absent phalangeal crease Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence of one or more interphalangeal creases (i.e., of the transverse lines in the skin between the phalanges of the fingers). (Human Phenotype Ontology, HP_0006109)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006109
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Genes

12 genes associated with the absent phalangeal crease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
HOXD13 homeobox D13
IHH indian hedgehog
LMX1B LIM homeobox transcription factor 1, beta
MASP1 mannan-binding lectin serine peptidase 1 (C4/C2 activating component of Ra-reactive factor)
MYH3 myosin, heavy chain 3, skeletal muscle, embryonic
NOG noggin
PIEZO2 piezo-type mechanosensitive ion channel component 2
RBBP8 retinoblastoma binding protein 8
TBX15 T-box 15
TNNI2 troponin I type 2 (skeletal, fast)
TNNT3 troponin T type 3 (skeletal, fast)
TPM2 tropomyosin 2 (beta)