abnormal dermal pigmentation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the coloration of the dermal layer of the skin due to changes in the amount, shape, or distribution of cells producing pigment (Mammalian Phenotype Ontology, MP_0009385)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009385
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Genes

3 gene mutations causing the abnormal dermal pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BRAF B-Raf proto-oncogene, serine/threonine kinase
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
SLC24A5 solute carrier family 24 (sodium/potassium/calcium exchanger), member 5