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Standards Ontologies Notations
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 11 - 13 of 13 in total
Gene ID Gene Symbol Description Source
51151 SLC45A2 solute carrier family 45 member 2
123041 SLC24A4 solute carrier family 24 member 4
219931 TPCN2 two pore segment channel 2
Displaying entries 1 - 10 of 11 in total
Gene ID Gene Symbol Description Source
15204 Herc2 HECT and RLD domain containing E3 ubiquitin protein ligase 2
17199 Mc1r melanocortin 1 receptor
17311 Kitl kit ligand
17395 Mmp9 matrix metallopeptidase 9
18431 Oca2 oculocutaneous albinism II
22173 Tyr tyrosinase
22178 Tyrp1 tyrosinase-related protein 1
22293 Slc45a2 solute carrier family 45, member 2
50518 a nonagouti
233979 Tpcn2 two pore segment channel 2
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
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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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

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Last updated: December 9, 2024