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 |
Disease ID | Disease Name | Gene Symbol | Gene ID ▼ | Gene Name | UniProt ID |
---|---|---|---|---|---|
C0018801 | Heart failure | SPHK1 | 8877 | sphingosine kinase 1 | Q9NYA1 |
C0282160 | Aplasia Cutis Congenita | SPHK1 | 8877 | sphingosine kinase 1 | Q9NYA1 |
C0699885 | Carcinoma of bladder | SPHK1 | 8877 | sphingosine kinase 1 | Q9NYA1 |
C0600139 | Prostate carcinoma | SPHK1 | 8877 | sphingosine kinase 1 | Q9NYA1 |
C0040136 | Thyroid Neoplasm | SPHK1 | 8877 | sphingosine kinase 1 | Q9NYA1 |
C0004364 | Autoimmune Diseases | SPHK1 | 8877 | sphingosine kinase 1 | Q9NYA1 |
C0750952 | Biliary Tract Cancer | SPHK1 | 8877 | sphingosine kinase 1 | Q9NYA1 |
C0001430 | Adenoma | SPHK1 | 8877 | sphingosine kinase 1 | Q9NYA1 |
C0007847 | Malignant tumor of cervix | SPHK1 | 8877 | sphingosine kinase 1 | Q9NYA1 |
C0005695 | Bladder Neoplasm | SPHK1 | 8877 | sphingosine kinase 1 | Q9NYA1 |
C0033860 | Psoriasis | SPHK1 | 8877 | sphingosine kinase 1 | Q9NYA1 |
C0235782 | Gallbladder Carcinoma | SPHK1 | 8877 | sphingosine kinase 1 | Q9NYA1 |
C0079731 | B-Cell Lymphomas | SPHK1 | 8877 | sphingosine kinase 1 | Q9NYA1 |
C0235974 | Pancreatic carcinoma | SPHK1 | 8877 | sphingosine kinase 1 | Q9NYA1 |
C0033860 | Psoriasis | VNN1 | 8876 | vanin 1 | O95497 |
C0025517 | Metabolic Diseases | VNN1 | 8876 | vanin 1 | O95497 |
C0015624 | Fanconi Syndrome | VNN1 | 8876 | vanin 1 | O95497 |
C1306459 | Primary malignant neoplasm | VNN1 | 8876 | vanin 1 | O95497 |
C0009402 | Colorectal Carcinoma | VNN1 | 8876 | vanin 1 | O95497 |
C0178664 | Glomerulosclerosis (disorder) | VNN1 | 8876 | vanin 1 | O95497 |
C0149939 | Obstructive nephropathy | VNN1 | 8876 | vanin 1 | O95497 |
C0004153 | Atherosclerosis | VNN1 | 8876 | vanin 1 | O95497 |
C0699790 | Colon Carcinoma | VNN1 | 8876 | vanin 1 | O95497 |
C0020538 | Hypertensive disease | VNN1 | 8876 | vanin 1 | O95497 |
C0041956 | Ureteral obstruction | VNN1 | 8876 | vanin 1 | O95497 |
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Last updated: August 19, 2024