abnormal epidermal pigmentation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the coloration of the epidermal layer of the skin due to changes in the amount, shape, or distribution of cells producing pigment (Mammalian Phenotype Ontology, MP_0009387)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009387
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9 gene mutations causing the abnormal epidermal pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCA4 ATP-binding cassette, sub-family A (ABC1), member 4
CBX6 chromobox homolog 6
DUSP1 dual specificity phosphatase 1
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
IL22RA1 interleukin 22 receptor, alpha 1
LMNA lamin A/C
MYO7A myosin VIIA
SLC24A5 solute carrier family 24 (sodium/potassium/calcium exchanger), member 5
USP4 ubiquitin specific peptidase 4 (proto-oncogene)