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 3101 - 3125 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0028738 Nystagmus ELOVL5 60481 ELOVL fatty acid elongase 5 Q9NYP7
C1319315 Adenocarcinoma of large intestine ELOVL5 60481 ELOVL fatty acid elongase 5 Q9NYP7
C3554460 COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 ELOVL5 60481 ELOVL fatty acid elongase 5 Q9NYP7
C0346629 Malignant neoplasm of large intestine ELOVL5 60481 ELOVL fatty acid elongase 5 Q9NYP7
C0339573 Glaucoma, Primary Open Angle ELOVL5 60481 ELOVL fatty acid elongase 5 Q9NYP7
C0018790 Cardiac Arrest ELOVL5 60481 ELOVL fatty acid elongase 5 Q9NYP7
C0015695 Fatty Liver ELOVL5 60481 ELOVL fatty acid elongase 5 Q9NYP7
C0011860 Diabetes Mellitus, Non-Insulin-Dependent ELOVL5 60481 ELOVL fatty acid elongase 5 Q9NYP7
C0600139 Prostate carcinoma ELOVL5 60481 ELOVL fatty acid elongase 5 Q9NYP7
C1269683 Major Depressive Disorder ELOVL5 60481 ELOVL fatty acid elongase 5 Q9NYP7
C1306459 Primary malignant neoplasm ELOVL5 60481 ELOVL fatty acid elongase 5 Q9NYP7
C0006826 Malignant Neoplasms ELOVL5 60481 ELOVL fatty acid elongase 5 Q9NYP7
C0752124 Spinocerebellar Ataxia Type 6 (disorder) ELOVL5 60481 ELOVL fatty acid elongase 5 Q9NYP7
C0752125 Spinocerebellar Ataxia Type 7 ELOVL5 60481 ELOVL fatty acid elongase 5 Q9NYP7
C2711227 Steatohepatitis ELOVL5 60481 ELOVL fatty acid elongase 5 Q9NYP7
C0752120 Spinocerebellar Ataxia Type 1 ELOVL5 60481 ELOVL fatty acid elongase 5 Q9NYP7
C0028754 Obesity ELOVL5 60481 ELOVL fatty acid elongase 5 Q9NYP7
C1864446 Retinitis Pigmentosa 25 ELOVL5 60481 ELOVL fatty acid elongase 5 Q9NYP7
C0752123 Spinocerebellar Ataxia Type 5 ELOVL5 60481 ELOVL fatty acid elongase 5 Q9NYP7
C0752121 Spinocerebellar Ataxia Type 2 ELOVL5 60481 ELOVL fatty acid elongase 5 Q9NYP7
C0752122 Spinocerebellar Ataxia Type 4 ELOVL5 60481 ELOVL fatty acid elongase 5 Q9NYP7
C0235782 Gallbladder Carcinoma CYP39A1 51302 cytochrome P450 family 39 subfamily A member 1 Q9NYL5
C0023530 Leukopenia CYP39A1 51302 cytochrome P450 family 39 subfamily A member 1 Q9NYL5
C0153452 Malignant neoplasm of gallbladder CYP39A1 51302 cytochrome P450 family 39 subfamily A member 1 Q9NYL5
C0037773 Spastic Paraplegia, Hereditary CYP39A1 51302 cytochrome P450 family 39 subfamily A member 1 Q9NYL5

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Last updated: August 19, 2024