rhinitis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A upper respiratory infectious disease which involves irritation and inflammation of the mucous membrane of the nose due to viruses, bacteria or irritants. The inflammation results in generation of excessive amounts of mucus leading to runny nose, as well as nasal congestion and post-nasal drip. (Human Disease Ontology, DOID_4483)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012384
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Genes

19 genes associated with the rhinitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ARMC4 armadillo repeat containing 4
C21ORF59 chromosome 21 open reading frame 59
CCDC103 coiled-coil domain containing 103
CCDC65 coiled-coil domain containing 65
COX4I2 cytochrome c oxidase subunit IV isoform 2 (lung)
DNAAF5 dynein, axonemal, assembly factor 5
DNAI1 dynein, axonemal, intermediate chain 1
DNAI2 dynein, axonemal, intermediate chain 2
DNAL1 dynein, axonemal, light chain 1
HYDIN HYDIN, axonemal central pair apparatus protein
LRRC6 leucine rich repeat containing 6
PGM3 phosphoglucomutase 3
PLCG2 phospholipase C, gamma 2 (phosphatidylinositol-specific)
RSPH1 radial spoke head 1 homolog (Chlamydomonas)
RSPH4A radial spoke head 4 homolog A (Chlamydomonas)
RSPH9 radial spoke head 9 homolog (Chlamydomonas)
SPAG1 sperm associated antigen 1
TNFSF11 tumor necrosis factor (ligand) superfamily, member 11
ZMYND10 zinc finger, MYND-type containing 10