mixed hearing impairment Gene Set
Genes
16 genes associated with the mixed hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
ANKH
|
ANKH inorganic pyrophosphate transport regulator
|
|
CHD7
|
chromodomain helicase DNA binding protein 7
|
|
COL11A2
|
collagen, type XI, alpha 2
|
|
COL2A1
|
collagen, type II, alpha 1
|
|
EYA1
|
EYA transcriptional coactivator and phosphatase 1
|
|
FAM20C
|
family with sequence similarity 20, member C
|
|
FGF10
|
fibroblast growth factor 10
|
|
FGFR2
|
fibroblast growth factor receptor 2
|
|
FGFR3
|
fibroblast growth factor receptor 3
|
|
FLNB
|
filamin B, beta
|
|
GDF6
|
growth differentiation factor 6
|
|
GJA1
|
gap junction protein, alpha 1, 43kDa
|
|
HOXA2
|
homeobox A2
|
|
PAX1
|
paired box 1
|
|
PORCN
|
porcupine homolog (Drosophila)
|
|
SEMA3E
|
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
|
