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 ▲ |
---|---|---|---|---|---|
C0023492 | Leukemia, T-Cell | SACM1L | 22908 | SAC1 like phosphatidylinositide phosphatase | Q9NTJ5 |
C0011847 | Diabetes | SACM1L | 22908 | SAC1 like phosphatidylinositide phosphatase | Q9NTJ5 |
C0007282 | Carotid Stenosis | SACM1L | 22908 | SAC1 like phosphatidylinositide phosphatase | Q9NTJ5 |
C0006142 | Malignant neoplasm of breast | SACM1L | 22908 | SAC1 like phosphatidylinositide phosphatase | Q9NTJ5 |
C1961102 | Precursor Cell Lymphoblastic Leukemia Lymphoma | SACM1L | 22908 | SAC1 like phosphatidylinositide phosphatase | Q9NTJ5 |
C0234533 | Generalized seizures | SACM1L | 22908 | SAC1 like phosphatidylinositide phosphatase | Q9NTJ5 |
C0003873 | Rheumatoid Arthritis | SACM1L | 22908 | SAC1 like phosphatidylinositide phosphatase | Q9NTJ5 |
C0342276 | Maturity onset diabetes mellitus in young | SACM1L | 22908 | SAC1 like phosphatidylinositide phosphatase | Q9NTJ5 |
C0011849 | Diabetes Mellitus | SACM1L | 22908 | SAC1 like phosphatidylinositide phosphatase | Q9NTJ5 |
C0751955 | Brain Infarction | SACM1L | 22908 | SAC1 like phosphatidylinositide phosphatase | Q9NTJ5 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | SACM1L | 22908 | SAC1 like phosphatidylinositide phosphatase | Q9NTJ5 |
C0020538 | Hypertensive disease | SACM1L | 22908 | SAC1 like phosphatidylinositide phosphatase | Q9NTJ5 |
C1956346 | Coronary Artery Disease | SACM1L | 22908 | SAC1 like phosphatidylinositide phosphatase | Q9NTJ5 |
C0029422 | Osteochondrodysplasias | SLC35D1 | 23169 | solute carrier family 35 member D1 | Q9NTN3 |
C0024236 | Lymphedema | SLC35D1 | 23169 | solute carrier family 35 member D1 | Q9NTN3 |
C0008925 | Cleft Palate | SLC35D1 | 23169 | solute carrier family 35 member D1 | Q9NTN3 |
C0020224 | Polyhydramnios | SLC35D1 | 23169 | solute carrier family 35 member D1 | Q9NTN3 |
C0432194 | Schneckenbecken dysplasia | SLC35D1 | 23169 | solute carrier family 35 member D1 | Q9NTN3 |
C0010417 | Cryptorchidism | SLC35D1 | 23169 | solute carrier family 35 member D1 | Q9NTN3 |
C0265282 | Fibrochondrogenesis | SLC35D1 | 23169 | solute carrier family 35 member D1 | Q9NTN3 |
C0013595 | Eczema | SLC35D1 | 23169 | solute carrier family 35 member D1 | Q9NTN3 |
C4721610 | Carcinoma, Ovarian Epithelial | ECHDC1 | 55862 | ethylmalonyl-CoA decarboxylase 1 | Q9NTX5 |
C1140680 | Malignant neoplasm of ovary | ECHDC1 | 55862 | ethylmalonyl-CoA decarboxylase 1 | Q9NTX5 |
C0699885 | Carcinoma of bladder | ECHDC1 | 55862 | ethylmalonyl-CoA decarboxylase 1 | Q9NTX5 |
C0005684 | Malignant neoplasm of urinary bladder | ECHDC1 | 55862 | ethylmalonyl-CoA decarboxylase 1 | Q9NTX5 |
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Last updated: August 19, 2024