protruding tongue Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Tongue extending beyond the alveolar ridges or teeth at rest. (Human Phenotype Ontology, HP_0010808)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010808
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Genes

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

Symbol Name
ATRX alpha thalassemia/mental retardation syndrome X-linked
CDKL5 cyclin-dependent kinase-like 5
CHUK conserved helix-loop-helix ubiquitous kinase
DNMT3B DNA (cytosine-5-)-methyltransferase 3 beta
EHMT1 euchromatic histone-lysine N-methyltransferase 1
FAM20C family with sequence similarity 20, member C
FTO fat mass and obesity associated
GATA1 GATA binding protein 1 (globin transcription factor 1)
INPP5E inositol polyphosphate-5-phosphatase, 72 kDa
MECP2 methyl CpG binding protein 2
MGAT2 mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase
NRXN1 neurexin 1
PEX1 peroxisomal biogenesis factor 1
UBE3A ubiquitin protein ligase E3A