Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "G"

371 to 380 of 533 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
371	399972	GSEC	G-quadruplex forming sequence containing lncRNA	DCPS-AS1, ST3GAL4-AS1	Al-raqad syndrome
372	404672	GTF2H5	General transcription factor IIH subunit 5	C6orf175, TFB5, TFIIH, TGF2H5, TTD, TTD-A, TTD3, TTDA, bA120J8.2	Anemia, Asthma, Astigmatism, Bronchospasm, Carcinoma, Cardiomyopathy, Cataract, Cerebral cortical atrophy, Congenital epicanthus, Congenital exfoliative erythroderma, Congenital exomphalos, Congenital nonbullous ichthyosiform erythroderma, Craniosynostosis, Cryptorchidism, Dental enamel hypoplasia View all (30 more)
373	440435	GPR179	G protein-coupled receptor 179	CSNB1E, GPR158L, GPR158L1	Congenital stationary night blindness, Disorder of eye, Hypoplasia of optic disc, Myopia, Night blindness, Nyctalopia, Nystagmus, Strabismus, Congenital stationary night blindness, x-linked
374	449520	GGNBP1	Gametogenetin binding protein 1 (pseudogene)	-	Development disorder, Hodgkin disease, Lymphocytic leukemia, Malignant testicular germ cell tumor, Multiple myeloma, Multiple sclerosis, Nasopharyngeal carcinoma, Schizophrenia, Testicular neoplasms, Testicular germ cell tumor
375	4616	GADD45B	Growth arrest and DNA damage inducible beta	GADD45BETA, MYD118	Arsenic encephalopathy, Dermatologic disorders, Nonorganic psychosis, Psychosis
376	474344	GIMAP6	GTPase, IMAP family member 6	IAN-2, IAN-6, IAN2, IAN6	Oral ulcer
377	4935	GPR143	G protein-coupled receptor 143	NYS6, OA1	Albinism, Astigmatism, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Disorder of eye, Horizontal nystagmus, Hyperopic astigmatism, Myopia, Nystagmus, Nystagmus, congenital, x-linked, Nystagmus-induced head nodding, Ocular albinism, Ocular albinism, x-linked, Skin neoplasms, Strabismus View all (1 more)
378	50486	G0S2	G0/G1 switch 2	-	Anaplastic carcinoma, Carcinoma
379	50628	GEMIN4	Gem nuclear organelle associated protein 4	HC56, HCAP1, HHRF-1, NEDMCR, p97	Cataract, Congenital cataract, Developmental dysplasia of the hip, Developmental delay, Dysphagia, Gastroesophageal reflux disease, High palate, Hydronephrosis, Microcephaly, Micrognathism, Neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities, Osteopenia, Renal hypoplasia
380	51053	GMNN	Geminin DNA replication inhibitor	Gem, MGORS6	Camptodactyly of fingers, Breast aplasia, Anotia, Mandibular aplasia, Congenital exomphalos, Congenital hypoplasia of penis, Craniosynostosis, Cryptorchidism, Developmental delay, Dwarfism, Ear diseases, Ear-patella-short stature syndrome, Entropion, Epispadias, Frontal bossing View all (27 more)

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