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 45301 - 45325 of 62743 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Gene Name UniProt ID
C3714756 Intellectual Disability CYP2U1 113612 cytochrome P450 family 2 subfamily U member 1 Q7Z449
C4721453 Peripheral Nervous System Diseases CYP2U1 113612 cytochrome P450 family 2 subfamily U member 1 Q7Z449
C0520947 Clumsiness - motor delay CYP2U1 113612 cytochrome P450 family 2 subfamily U member 1 Q7Z449
C0013421 Dystonia CYP2U1 113612 cytochrome P450 family 2 subfamily U member 1 Q7Z449
C0006142 Malignant neoplasm of breast CYP2U1 113612 cytochrome P450 family 2 subfamily U member 1 Q7Z449
C0152444 Hydrorhachis CYP2U1 113612 cytochrome P450 family 2 subfamily U member 1 Q7Z449
C0006826 Malignant Neoplasms CYP2U1 113612 cytochrome P450 family 2 subfamily U member 1 Q7Z449
C0042798 Low Vision CYP2U1 113612 cytochrome P450 family 2 subfamily U member 1 Q7Z449
C0393593 Dystonia Disorders CYP2U1 113612 cytochrome P450 family 2 subfamily U member 1 Q7Z449
C0678222 Breast Carcinoma CYP2U1 113612 cytochrome P450 family 2 subfamily U member 1 Q7Z449
C0699790 Colon Carcinoma CYP2R1 120227 cytochrome P450 family 2 subfamily R member 1 Q6VVX0
C0004096 Asthma CYP2R1 120227 cytochrome P450 family 2 subfamily R member 1 Q6VVX0
C0042870 Vitamin D Deficiency CYP2R1 120227 cytochrome P450 family 2 subfamily R member 1 Q6VVX0
C0239946 Fibrosis, Liver CYP2R1 120227 cytochrome P450 family 2 subfamily R member 1 Q6VVX0
C0238463 Papillary thyroid carcinoma CYP2R1 120227 cytochrome P450 family 2 subfamily R member 1 Q6VVX0
C0001418 Adenocarcinoma CYP2R1 120227 cytochrome P450 family 2 subfamily R member 1 Q6VVX0
C0024894 Mastitis CYP2R1 120227 cytochrome P450 family 2 subfamily R member 1 Q6VVX0
C0026269 Mitral Valve Stenosis CYP2R1 120227 cytochrome P450 family 2 subfamily R member 1 Q6VVX0
C0085584 Encephalopathies CYP2R1 120227 cytochrome P450 family 2 subfamily R member 1 Q6VVX0
C0242383 Age related macular degeneration CYP2R1 120227 cytochrome P450 family 2 subfamily R member 1 Q6VVX0
C0007137 Squamous cell carcinoma CYP2R1 120227 cytochrome P450 family 2 subfamily R member 1 Q6VVX0
C0600139 Prostate carcinoma CYP2R1 120227 cytochrome P450 family 2 subfamily R member 1 Q6VVX0
C0035579 Rickets CYP2R1 120227 cytochrome P450 family 2 subfamily R member 1 Q6VVX0
C1337013 Differentiated Thyroid Gland Carcinoma CYP2R1 120227 cytochrome P450 family 2 subfamily R member 1 Q6VVX0
C0346647 Malignant neoplasm of pancreas CYP2R1 120227 cytochrome P450 family 2 subfamily R member 1 Q6VVX0

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