short ribs Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Reduced rib length. (Human Phenotype Ontology, HP_0000773)
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25 gene mutations causing the short ribs phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ANO6 anoctamin 6
BMP4 bone morphogenetic protein 4
CHSY1 chondroitin sulfate synthase 1
COL2A1 collagen, type II, alpha 1
DYM dymeclin
EVC Ellis van Creveld protein
EVC2 Ellis van Creveld syndrome 2
FGFR3 fibroblast growth factor receptor 3
HOXA10 homeobox A10
HOXC10 homeobox C10
HOXC4 homeobox C4
IHH indian hedgehog
IMPAD1 inositol monophosphatase domain containing 1
MYF5 myogenic factor 5
MYF6 myogenic factor 6 (herculin)
MYOG myogenin (myogenic factor 4)
POSTN periostin, osteoblast specific factor
PTHLH parathyroid hormone-like hormone
SIK3 SIK family kinase 3
SMPD3 sphingomyelin phosphodiesterase 3, neutral membrane (neutral sphingomyelinase II)
SOX5 SRY (sex determining region Y)-box 5
T T, brachyury homolog (mouse)
WDR19 WD repeat domain 19
WDR35 WD repeat domain 35
XYLT1 xylosyltransferase I