Genes | GeDiPNet - Gene Disease Pathway & Associations

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1511 to 1520 of 12229 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1511	113189	CHST14	Carbohydrate sulfotransferase 14	ATCS, D4ST1, EDSMC1, HNK1ST	Adducted thumbs syndrome, Arachnodactyly, Arthrogryposis multiplex congenita, Atrial septal defect, Brachycephaly, Congenital clubfoot, Congenital exomphalos, Congenital malrotation of intestine, Congenital pectus excavatum, Cryptorchidism, Developmental delay, Distal arthrogryposis, Musculocontractural ehlers-danlos syndrome, Glaucoma, Hiatal hernia View all (15 more)
1512	1132	CHRM4	Cholinergic receptor muscarinic 4	HM4, M4R	Catatonia, Malignant catatonia, Schizophrenia
1513	11320	MGAT4A	Alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase A	GNT-IV, GNT-IVA, GnT-4a	Bipolar disorder, Colorectal neoplasms, Hypoplastic left heart syndrome
1514	11321	GPN1	GPN-loop GTPase 1	ATPBD1A, MBDIN, NTPBP, RPAP4, XAB1	Gout, Gouty arthritis, Malignant neoplasm of anterior portion of floor of mouth, Malignant neoplasm of lip and oral cavity, Malignant neoplasm of mouth, Malignant tumor of lateral floor of mouth, Metabolic syndrome, Mouth neoplasms, Malignant neoplasm of floor of mouth
1515	11322	TMC6	Transmembrane channel like 6	EV1, EVER1, EVIN1, LAK-4P, TNRC6C-AS1, lnc	Cafe-au-lait spot, Carcinoma, Epidermodysplasia verruciformis, Seborrheic dermatitis
1516	113220	KIF12	Kinesin family member 12	PFIC8	Coronary heart disease
1517	113235	SLC46A1	Solute carrier family 46 member 1	G21, HCP1, HsPCFT, PCFT, hPCFT	Anemia, Anorexia, Cheilitis, Congenital defect of folate absorption, Developmental delay, Dyskinetic syndrome, Eosinophilia, Gastroesophageal reflux disease, Glossitis, Hereditary folate malabsorption, Hyperhomocysteinemia, Immunologic deficiency syndromes, Leukopenia, Malabsorption syndrome, Mental retardation View all (4 more)
1518	113246	C12orf57	Chromosome 12 open reading frame 57	C10, GRCC10	Agenesis of corpus callosum, Aortic aneurysm, Aortic valve insufficiency, Atrophy of kidney, Attention deficit hyperactivity disorder, Brachydactyly, Camptodactyly of fingers, Congenital clubfoot, Congenital coloboma of iris, Developmental delay, Dolichocephaly, Epilepsy, Frontal bossing, Fundus coloboma, Hydronephrosis View all (10 more)
1519	113251	LARP4	La ribonucleoprotein 4	PP13296	Sclerocystic ovaries, Polycystic ovary syndrome
1520	11326	VSIG4	V-set and immunoglobulin domain containing 4	CRIg, Z39IG	Alopecia, Glomerulonephritis, Leukemia, Liver carcinoma, Myeloid leukemia

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