abnormal hair follicle melanocyte morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the cells that produce pigment in the hair follicles (Mammalian Phenotype Ontology, MP_0004381)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004381
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Genes

15 gene mutations causing the abnormal hair follicle melanocyte 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
EDA ectodysplasin A
EDNRB endothelin receptor type B
ELOVL3 ELOVL fatty acid elongase 3
KRT17 keratin 17, type I
LEF1 lymphoid enhancer-binding factor 1
LYST lysosomal trafficking regulator
MC1R melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor)
MITF microphthalmia-associated transcription factor
MLANA melan-A
MPZL3 myelin protein zero-like 3
SOX10 SRY (sex determining region Y)-box 10
TYR tyrosinase