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
Similar Terms
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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
