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 |
---|---|---|---|---|---|
C0017601 | Glaucoma | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
C0008055 | Chikungunya Fever | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
C0242006 | Myelofibrosis due to another disorder | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
C0020538 | Hypertensive disease | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
C1839840 | MALE PSEUDOHERMAPHRODITISM: DEFICIENCY OF TESTICULAR 17,20-DESMOLASE | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
C0021400 | Influenza | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
C0409974 | Lupus Erythematosus | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
C0279000 | Liver and Intrahepatic Biliary Tract Carcinoma | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
C0032463 | Polycythemia Vera | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
C0024301 | Lymphoma, Follicular | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
C4551720 | Primary Ciliary Dyskinesia | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
C1843013 | Alzheimer disease, familial, type 3 | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
C0024141 | Lupus Erythematosus, Systemic | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
C0010417 | Cryptorchidism | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
C0023467 | Leukemia, Myelocytic, Acute | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
C0002871 | Anemia | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
C0024138 | Lupus Erythematosus, Discoid | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
C0338831 | Manic | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
C1332977 | Childhood Leukemia | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
C0005695 | Bladder Neoplasm | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
C0006826 | Malignant Neoplasms | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
C0162311 | Androgenetic Alopecia | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
C0000768 | Congenital Abnormality | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
C0029456 | Osteoporosis | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
C1456784 | Paranoia | AKR1C4 | 1109 | aldo-keto reductase family 1 member C4 | P17516 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024