deviation of the thumb Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Displacement of the thumb from its normal position. (Human Phenotype Ontology, HP_0009603)
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24 genes associated with the deviation of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ANKRD11 ankyrin repeat domain 11
B3GALTL beta 1,3-galactosyltransferase-like
BMP4 bone morphogenetic protein 4
CHSY1 chondroitin sulfate synthase 1
DHCR7 7-dehydrocholesterol reductase
EFTUD2 elongation factor Tu GTP binding domain containing 2
EIF4A3 eukaryotic translation initiation factor 4A3
FLNA filamin A, alpha
FLNB filamin B, beta
GATA4 GATA binding protein 4
HDAC8 histone deacetylase 8
HOXA13 homeobox A13
MGAT2 mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase
NIPBL Nipped-B homolog (Drosophila)
NOG noggin
RAD21 RAD21 homolog (S. pombe)
SLC26A2 solute carrier family 26 (anion exchanger), member 2
SMC1A structural maintenance of chromosomes 1A
SMC3 structural maintenance of chromosomes 3
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
TP63 tumor protein p63
UBA1 ubiquitin-like modifier activating enzyme 1
ZC4H2 zinc finger, C4H2 domain containing
ZIC3 Zic family member 3