Abnormality Of The Voice Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Any abnormality of the voice. (Human Phenotype Ontology, HP_0001608)
External Link https://www.disgenet.org/browser/0/1/0/C4021776
Similar Terms
Downloads & Tools

Genes

64 genes associated with the disease Abnormality Of The Voice in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ALPL alkaline phosphatase, liver/bone/kidney
ANOS1 anosmin 1
AP4E1 adaptor-related protein complex 4, epsilon 1 subunit
B3GALNT2 beta-1,3-N-acetylgalactosaminyltransferase 2
BRAF B-Raf proto-oncogene, serine/threonine kinase
CCDC141 coiled-coil domain containing 141
CHD7 chromodomain helicase DNA binding protein 7
DCC DCC netrin 1 receptor
DLEC1 deleted in lung and esophageal cancer 1
DUSP6 dual specificity phosphatase 6
EIF4A3 eukaryotic translation initiation factor 4A3
FEZF1 FEZ family zinc finger 1
FGF17 fibroblast growth factor 17
FGF8 fibroblast growth factor 8 (androgen-induced)
FGFR1 fibroblast growth factor receptor 1
FHL1 four and a half LIM domains 1
FKRP fukutin related protein
FKTN fukutin
FLRT3 fibronectin leucine rich transmembrane protein 3
GMPPB GDP-mannose pyrophosphorylase B
GNRH1 gonadotropin-releasing hormone 1 (luteinizing-releasing hormone)
GNRHR gonadotropin-releasing hormone receptor
HESX1 HESX homeobox 1
HS6ST1 heparan sulfate 6-O-sulfotransferase 1
HTT huntingtin
IL17RD interleukin 17 receptor D
KISS1 KiSS-1 metastasis-suppressor
KISS1R KISS1 receptor
LARGE like-glycosyltransferase
LMNA lamin A/C
NLRP3 NLR family, pyrin domain containing 3
NOTCH2 notch 2
NSMF NMDA receptor synaptonuclear signaling and neuronal migration factor
OCRL oculocerebrorenal syndrome of Lowe
P4HB prolyl 4-hydroxylase, beta polypeptide
PLXND1 plexin D1
POMGNT1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
POMT1 protein-O-mannosyltransferase 1
POMT2 protein-O-mannosyltransferase 2
PROK2 prokineticin 2
PROKR2 prokineticin receptor 2
PTPN11 protein tyrosine phosphatase, non-receptor type 11
RAF1 Raf-1 proto-oncogene, serine/threonine kinase
REV3L REV3-like, polymerase (DNA directed), zeta, catalytic subunit
RNF6 ring finger protein (C3H2C3 type) 6
SCN4A sodium channel, voltage gated, type IV alpha subunit
SEC24D SEC24 family member D
SEMA3A sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A
SH3BP2 SH3-domain binding protein 2
SIN3A SIN3 transcription regulator family member A
SLC2A3 solute carrier family 2 (facilitated glucose transporter), member 3
SMAD4 SMAD family member 4
SOX10 SRY (sex determining region Y)-box 10
SPRY4 sprouty homolog 4 (Drosophila)
SRD5A2 steroid-5-alpha-reductase, alpha polypeptide 2 (3-oxo-5 alpha-steroid delta 4-dehydrogenase alpha 2)
TAC3 tachykinin 3
TACR3 tachykinin receptor 3
TGFBR2 transforming growth factor, beta receptor II (70/80kDa)
TOR1A torsin family 1, member A (torsin A)
TP63 tumor protein p63
TSPYL1 TSPY-like 1
WDR11 WD repeat domain 11
WRN Werner syndrome, RecQ helicase-like
WWOX WW domain containing oxidoreductase