abnormal hair follicle bulb morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the thickened portion of the proximal portion of the hair follicle that contains rapidly proliferating matrix cells, melanocytes and outer root sheath cells (Mammalian Phenotype Ontology, MP_0010681)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010681
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Genes

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

Symbol Name
ARNTL aryl hydrocarbon receptor nuclear translocator-like
C8ORF44-SGK3 C8orf44-SGK3 readthrough
CDC42 cell division cycle 42
EN1 engrailed homeobox 1
FGF10 fibroblast growth factor 10
FOXN1 forkhead box N1
HR hair growth associated
ITGB2 integrin, beta 2 (complement component 3 receptor 3 and 4 subunit)
KRT17 keratin 17, type I
SCD stearoyl-CoA desaturase (delta-9-desaturase)