decreased body height Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A height below that which is expected according to age and gender norms. Although there is no universally accepted definition of short stature, many refer to short stature as height more than 2 standard deviations below the mean for age and gender (or below the 3rd percentile for age and gender dependent norms). (Human Phenotype Ontology, HP_0004322)
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19 gene mutations causing the decreased body height phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACP2 acid phosphatase 2, lysosomal
CTSK cathepsin K
DLL1 delta-like 1 (Drosophila)
DNM3OS DNM3 opposite strand/antisense RNA
ERP44 endoplasmic reticulum protein 44
FGFRL1 fibroblast growth factor receptor-like 1
HERC1 HECT and RLD domain containing E3 ubiquitin protein ligase family member 1
IHH indian hedgehog
LMNA lamin A/C
LPAR1 lysophosphatidic acid receptor 1
LRRK1 leucine-rich repeat kinase 1
MED1 mediator complex subunit 1
MGP matrix Gla protein
MIR140 microRNA 140
NKX3-2 NK3 homeobox 2
NPPC natriuretic peptide C
SMPD3 sphingomyelin phosphodiesterase 3, neutral membrane (neutral sphingomyelinase II)
TGFB1 transforming growth factor, beta 1
WWTR1 WW domain containing transcription regulator 1