overgrowth Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Excessive postnatal growth which may comprise increased weight, increased length, and/or increased head circumference. (Human Phenotype Ontology, HP_0001548)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001548
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Genes

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

Symbol Name
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
EFEMP2 EGF containing fibulin-like extracellular matrix protein 2
FAM20A family with sequence similarity 20, member A
FBN1 fibrillin 1
H19 H19, imprinted maternally expressed transcript (non-protein coding)
HRAS Harvey rat sarcoma viral oncogene homolog
HSPG2 heparan sulfate proteoglycan 2
KCNQ1OT1 KCNQ1 opposite strand/antisense transcript 1 (non-protein coding)
KRAS Kirsten rat sarcoma viral oncogene homolog
NF1 neurofibromin 1
NFIX nuclear factor I/X (CCAAT-binding transcription factor)
NSD1 nuclear receptor binding SET domain protein 1
PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
SOST sclerostin