Genes | GeDiPNet - Gene Disease Pathway & Associations

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11861 to 11870 of 15380 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
11861	79729	SH3D21	SH3 domain containing 21	C1orf113	Diabetes mellitus type 2
11862	6455	SH3GL1	SH3 domain containing GRB2 like 1, endophilin A2	CNSA1, EEN, SH3D2B, SH3P8	Breast cancer, Hepatocellular carcinoma, Myeloid leukemia
11863	6456	SH3GL2	SH3 domain containing GRB2 like 2, endophilin A1	CNSA2, EEN-B1, SH3D2A, SH3P4	Osteonecrosis of the femoral head, Parkinson disease
11864	6457	SH3GL3	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
11865	30011	SH3KBP1	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
11866	9644	SH3PXD2A	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)
11867	285590	SH3PXD2B	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
11868	57630	SH3RF1	SH3 domain containing ring finger 1	POSH, RNF142, SH3MD2	Alzheimer disease, Cerebral amyloid angiopathy, Dementia, Eosinophilia, Major depressive disorder, Prostate cancer, Psychotic disorders, Schizophrenia
11869	344558	SH3RF3	SH3 domain containing ring finger 3	POSH2, SH3MD4	Alzheimer disease, Amphetamine or sympathomimetic abuse, Astrocytoma, Color vision deficiency, Dementia, Schizophrenia
11870	54436	SH3TC1	SH3 domain and tetratricopeptide repeats 1	-	Colorectal neoplasms

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