prominent nasolabial fold Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Exaggerated bulkiness of the crease or fold of skin running from the lateral margin of the nose, where nasal base meets the skin of the face, to a point just lateral to the corner of the mouth (cheilion, or commissure). (Human Phenotype Ontology, HP_0005272)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005272
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Genes

5 genes associated with the prominent nasolabial fold phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
MYH3 myosin, heavy chain 3, skeletal muscle, embryonic
NF1 neurofibromin 1
TNNI2 troponin I type 2 (skeletal, fast)
TNNT3 troponin T type 3 (skeletal, fast)
TPM2 tropomyosin 2 (beta)