abnormal hair laboratory examination Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003328
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Genes

15 genes associated with the abnormal hair laboratory examination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ASL argininosuccinate lyase
BCS1L BC1 (ubiquinol-cytochrome c reductase) synthesis-like
CDH3 cadherin 3, type 1, P-cadherin (placental)
DSG4 desmoglein 4
FOXE1 forkhead box E1
HR hair growth associated
KRT85 keratin 85, type II
MPLKIP M-phase specific PLK1 interacting protein
PVRL1 poliovirus receptor-related 1 (herpesvirus entry mediator C)
PVRL4 poliovirus receptor-related 4
SKIV2L superkiller viralicidic activity 2-like (S. cerevisiae)
ST14 suppression of tumorigenicity 14 (colon carcinoma)
TP63 tumor protein p63
TTC37 tetratricopeptide repeat domain 37
WRN Werner syndrome, RecQ helicase-like