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 60401 - 60425 of 62743 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Gene Name UniProt ID
C0033578 Prostatic Neoplasms ACSM3 6296 acyl-CoA synthetase medium chain family member 3 Q53FZ2
C0007766 Intracranial Aneurysm ACSM3 6296 acyl-CoA synthetase medium chain family member 3 Q53FZ2
C0040028 Thrombocythemia, Essential ACSM3 6296 acyl-CoA synthetase medium chain family member 3 Q53FZ2
C1561643 Chronic Kidney Diseases ACSM3 6296 acyl-CoA synthetase medium chain family member 3 Q53FZ2
C0039685 Tetralogy of Fallot ACSM3 6296 acyl-CoA synthetase medium chain family member 3 Q53FZ2
C0376358 Malignant neoplasm of prostate ACSM3 6296 acyl-CoA synthetase medium chain family member 3 Q53FZ2
C0019114 Hemosiderosis ACSM3 6296 acyl-CoA synthetase medium chain family member 3 Q53FZ2
C0020255 Hydrocephalus ACSM3 6296 acyl-CoA synthetase medium chain family member 3 Q53FZ2
C0006826 Malignant Neoplasms ACSM3 6296 acyl-CoA synthetase medium chain family member 3 Q53FZ2
C0020456 Hyperglycemia ACSM3 6296 acyl-CoA synthetase medium chain family member 3 Q53FZ2
C1510586 Autism Spectrum Disorders ACSM3 6296 acyl-CoA synthetase medium chain family member 3 Q53FZ2
C0038436 Post-Traumatic Stress Disorder ACSM3 6296 acyl-CoA synthetase medium chain family member 3 Q53FZ2
C0024796 Marfan Syndrome ACSM3 6296 acyl-CoA synthetase medium chain family member 3 Q53FZ2
C0751003 Brain Aneurysm ACSM3 6296 acyl-CoA synthetase medium chain family member 3 Q53FZ2
C0265110 Cerebral Vasospasm ACSM3 6296 acyl-CoA synthetase medium chain family member 3 Q53FZ2
C0006142 Malignant neoplasm of breast ACSM3 6296 acyl-CoA synthetase medium chain family member 3 Q53FZ2
C0345904 Malignant neoplasm of liver ACSM3 6296 acyl-CoA synthetase medium chain family member 3 Q53FZ2
C0006118 Brain Neoplasms ACSM3 6296 acyl-CoA synthetase medium chain family member 3 Q53FZ2
C0751494 Convulsive Seizures ACSM3 6296 acyl-CoA synthetase medium chain family member 3 Q53FZ2
C0162531 Hereditary Coproporphyria ACSM3 6296 acyl-CoA synthetase medium chain family member 3 Q53FZ2
C0007789 Cerebral Palsy ACSM2A 123876 acyl-CoA synthetase medium chain family member 2A Q08AH3
C0524620 Metabolic Syndrome X ACSM1 116285 acyl-CoA synthetase medium chain family member 1 Q08AH1
C0007789 Cerebral Palsy ACSM1 116285 acyl-CoA synthetase medium chain family member 1 Q08AH1
C0041696 Unipolar Depression ACSM1 116285 acyl-CoA synthetase medium chain family member 1 Q08AH1
C0036341 Schizophrenia ACSM1 116285 acyl-CoA synthetase medium chain family member 1 Q08AH1

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