bifid tongue Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Tongue with a median apical indentation or fork. (Human Phenotype Ontology, HP_0010297)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010297
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Genes

13 genes associated with the bifid tongue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
C5ORF42 chromosome 5 open reading frame 42
DHCR7 7-dehydrocholesterol reductase
DYNC2H1 dynein, cytoplasmic 2, heavy chain 1
FRAS1 Fraser extracellular matrix complex subunit 1
FREM2 FRAS1 related extracellular matrix protein 2
GRIP1 glutamate receptor interacting protein 1
KIF7 kinesin family member 7
OFD1 oral-facial-digital syndrome 1
PDE6D phosphodiesterase 6D, cGMP-specific, rod, delta
ROR2 receptor tyrosine kinase-like orphan receptor 2
TCTN3 tectonic family member 3
TMEM216 transmembrane protein 216
WNT5A wingless-type MMTV integration site family, member 5A