abnormal body height Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the shoulder to floor distance compared to controls (Mammalian Phenotype Ontology, MP_0001253)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001253
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Genes

19 gene mutations causing the abnormal 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