dysphonia Gene Set
Genes
16 genes associated with the dysphonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
BIN1
|
bridging integrator 1
|
|
C10ORF2
|
chromosome 10 open reading frame 2
|
|
CYP27A1
|
cytochrome P450, family 27, subfamily A, polypeptide 1
|
|
EDA
|
ectodysplasin A
|
|
FTL
|
ferritin, light polypeptide
|
|
GNAL
|
guanine nucleotide binding protein (G protein), alpha activating activity polypeptide, olfactory type
|
|
LMNB1
|
lamin B1
|
|
MGME1
|
mitochondrial genome maintenance exonuclease 1
|
|
NOTCH3
|
notch 3
|
|
PANK2
|
pantothenate kinase 2
|
|
POLG
|
polymerase (DNA directed), gamma
|
|
PRKRA
|
protein kinase, interferon-inducible double stranded RNA dependent activator
|
|
SOD1
|
superoxide dismutase 1, soluble
|
|
THAP1
|
THAP domain containing, apoptosis associated protein 1
|
|
TTC19
|
tetratricopeptide repeat domain 19
|
|
TUBB4A
|
tubulin, beta 4A class IVa
|
