DisGeNET

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
Displaying entries 39726 - 39750 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C1458155 Mammary Neoplasms AKR1C2 1646 aldo-keto reductase family 1 member C2 P52895
C0006142 Malignant neoplasm of breast AKR1C2 1646 aldo-keto reductase family 1 member C2 P52895
C0345904 Malignant neoplasm of liver AKR1C2 1646 aldo-keto reductase family 1 member C2 P52895
C0032460 Polycystic Ovary Syndrome AKR1C2 1646 aldo-keto reductase family 1 member C2 P52895
C0238395 Male Pseudohermaphroditism AKR1C2 1646 aldo-keto reductase family 1 member C2 P52895
C0279626 Squamous cell carcinoma of esophagus AKR1C2 1646 aldo-keto reductase family 1 member C2 P52895
C1306459 Primary malignant neoplasm AKR1C2 1646 aldo-keto reductase family 1 member C2 P52895
C0268398 Familial lichen amyloidosis AKR1C2 1646 aldo-keto reductase family 1 member C2 P52895
C0006826 Malignant Neoplasms AKR1C2 1646 aldo-keto reductase family 1 member C2 P52895
C0678222 Breast Carcinoma AKR1C2 1646 aldo-keto reductase family 1 member C2 P52895
C0011430 Dentin Dysplasia AKR1C2 1646 aldo-keto reductase family 1 member C2 P52895
C0600139 Prostate carcinoma AKR1C2 1646 aldo-keto reductase family 1 member C2 P52895
C0005695 Bladder Neoplasm AKR1C2 1646 aldo-keto reductase family 1 member C2 P52895
C0042131 Uterine Diseases AKR1C2 1646 aldo-keto reductase family 1 member C2 P52895
C0399378 Dentinogenesis imperfecta - Shield's type III (disorder) AKR1C2 1646 aldo-keto reductase family 1 member C2 P52895
C0007137 Squamous cell carcinoma AKR1C2 1646 aldo-keto reductase family 1 member C2 P52895
C2930618 Intersex Conditions AKR1C2 1646 aldo-keto reductase family 1 member C2 P52895
C0269102 Endometrioma AKR1C2 1646 aldo-keto reductase family 1 member C2 P52895
C2973527 Dentinogenesis imperfecta without osteogenesis imperfecta AKR1C2 1646 aldo-keto reductase family 1 member C2 P52895
C0033804 Pseudohermaphroditism AKR1C2 1646 aldo-keto reductase family 1 member C2 P52895
C0036875 Disorders of Sex Development AKR1C2 1646 aldo-keto reductase family 1 member C2 P52895
C0376358 Malignant neoplasm of prostate AKR1C2 1646 aldo-keto reductase family 1 member C2 P52895
C0007131 Non-Small Cell Lung Carcinoma AKR1C2 1646 aldo-keto reductase family 1 member C2 P52895
C0004763 Barrett Esophagus AKR1C2 1646 aldo-keto reductase family 1 member C2 P52895
C0011581 Depressive disorder AKR1C2 1646 aldo-keto reductase family 1 member C2 P52895

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024