Genes | GeDiPNet - Gene Disease Pathway & Associations

Dataset:

All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

1531 to 1540 of 12229 Genes

Show

	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1531	11342	RNF13	Ring finger protein 13	DEE73, EIEE73, RZF	Cataract, Central visual impairment, Congenital microcephaly, Developmental delay, Epileptic encephalopathy, Hearing loss, Hypoplasia of corpus callosum, Mental retardation, Microcephaly, Myocardial infarction, Scoliosis, Visual cortex disease
1532	11343	MGLL	Monoglyceride lipase	HU-K5, HUK5, MAGL, MGL	Diabetes mellitus, Metabolic syndrome, Osteoporosis
1533	11344	TWF2	Twinfilin actin binding protein 2	A6RP, A6r, MSTP011, PTK9L	Anxiety disorder, Development disorder, Schizophrenia
1534	113444	SMIM12	Small integral membrane protein 12	C1orf212	Deafness, Deafness, digenic, Erythrokeratodermia variabilis, Erythrokeratodermia variabilis et progressiva, Nonsyndromic deafness
1535	113457	TUBA3D	Tubulin alpha 3d	H2-ALPHA, KTCN9, TUBA2	Keratoconus
1536	11346	SYNPO	Synaptopodin	SYNPO1	Focal segmental glomerulosclerosis, Glomerulosclerosis
1537	1135	CHRNA2	Cholinergic receptor nicotinic alpha 2 subunit	-	Alzheimer disease, Asthma, Benign seizures, Bipolar disorder, Epilepsy, Lung neoplasms, Lung cancer, Mental depression, Nocturnal epilepsy, Schizophrenia
1538	113510	HELQ	Helicase, POLQ like	HEL308	Breast cancer, Head and neck neoplasms
1539	113523636	SMIM40	Small integral membrane protein 40	-	Rheumatoid arthritis
1540	1136	CHRNA3	Cholinergic receptor nicotinic alpha 3 subunit	BAIPRCK, LNCR2, NACHRA3, PAOD2	Chronic obstructive pulmonary disease, Clonic seizures, Congenital anomalies of kidney and urinary tract, Coronary heart disease, Development disorder, Dysautonomia, Bronchitis, Hypotonic seizures, Jacksonian seizure, Lung neoplasms, Lung carcinoma, Lung adenocarcinoma, Lung cancer, Nasopharyngeal carcinoma, Schizophrenia, Seizure View all (1 more)

«««...152 153154155 156...»»»