abnormal hair follicle melanin granule morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the pigment particles in the hair follicles (Mammalian Phenotype Ontology, MP_0005072)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005072
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Genes

9 gene mutations causing the abnormal hair follicle melanin granule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADAMTS20 ADAM metallopeptidase with thrombospondin type 1 motif, 20
BCL2 B-cell CLL/lymphoma 2
BLOC1S3 biogenesis of lysosomal organelles complex-1, subunit 3
ELOVL3 ELOVL fatty acid elongase 3
KRT17 keratin 17, type I
LEF1 lymphoid enhancer-binding factor 1
LYST lysosomal trafficking regulator
SOX10 SRY (sex determining region Y)-box 10
TYR tyrosinase