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 |
---|---|---|---|---|---|
C0153633 | Malignant neoplasm of brain | ALDH1A3 | 220 | aldehyde dehydrogenase 1 family member A3 | P47895 |
C0006118 | Brain Neoplasms | ALDH1A3 | 220 | aldehyde dehydrogenase 1 family member A3 | P47895 |
C0038356 | Stomach Neoplasms | ALDH1A3 | 220 | aldehyde dehydrogenase 1 family member A3 | P47895 |
C0007131 | Non-Small Cell Lung Carcinoma | ALDH1A3 | 220 | aldehyde dehydrogenase 1 family member A3 | P47895 |
C0017636 | Glioblastoma | ALDH1A3 | 220 | aldehyde dehydrogenase 1 family member A3 | P47895 |
C0009363 | Congenital ocular coloboma (disorder) | ALDH1A3 | 220 | aldehyde dehydrogenase 1 family member A3 | P47895 |
C0009375 | Colonic Neoplasms | ALDH1A3 | 220 | aldehyde dehydrogenase 1 family member A3 | P47895 |
C3714506 | Meckel syndrome type 1 | ALDH1A3 | 220 | aldehyde dehydrogenase 1 family member A3 | P47895 |
C0009402 | Colorectal Carcinoma | ALDH1A3 | 220 | aldehyde dehydrogenase 1 family member A3 | P47895 |
C0684249 | Carcinoma of lung | ALDH1A3 | 220 | aldehyde dehydrogenase 1 family member A3 | P47895 |
C0235974 | Pancreatic carcinoma | ALDH1A3 | 220 | aldehyde dehydrogenase 1 family member A3 | P47895 |
C0032580 | Adenomatous Polyposis Coli | ALDH1A3 | 220 | aldehyde dehydrogenase 1 family member A3 | P47895 |
C0238463 | Papillary thyroid carcinoma | ALDH1A3 | 220 | aldehyde dehydrogenase 1 family member A3 | P47895 |
C2711227 | Steatohepatitis | ALDH1A3 | 220 | aldehyde dehydrogenase 1 family member A3 | P47895 |
C1458155 | Mammary Neoplasms | ALDH1A3 | 220 | aldehyde dehydrogenase 1 family member A3 | P47895 |
C4551977 | Microphthalmos, Autosomal Recessive | ALDH1A3 | 220 | aldehyde dehydrogenase 1 family member A3 | P47895 |
C1514422 | Glioblastoma, IDH-Wildtype | ALDH1A3 | 220 | aldehyde dehydrogenase 1 family member A3 | P47895 |
C1856127 | Bile acid synthesis defect, congenital, 2 | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
C0019158 | Hepatitis | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
C0011849 | Diabetes Mellitus | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
C0000768 | Congenital Abnormality | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
C0019159 | Hepatitis A | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
C0392514 | Hereditary hemochromatosis | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
C0029456 | Osteoporosis | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
C0023895 | Liver diseases | AKR1D1 | 6718 | aldo-keto reductase family 1 member D1 | P51857 |
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