Genes | GeDiPNet - Gene Disease Pathway & Associations

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3511 to 3520 of 12229 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
3511	23225	NUP210	Nucleoporin 210	GP210, POM210	Coronary artery disease, Diabetes mellitus, Myocardial infarction
3512	23228	PLCL2	Phospholipase C like 2	PLCE2	Biliary cirrhosis, Mental depression, Mood disorder, Myocardial infarction, Psoriasis, Psoriasis vulgaris, Rheumatoid arthritis, Schizophrenia
3513	23229	ARHGEF9	Cdc42 guanine nucleotide exchange factor 9	COLLYBISTIN, DEE8, EIEE8, HPEM-2, PEM-2, PEM2	Alopecia, Developmental regression, Dyscognitive seizures, Epileptic encephalopathy, Hyperekplexia-epilepsy syndrome, Mental retardation, Seizure, Trigonocephaly
3514	23230	VPS13A	Vacuolar protein sorting 13 homolog A	BLTP5A, CHAC, CHOREIN	Abetalipoproteinemia, Anxiety disorder, Attention deficit hyperactivity disorder, Cataract, Cerebral cortical atrophy, Chorea, Choreoacanthocytosis, Colorectal cancer, Developmental regression, Distal muscular atrophy, Dwarfism, Dysarthria, Dysgraphia, Dysphagia, Dyssomnia View all (15 more)
3515	23233	EXOC6B	Exocyst complex component 6B	SEC15B, SEC15L2, SEMDJL3	Congenital clubfoot, Dislocated radial head, Cutis marmorata, Developmental delay, Dolichocephaly, Dwarfism, Dysmorphic features, Ectopia lentis, Eczema, Heart septal defects, High palate, Hirschsprung disease, Mental retardation, Micromelia, Movement disorders View all (8 more)
3516	23235	SIK2	Salt inducible kinase 2	LOH11CR1I, QIK, SIK-2, SNF1LK2	Asthma, Cholangitis, Sclerosing cholangitis
3517	23236	PLCB1	Phospholipase C beta 1	DEE12, EIEE12, PI-PLC, PLC-154, PLC-I, PLC-beta-1, PLC154, PLCB1A, PLCB1B	Bipolar disorder, Breast cancer, Cardiovascular diseases, Colonic neoplasms, Developmental regression, Epilepsy, Epileptic encephalopathy, Malignant migrating partial seizures of infancy, Mental depression, Myelodysplastic syndrome, Biliary cirrhosis, Schizophrenia, Seizure, Sleep apnea, Spasms syndrome, West syndrome View all (1 more)
3518	23237	ARC	Activity regulated cytoskeleton associated protein	Arg3.1, hArc	Alzheimer disease, Movement disorders, Schizophrenia, Senile dementia, Status marmoratus
3519	2324	FLT4	Fms related receptor tyrosine kinase 4	CHTD7, FLT-4, FLT41, LMPH1A, LMPHM1, PCL, VEGFR-3, VEGFR3	Capillary hemangioma, Congenital epicanthus, Dysmorphic features, Erysipelas, Hemangioma, Hemangiosarcoma, Hydrops fetalis, Hyperkeratosis, Hypoplasia of lymphatic vessels, Metastatic melanoma, Milroy disease, Multiple congenital anomalies, Sclerocystic ovaries, Polycystic ovary syndrome, Renal carcinoma View all (7 more)
3520	23240	TMEM131L	Transmembrane 131 like	KIAA0922	Narcolepsy

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