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 46751 - 46775 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0678222 Breast Carcinoma SQLE 6713 squalene epoxidase Q14534
C0027651 Neoplasms SQLE 6713 squalene epoxidase Q14534
C0149782 Squamous cell carcinoma of lung SQLE 6713 squalene epoxidase Q14534
C1458155 Mammary Neoplasms SQLE 6713 squalene epoxidase Q14534
C0376358 Malignant neoplasm of prostate SQLE 6713 squalene epoxidase Q14534
C0006826 Malignant Neoplasms SQLE 6713 squalene epoxidase Q14534
C1306459 Primary malignant neoplasm SQLE 6713 squalene epoxidase Q14534
C0003811 Cardiac Arrhythmia SQLE 6713 squalene epoxidase Q14534
C0023976 Long QT Syndrome SQLE 6713 squalene epoxidase Q14534
C0022602 Actinic keratosis INPP5A 3632 inositol polyphosphate-5-phosphatase A Q14642
C0008313 Cholangitis, Sclerosing INPP5A 3632 inositol polyphosphate-5-phosphatase A Q14642
C0553723 Squamous cell carcinoma of skin INPP5A 3632 inositol polyphosphate-5-phosphatase A Q14642
C0028860 Oculocerebrorenal Syndrome INPP5A 3632 inositol polyphosphate-5-phosphatase A Q14642
C0007137 Squamous cell carcinoma INPP5A 3632 inositol polyphosphate-5-phosphatase A Q14642
C0036341 Schizophrenia INPP5A 3632 inositol polyphosphate-5-phosphatase A Q14642
C0007114 Malignant neoplasm of skin INPP5A 3632 inositol polyphosphate-5-phosphatase A Q14642
C0027651 Neoplasms INPP5A 3632 inositol polyphosphate-5-phosphatase A Q14642
C0011847 Diabetes LPIN1 23175 lipin 1 Q14693
C0023787 Lipodystrophy LPIN1 23175 lipin 1 Q14693
C2711227 Steatohepatitis LPIN1 23175 lipin 1 Q14693
C1306459 Primary malignant neoplasm LPIN1 23175 lipin 1 Q14693
C0015696 Fatty Liver, Alcoholic LPIN1 23175 lipin 1 Q14693
C0032460 Polycystic Ovary Syndrome LPIN1 23175 lipin 1 Q14693
C0007102 Malignant tumor of colon LPIN1 23175 lipin 1 Q14693
C1849386 Myoglobinuria, Acute Recurrent, Autosomal Recessive LPIN1 23175 lipin 1 Q14693

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