Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "Y"

11 to 20 of 26 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
11	4904	YBX1	Y-box binding protein 1	BP-8, CBF-A, CSDA2, CSDB, DBPB, EFI-A, MDR-NF1, NSEP-1, NSEP1, YB-1, YB1	Breast cancer, Mammary neoplasms, Breast carcinoma, Colonic neoplasms, Marfan syndrome
12	51067	YARS2	Tyrosyl-tRNA synthetase 2	CGI-04, MLASA2, MT-TYRRS, TYRRS	Amyotrophy, Anemia, Bilateral convulsive seizures, Cerebellar atrophy, Dysphagia, Encephalopathy, Glaucoma, High palate, Limb muscle atrophy, Mental retardation, Microcephaly, Micrognathism, Mitochondrial diseases, Mitochondrial myopathy, Mitochondrial myopathy and sideroblastic anemia View all (10 more)
13	51441	YTHDF2	YTH N6-methyladenosine RNA binding protein F2	CAHL, DF2, HGRG8, NY-REN-2	Liver carcinoma
14	55249	YY1AP1	YY1 associated protein 1	GRNG, HCCA1, HCCA2, YY1AP	Aortic valve insufficiency, Brachydactyly, Carotid artery stenosis, Clinodactyly, Grange syndrome, Hypertension, Mental retardation, Patent ductus arteriosus, Renal artery stenosis, Specific learning disorder, Syndactyly, Ventricular septal defect
15	55689	YEATS2	YEATS domain containing 2	FAME4	Autism, Benign myoclonic epilepsy
16	56252	YLPM1	YLP motif containing 1	C14orf170, PPP1R169, ZAP113, ZAP3	Leukemia, Mental depression, Mood disorder
17	64848	YTHDC2	YTH N6-methyladenosine RNA binding protein C2	CAHL, hYTHDC2	Diabetes mellitus
18	7525	YES1	YES proto-oncogene 1, Src family tyrosine kinase	HsT441, P61-YES, Yes, c-yes	Cardiovascular diseases, Double outlet right ventricle, Hypertension, Taussig-bing anomaly, Ventricular septal defect
19	7528	YY1	YY1 transcription factor	DELTA, GADEVS, INO80S, NF-E1, UCRBP, YIN-YANG-1	Benign neoplasm, Uterine cervix neoplasm, Cervical cancer, Colorectal neoplasms, Cryptorchidism, Developmental delay, Gabriele de vries syndrome, Mental retardation, Malignant neoplasm, Neoplasms, Posteriorly rotated ear, Strabismus
20	7531	YWHAE	Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon	14-3-3E, HEL2, KCIP-1, MDCR, MDS	17p13.3 duplication syndrome, Bipolar disorder, Camptodactyly of fingers, Cardiovascular abnormalities, Cerebral cortical atrophy, Developmental dysplasia of the hip, Congenital epicanthus, Congenital hypoplasia of penis, Congenital omphalocele, Developmental delay, Distal 17p13.3 microdeletion syndrome, Endometrial stromal sarcoma, Frontal bossing, High palate, Hypoplasia of corpus callosum View all (6 more)

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