sparse scalp hair Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Decreased number of head hairs per unit area. (Human Phenotype Ontology, HP_0002209)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002209
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Genes

22 genes associated with the sparse scalp hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ARID1A AT rich interactive domain 1A (SWI-like)
AXIN2 axin 2
B3GALT6 UDP-Gal:betaGal beta 1,3-galactosyltransferase polypeptide 6
B4GALT7 xylosylprotein beta 1,4-galactosyltransferase, polypeptide 7
CDH3 cadherin 3, type 1, P-cadherin (placental)
DSC3 desmocollin 3
FIG4 FIG4 phosphoinositide 5-phosphatase
KAT6B K(lysine) acetyltransferase 6B
KRT17 keratin 17, type I
LMNA lamin A/C
LPAR6 lysophosphatidic acid receptor 6
NOP10 NOP10 ribonucleoprotein
PCNT pericentrin
PVRL4 poliovirus receptor-related 4
RNU4ATAC RNA, U4atac small nuclear (U12-dependent splicing)
SHOC2 soc-2 suppressor of clear homolog (C. elegans)
SMARCA2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2
SMARCA4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4
SPINK5 serine peptidase inhibitor, Kazal type 5
TP63 tumor protein p63
UBR1 ubiquitin protein ligase E3 component n-recognin 1
WNT10A wingless-type MMTV integration site family, member 10A