Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "G"

271 to 280 of 677 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
271	89944	GLB1L2	Galactosidase beta 1 like 2	MST114, MSTP114	Schizophrenia
272	112937	GLB1L3	Galactosidase beta 1 like 3	-	Alzheimer disease, Obesity
273	113263	GLCCI1	Glucocorticoid induced 1	FAM117C, GCTR, GIG18, TSSN1	Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Rotator cuff tear, Schizophrenia, Uterine fibroid
274	26035	GLCE	Glucuronic acid epimerase	HSEPI	Cerebrovascular disorder, Hypertension
275	2731	GLDC	Glycine decarboxylase	GCE, GCE1, GCSP, HYGN1	Asthma, Astrocytoma, Glycine encephalopathy, Generalized epilepsy, Global developmental delay, Hyperglycemia, Neurodevelopmental disorder, Obesity, Osteosarcoma, Retinitis pigmentosa
276	342035	GLDN	Gliomedin	CLOM, COLM, CRG-L2, CRGL2, LCCS11, UNC-112, UNC-122	Arthrogryposis multiplex congenita, Congenital deformity of clavicle, Congenital deformity of elbow, Congenital deformity of forearm, Congenital deformity of scapula, Congenital deformity of wrist, Congenital dislocation of elbow, Congenital glenohumeral joint dislocation, Congenital joint contractures, Contracture of multiple joints, Fetal akinesia deformation sequence, Lethal congenital contracture syndrome, Pena-shokeir syndrome , Pericarditis, Primary aldosteronism, Urinary bladder cancer View all (1 more)
277	2733	GLE1	GLE1 RNA export mediator	CAAHC, CAAHD, GLE1L, LCCS, LCCS1, hGLE1	Amyotrophic lateral sclerosis, Arthrogryposis with anterior horn cell disease, Congenital arthrogryposis with anterior horn cell disease, Hypertension, Lethal congenital contracture syndrome, Oligodendroglioma
278	2734	GLG1	Golgi glycoprotein 1	CFR-1, ESL-1, MG-160, MG160	Amyotrophic lateral sclerosis, Celiac disease, Color vision deficiency, Schizophrenia
279	2735	GLI1	GLI family zinc finger 1	GLI, PAPA8, PPD1	Bardet-biedl syndrome, Hepatocellular carcinoma, Ellis-van creveld syndrome, Gastrointestinal stromal tumor, Gout, Insomnia, Promyelocytic leukemia, Diffuse large b-cell lymphoma, Non-neoplastic peripheral nervous system disease, Premature ovarian failure, Peripheral nervous system disease, Peripheral neuropathy, Polydactyly, Postaxial polydactyly, Urinary bladder neoplasms
280	2736	GLI2	GLI family zinc finger 2	CJS, HPE9, PHS2, THP1, THP2	Alzheimer disease, Androgenetic alopecia, Cerebral arteriovenous malformations, Asthma, Bardet-biedl syndrome, Basal cell nevus syndrome, Bifid nose, Breast cancer, Basal cell carcinoma, Cleft face, Coloboma, Combined pituitary hormone deficiency, Congenital arteriovenous malformation, Craniosynostosis, Culler-jones syndrome View all (22 more)

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