pigmentation disease

Summary
Definition
A skin disease that is characterized by discoloration of the skin.
Super Class
skin disease
Disease Ontology
DOID:10123
UMLS
Related Genes
Displaying entries 1 - 10 of 13 in total
Gene ID Gene Symbol Description Source
434 ASIP agouti signaling protein
2006 ELN elastin
3662 IRF4 interferon regulatory factor 4
4157 MC1R melanocortin 1 receptor
4254 KITLG KIT ligand
4318 MMP9 matrix metallopeptidase 9
4948 OCA2 OCA2 melanosomal transmembrane protein
7299 TYR tyrosinase
7306 TYRP1 tyrosinase related protein 1
8924 HERC2 HECT and RLD domain containing E3 ubiquitin protein ligase 2
Displaying entry 11 - 11 of 11 in total
Gene ID Gene Symbol Description Source
238384 Slc24a4 solute carrier family 24 (sodium/potassium/calcium exchanger), member 4
Displaying all 3 entries
Gene ID Gene Symbol Description Source
24152 Asip agouti signaling protein
60427 Kitlg KIT ligand
81687 Mmp9 matrix metallopeptidase 9
Displaying 1 entry
Gene ID Gene Symbol Description Source
777614 tpcn2 two pore segment channel 2
Displaying all 3 entries
Gene ID Gene Symbol Description Source
176105 tyr-1 Putative tyrosinase-like protein tyr-1
179991 zmp-4 Hemopexin;Peptidase metallopeptidase domain-containing protein
180351 W01F3.2 Uncharacterized protein

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 v4.1.0

Last updated: December 9, 2024