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 ▼ |
---|---|---|---|---|---|
C0346647 | Malignant neoplasm of pancreas | SEMA7A | 8482 | semaphorin 7A (John Milton Hagen blood group) | O75326 |
C0033999 | Pterygium | SEMA7A | 8482 | semaphorin 7A (John Milton Hagen blood group) | O75326 |
C0085413 | Polycystic Kidney, Autosomal Dominant | SEMA7A | 8482 | semaphorin 7A (John Milton Hagen blood group) | O75326 |
C0038454 | Cerebrovascular accident | SEMA7A | 8482 | semaphorin 7A (John Milton Hagen blood group) | O75326 |
C0235974 | Pancreatic carcinoma | SEMA7A | 8482 | semaphorin 7A (John Milton Hagen blood group) | O75326 |
C0027765 | nervous system disorder | SEMA7A | 8482 | semaphorin 7A (John Milton Hagen blood group) | O75326 |
C0678222 | Breast Carcinoma | SEMA7A | 8482 | semaphorin 7A (John Milton Hagen blood group) | O75326 |
C0014070 | Encephalomyelitis | SEMA7A | 8482 | semaphorin 7A (John Milton Hagen blood group) | O75326 |
C0036220 | Kaposi Sarcoma | SEMA7A | 8482 | semaphorin 7A (John Milton Hagen blood group) | O75326 |
C0025202 | melanoma | SEMA7A | 8482 | semaphorin 7A (John Milton Hagen blood group) | O75326 |
C0017638 | Glioma | SEMA7A | 8482 | semaphorin 7A (John Milton Hagen blood group) | O75326 |
C1527336 | Sjogren's Syndrome | SEMA7A | 8482 | semaphorin 7A (John Milton Hagen blood group) | O75326 |
C0206062 | Lung Diseases, Interstitial | SEMA7A | 8482 | semaphorin 7A (John Milton Hagen blood group) | O75326 |
C1800706 | Idiopathic Pulmonary Fibrosis | SEMA7A | 8482 | semaphorin 7A (John Milton Hagen blood group) | O75326 |
C0014556 | Epilepsy, Temporal Lobe | SEMA7A | 8482 | semaphorin 7A (John Milton Hagen blood group) | O75326 |
C0007124 | Noninfiltrating Intraductal Carcinoma | SEMA7A | 8482 | semaphorin 7A (John Milton Hagen blood group) | O75326 |
C0376358 | Malignant neoplasm of prostate | UGT2B11 | 10720 | UDP glucuronosyltransferase family 2 member B11 | O75310 |
C0345905 | Intrahepatic Cholangiocarcinoma | UGT2B11 | 10720 | UDP glucuronosyltransferase family 2 member B11 | O75310 |
C0948008 | Ischemic stroke | XYLB | 9942 | xylulokinase | O75191 |
C0410174 | Fukuyama Type Congenital Muscular Dystrophy | FKTN | 2218 | fukutin | O75072 |
C0003466 | Anus, Imperforate | FKTN | 2218 | fukutin | O75072 |
C0521694 | Atrophic retina | FKTN | 2218 | fukutin | O75072 |
C0265221 | Walker-Warburg congenital muscular dystrophy | FKTN | 2218 | fukutin | O75072 |
C0006826 | Malignant Neoplasms | FKTN | 2218 | fukutin | O75072 |
C0025362 | Mental Retardation | FKTN | 2218 | fukutin | O75072 |
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