hypotrichosis Gene Set

Dataset DISEASES Curated Gene-Disease Assocation 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