absent hair follicle melanin granules Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the pigment polymers located in the hair follicles (Mammalian Phenotype Ontology, MP_0000394)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000394
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Genes

5 gene mutations causing the absent hair follicle melanin granules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BCL2 B-cell CLL/lymphoma 2
LEF1 lymphoid enhancer-binding factor 1
LYST lysosomal trafficking regulator
SOX10 SRY (sex determining region Y)-box 10
TYR tyrosinase