abnormal hair follicle inner root sheath morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the multilayered tube composed of terminally differentiated hair follicle keratinocytes that is surrounded by the outer root sheath; the layers of the inner root sheath include the companion layer, Henle's layer, Huxley's layer and the inner root sheath cuticle (Mammalian Phenotype Ontology, MP_0010685)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010685
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Genes

15 gene mutations causing the abnormal hair follicle inner root sheath morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
C8ORF44-SGK3 C8orf44-SGK3 readthrough
CDC42 cell division cycle 42
CUX1 cut-like homeobox 1
DSG4 desmoglein 4
EGFR epidermal growth factor receptor
FOXN1 forkhead box N1
HR hair growth associated
KRT25 keratin 25, type I
KRT71 keratin 71, type II
KSR1 kinase suppressor of ras 1
LIPH lipase, member H
PKP3 plakophilin 3
SCD stearoyl-CoA desaturase (delta-9-desaturase)
SHH sonic hedgehog
SP6 Sp6 transcription factor