abnormality of the nasal mucosa Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000433
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13 genes associated with the abnormality of the nasal mucosa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACVRL1 activin A receptor type II-like 1
DNAAF3 dynein, axonemal, assembly factor 3
DNAI1 dynein, axonemal, intermediate chain 1
ECM1 extracellular matrix protein 1
ENG endoglin
HYDIN HYDIN, axonemal central pair apparatus protein
LRRC6 leucine rich repeat containing 6
STK11 serine/threonine kinase 11
TAP1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)
TAP2 transporter 2, ATP-binding cassette, sub-family B (MDR/TAP)
TAPBP TAP binding protein (tapasin)
TBX21 T-box 21
ZMYND10 zinc finger, MYND-type containing 10