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 40851 - 40875 of 62743 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Gene Name UniProt ID
C0027651 Neoplasms FDFT1 2222 farnesyl-diphosphate farnesyltransferase 1 P37268
C0342731 Deficiency of mevalonate kinase FDFT1 2222 farnesyl-diphosphate farnesyltransferase 1 P37268
C2239176 Liver carcinoma FDFT1 2222 farnesyl-diphosphate farnesyltransferase 1 P37268
C0398691 Hyperimmunoglobulinemia D FDFT1 2222 farnesyl-diphosphate farnesyltransferase 1 P37268
C0020473 Hyperlipidemia FDFT1 2222 farnesyl-diphosphate farnesyltransferase 1 P37268
C0006870 Cannabis Dependence FDFT1 2222 farnesyl-diphosphate farnesyltransferase 1 P37268
C0684249 Carcinoma of lung FDFT1 2222 farnesyl-diphosphate farnesyltransferase 1 P37268
C0025202 melanoma FDFT1 2222 farnesyl-diphosphate farnesyltransferase 1 P37268
C0006868 Cannabis Abuse FDFT1 2222 farnesyl-diphosphate farnesyltransferase 1 P37268
C2711227 Steatohepatitis FDFT1 2222 farnesyl-diphosphate farnesyltransferase 1 P37268
C0031391 Phencyclidine Abuse FDFT1 2222 farnesyl-diphosphate farnesyltransferase 1 P37268
C0011603 Dermatitis FDFT1 2222 farnesyl-diphosphate farnesyltransferase 1 P37268
C1959626 Mevalonic Aciduria FDFT1 2222 farnesyl-diphosphate farnesyltransferase 1 P37268
C3714756 Intellectual Disability FDFT1 2222 farnesyl-diphosphate farnesyltransferase 1 P37268
C0007222 Cardiovascular Diseases FDFT1 2222 farnesyl-diphosphate farnesyltransferase 1 P37268
C1621958 Glioblastoma Multiforme FDFT1 2222 farnesyl-diphosphate farnesyltransferase 1 P37268
C0376358 Malignant neoplasm of prostate FDFT1 2222 farnesyl-diphosphate farnesyltransferase 1 P37268
C0600427 Cocaine Dependence FDFT1 2222 farnesyl-diphosphate farnesyltransferase 1 P37268
C0001418 Adenocarcinoma FDFT1 2222 farnesyl-diphosphate farnesyltransferase 1 P37268
C0282102 Chondrodysplasia punctata, X-linked dominant type FDFT1 2222 farnesyl-diphosphate farnesyltransferase 1 P37268
C0038379 Strabismus FCSK 197258 fucose kinase Q8N0W3
C3714756 Intellectual Disability FCSK 197258 fucose kinase Q8N0W3
C0282577 Congenital Disorders of Glycosylation FCSK 197258 fucose kinase Q8N0W3
C0028738 Nystagmus FCSK 197258 fucose kinase Q8N0W3
C0036572 Seizures FCSK 197258 fucose kinase Q8N0W3

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Last updated: August 19, 2024