truncal obesity Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Obesity located preferentially in the trunk of the body as opposed to the extremities. (Human Phenotype Ontology, HP_0001956)
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25 genes associated with the truncal obesity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AKT2 v-akt murine thymoma viral oncogene homolog 2
ALMS1 Alstrom syndrome protein 1
ARMC5 armadillo repeat containing 5
CREBBP CREB binding protein
CUL4B cullin 4B
DYRK1B dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1B
FMR1 fragile X mental retardation 1
GHR growth hormone receptor
GNAS GNAS complex locus
HDAC8 histone deacetylase 8
INPP5E inositol polyphosphate-5-phosphatase, 72 kDa
NIPBL Nipped-B homolog (Drosophila)
PCNT pericentrin
PDE11A phosphodiesterase 11A
PDE8B phosphodiesterase 8B
PHF6 PHD finger protein 6
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha
RAD21 RAD21 homolog (S. pombe)
SLC7A7 solute carrier family 7 (amino acid transporter light chain, y+L system), member 7
SMC1A structural maintenance of chromosomes 1A
SMC3 structural maintenance of chromosomes 3
TRAPPC9 trafficking protein particle complex 9
VPS13B vacuolar protein sorting 13 homolog B (yeast)
XYLT1 xylosyltransferase I
ZBTB20 zinc finger and BTB domain containing 20