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 |
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DisGeNET | July 29, 2024 |
Disease ID | Disease Name | Gene Symbol | Gene ID ▲ | Gene Name | UniProt ID |
---|---|---|---|---|---|
C0848558 | Hypospadias | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0036631 | Seminoma | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0852036 | Pregnancy associated hypertension | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0011581 | Depressive disorder | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0497327 | Dementia | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0242342 | Sheehan Syndrome | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0750887 | Adrenal Cancer | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0034013 | Precocious Puberty | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0001622 | Adrenal Gland Hyperfunction | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0022658 | Kidney Diseases | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0005974 | Bone Resorption | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0007113 | Rectal Carcinoma | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0700095 | Central neuroblastoma | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C1134719 | Invasive Ductal Breast Carcinoma | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0858252 | Breast adenocarcinoma | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0013336 | Dwarfism | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C1956346 | Coronary Artery Disease | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C3642346 | Luminal B Breast Carcinoma | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0152013 | Adenocarcinoma of lung (disorder) | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0014859 | Esophageal Neoplasms | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0010054 | Coronary Arteriosclerosis | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0520463 | Chronic active hepatitis | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0400966 | Non-alcoholic Fatty Liver Disease | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0302592 | Cervix carcinoma | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
C0033804 | Pseudohermaphroditism | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
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Last updated: August 19, 2024