hypotrichosis Gene Set

Dataset	DISEASES Curated Gene-Disease Association Evidence Scores
Category	disease or phenotype associations
Type	disease
Description	A hair disease that is characterized by sparse hair on the scalp resulting from abnormal hair follicle development and has_material_basis in mutations in proteins involved in hair growth, division or proliferation of cells within hair follicles. (Human Disease Ontology, DOID_4535)
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Genes

21 genes involed in the disease hypotrichosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol	Name
ANTXR1	anthrax toxin receptor 1
APCDD1	adenomatosis polyposis coli down-regulated 1
CDH3	cadherin 3, type 1, P-cadherin (placental)
CDSN	corneodesmosin
DSC3	desmocollin 3
DSG1	desmoglein 1
DSG4	desmoglein 4
HR	hair growth associated
KRT71	keratin 71, type II
KRT74	keratin 74, type II
KRT85	keratin 85, type II
LIPH	lipase, member H
LPAR6	lysophosphatidic acid receptor 6
POC1A	POC1 centriolar protein A
RPL21	ribosomal protein L21
SMARCA2	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2
SNRPE	small nuclear ribonucleoprotein polypeptide E
SOX18	SRY (sex determining region Y)-box 18
SPINK5	serine peptidase inhibitor, Kazal type 5
ST14	suppression of tumorigenicity 14 (colon carcinoma)
WNT10A	wingless-type MMTV integration site family, member 10A