Alopecia Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A hypotrichosis that is characterized by a loss of hair from the head or body. (Human Disease Ontology, DOID_987)
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Genes

31 genes associated with the Alopecia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1
AGA aspartylglucosaminidase
AR androgen receptor
BTNL2 butyrophilin-like 2
CACNB4 calcium channel, voltage-dependent, beta 4 subunit
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
CYP3A4 cytochrome P450, family 3, subfamily A, polypeptide 4
CYP3A43 cytochrome P450, family 3, subfamily A, polypeptide 43
CYP3A5 cytochrome P450, family 3, subfamily A, polypeptide 5
EDA2R ectodysplasin A2 receptor
ERCC1 excision repair cross-complementation group 1
ERCC2 excision repair cross-complementation group 2
ESR1 estrogen receptor 1
ESR2 estrogen receptor 2 (ER beta)
GSTM1 glutathione S-transferase mu 1
GSTP1 glutathione S-transferase pi 1
GSTT1 glutathione S-transferase theta 1
HDAC9 histone deacetylase 9
HLA-DQA1 major histocompatibility complex, class II, DQ alpha 1
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
HLA-DRB5 major histocompatibility complex, class II, DR beta 5
HR hair growth associated
LINC01432 long intergenic non-protein coding RNA 1432
PGR progesterone receptor
PMS2 PMS2 postmeiotic segregation increased 2 (S. cerevisiae)
SRD5A1 steroid-5-alpha-reductase, alpha polypeptide 1 (3-oxo-5 alpha-steroid delta 4-dehydrogenase alpha 1)
SRD5A2 steroid-5-alpha-reductase, alpha polypeptide 2 (3-oxo-5 alpha-steroid delta 4-dehydrogenase alpha 2)
TLR1 toll-like receptor 1
TPMT thiopurine S-methyltransferase
WNT10A wingless-type MMTV integration site family, member 10A