Genes | GeDiPNet - Gene Disease Pathway & Associations

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2531 to 2540 of 12229 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
2531	161497	STRC	Stereocilin	DFNB16	Asthenozoospermia, Azoospermia, Deafness, Deafness-infertility syndrome, Hearing loss, Non-syndromic sensorineural deafness, Nonsyndromic deafness, Oligospermia, Sensorineural hearing loss, Spermatogenic failure
2532	1615	DARS1	Aspartyl-tRNA synthetase 1	DARS, HBSL, aspRS	Congenital microcephaly, Developmental regression, Diabetes mellitus, Hypomyelination with brainstem and spinal cord involvement and leg spasticity, Hypoplasia of corpus callosum, Leukodystrophy, Leukoencephalopathy, Lupus erythematosus, Motor delay, Nystagmus
2533	161502	CFAP161	Cilia and flagella associated protein 161	C15orf26	Prostate cancer
2534	161514	TBC1D21	TBC1 domain family member 21	MgcRabGAP	Exfoliation syndrome
2535	161582	DNAAF4	Dynein axonemal assembly factor 4	CILD25, DYX1, DYX1C1, DYXC1, EKN1, RD, pf23	Alexia, Asthenozoospermia, Asthma, Bronchiectasis, Chronic obstructive pulmonary disease, Ciliary dyskinesia, Asplenia, Congenital pectus excavatum, Corneal dystrophy, Developmental dyslexia, Dyslexia, Bronchitis, Hearing loss, Hydrocephalus, Kartagener syndrome View all (8 more)
2536	1616	DAXX	Death domain associated protein	BING2, DAP6, EAP1, SMIM40	Adrenocortical carcinoma, Anorexia, Bronchospasm, Glioblastoma, Heart failure, Iron deficiency anemia, Liver failure, Neuroendocrine tumor of stomach, Neuroendocrine tumors, Pancreatic endocrine carcinoma, Pancreatic neoplasm, Pancreatic cancer, Paraganglioma, Pulmonary carcinoid tumor, Rheumatoid arthritis View all (3 more)
2537	1617	DAZ1	Deleted in azoospermia 1	DAZ, SPGY	Azoospermia, Cryptorchidism, Non-obstructive azoospermia, Nonobstructive spermatogenic failure, y-linked, Oligospermia, Partial chromosome y deletion
2538	161725	OTUD7A	OTU deubiquitinase 7A	C15orf16, C16ORF15, CEZANNE2, NEDHS, OTUD7	Bipolar disorder, Heart failure, Mental depression, Schizophrenia
2539	161742	SPRED1	Sprouty related EVH1 domain containing 1	LGSS, NFLS, PPP1R147, hSpred1, spred-1	Anencephaly, Attention deficit hyperactivity disorder, Cafe-au-lait macules with pulmonary stenosis, Congenital epicanthus, Drachtman weinblatt sitarz syndrome, Dysmorphic features, High palate, Legius syndrome, Macrocephaly, Micrognathism, Multiple congenital anomalies, Multiple lipomata, Neurofibroma, Neurofibromatosis, Ptosis, Specific learning disorder View all (1 more)
2540	161779	PGBD4	PiggyBac transposable element derived 4	-	Mental depression

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