Bifid Tongue Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Tongue with a median apical indentation or fork. (Human Phenotype Ontology, HP_0010297)
External Link https://www.disgenet.org/browser/0/1/0/C0266111
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Genes

24 genes associated with the disease Bifid Tongue in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ALX3 ALX homeobox 3
C2CD3 C2 calcium-dependent domain containing 3
CEP120 centrosomal protein 120kDa
DDX59 DEAD (Asp-Glu-Ala-Asp) box polypeptide 59
DHCR7 7-dehydrocholesterol reductase
DVL1 dishevelled segment polarity protein 1
DVL3 dishevelled segment polarity protein 3
DYNC2H1 dynein, cytoplasmic 2, heavy chain 1
FLNA filamin A, alpha
FRAS1 Fraser extracellular matrix complex subunit 1
FREM2 FRAS1 related extracellular matrix protein 2
FZD2 frizzled class receptor 2
GRIP1 glutamate receptor interacting protein 1
IFT80 intraflagellar transport 80
MCTP2 multiple C2 domains, transmembrane 2
NEK1 NIMA-related kinase 1
NXN nucleoredoxin
OFD1 oral-facial-digital syndrome 1
RIPK4 receptor-interacting serine-threonine kinase 4
ROR2 receptor tyrosine kinase-like orphan receptor 2
WDR34 WD repeat domain 34
WDR35 WD repeat domain 35
WDR60 WD repeat domain 60
WNT5A wingless-type MMTV integration site family, member 5A