DisGeNET

DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.

Source Last Updated
DisGeNET July 29, 2024
Displaying entries 15326 - 15350 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▲ UniProt ID
C0080174 Spina Bifida Occulta B3GLCT 145173 beta 3-glucosyltransferase Q6Y288
C0010308 Congenital Hypothyroidism B3GLCT 145173 beta 3-glucosyltransferase Q6Y288
C0272137 Tn Syndrome B3GLCT 145173 beta 3-glucosyltransferase Q6Y288
C0266295 Congenital hypoplasia of kidney B3GLCT 145173 beta 3-glucosyltransferase Q6Y288
C0002871 Anemia B3GLCT 145173 beta 3-glucosyltransferase Q6Y288
C0003466 Anus, Imperforate B3GLCT 145173 beta 3-glucosyltransferase Q6Y288
C0086543 Cataract B3GLCT 145173 beta 3-glucosyltransferase Q6Y288
C1306503 Congenital exomphalos B3GLCT 145173 beta 3-glucosyltransferase Q6Y288
C0025958 Microcephaly B3GLCT 145173 beta 3-glucosyltransferase Q6Y288
C0221356 Brachycephaly B3GLCT 145173 beta 3-glucosyltransferase Q6Y288
C1862389 ATRIAL SEPTAL DEFECT 1 B3GLCT 145173 beta 3-glucosyltransferase Q6Y288
C0018816 Heart Septal Defects B3GLCT 145173 beta 3-glucosyltransferase Q6Y288
C3665347 Visual Impairment B3GLCT 145173 beta 3-glucosyltransferase Q6Y288
C3887608 HYDROCEPHALUS, NONSYNDROMIC, AUTOSOMAL RECESSIVE 1 B3GLCT 145173 beta 3-glucosyltransferase Q6Y288
C0039075 Syndactyly B3GLCT 145173 beta 3-glucosyltransferase Q6Y288
C0848558 Hypospadias B3GLCT 145173 beta 3-glucosyltransferase Q6Y288
C0020295 Hydronephrosis B3GLCT 145173 beta 3-glucosyltransferase Q6Y288
C0019294 Hernia, Inguinal B3GLCT 145173 beta 3-glucosyltransferase Q6Y288
C0265259 Popliteal pterygium syndrome B3GLCT 145173 beta 3-glucosyltransferase Q6Y288
C0017601 Glaucoma B3GLCT 145173 beta 3-glucosyltransferase Q6Y288
C3714581 Multicystic Dysplastic Kidney B3GLCT 145173 beta 3-glucosyltransferase Q6Y288
C0005745 Blepharoptosis B3GLCT 145173 beta 3-glucosyltransferase Q6Y288
C0036439 Scoliosis, unspecified B3GLCT 145173 beta 3-glucosyltransferase Q6Y288
C0152101 Hypoplastic Left Heart Syndrome B3GLCT 145173 beta 3-glucosyltransferase Q6Y288
C0027092 Myopia B3GLCT 145173 beta 3-glucosyltransferase Q6Y288

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Last updated: August 19, 2024