follicular hyperkeratosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A skin condition characterized by excessive development of keratin in hair follicles, resulting in rough, cone-shaped, elevated papules resulting from closure of hair follicles with a white plug of sebum. (Human Phenotype Ontology, HP_0007502)
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8 genes associated with the follicular hyperkeratosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
COL6A1 collagen, type VI, alpha 1
COL6A2 collagen, type VI, alpha 2
COL6A3 collagen, type VI, alpha 3
DSG4 desmoglein 4
FKBP14 FK506 binding protein 14, 22 kDa
KRT16 keratin 16, type I
MBTPS2 membrane-bound transcription factor peptidase, site 2
SAT1 spermidine/spermine N1-acetyltransferase 1