Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "G"

11 to 20 of 533 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
11	10243	GPHN	Gephyrin	GEPH, GPH, GPHRYN, HKPX1, MOCODC	Cerebellar hypoplasia, Cerebral atrophy, Combined molybdoflavoprotein enzyme deficiency, Congenital exomphalos, Developmental delay, Dyssomnia, Epileptic encephalopathy, Eosinophilia, Gastroesophageal reflux disease, Hereditary hyperekplexia, Hiatal hernia, Hyperekplexia, Mental depression, Mental retardation, Molybdenum cofactor deficiency View all (5 more)
12	10249	GLYAT	Glycine-N-acyltransferase	ACGNAT, CAT, GAT	Ankylosing spondylitis, Bipolar disorder, Cardiovascular diseases, Cholangitis, Crohn disease, Inflammatory bowel disease, Psoriasis, Ulcerative colitis
13	10457	GPNMB	Glycoprotein nmb	HGFIN, NMB, PLCA3	Amyloidosis, Amyloidosis cutis dyschromia, Breast cancer, Mammary neoplasms, Breast carcinoma, Colorectal cancer, Colorectal neoplasms, Endometriosis, Kidney failure, Liver failure, Marfan syndrome, Parkinson disease, Acute kidney insufficiency
14	105372419	GEMIN7-AS1	GEMIN7 antisense RNA 1	-	Alzheimer disease
15	105375382	GRM3-AS1	GRM3 antisense RNA 1	-	Development disorder, Schizophrenia
16	10634	GAS2L1	Growth arrest specific 2 like 1	GAR22	Leukemia, Myeloid leukemia
17	10672	GNA13	G protein subunit alpha 13	G13, HG1N	African burkitt`s lymphoma, Burkitt`s lymphoma, Diffuse lymphoma
18	10681	GNB5	G protein subunit beta 5	GB5, HG2E, IDDCA, LADCI, LDMLS1, LDMLS2, gbeta5	Attention deficit hyperactivity disorder, Colorectal cancer, Colorectal neoplasms, Developmental delay, Intellectual developmental disorder with cardiac arrhythmia, Intellectual disability-cardiac arrhythmia syndrome, Language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia, Mental retardation, Nystagmus, Sick sinus syndrome
19	10750	GRAP	GRB2 related adaptor protein	DFNB114	Hearing loss, Non-syndromic sensorineural deafness
20	10804	GJB6	Gap junction protein beta 6	CX30, DFNA3, DFNA3B, DFNB1B, ECTD2, ED2, EDH, HED, HED2	Alopecia, Aplasia cutis congenita, Arthritis, Cataract, Cerebellar hypoplasia, Conjunctivitis, Corneal erosion, Corneal neovascularization, Cryptorchidism, Deafness, Deafness, digenic, Dwarfism, Ectodermal dysplasia, Hearing loss, Hemiplegia/hemiparesis View all (26 more)

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