder, Motor skills disorder, Non-organic psychosis, Non-specific syndromic intellectual disability, Psychotic disorders, Schizophrenia