small scapula Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Underdeveloped scapula. (Human Phenotype Ontology, HP_0000882)
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15 gene mutations causing the small scapula phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BMPER BMP binding endothelial regulator
CACNA1S calcium channel, voltage-dependent, L type, alpha 1S subunit
CHST11 carbohydrate (chondroitin 4) sulfotransferase 11
FGFR2 fibroblast growth factor receptor 2
HAPLN1 hyaluronan and proteoglycan link protein 1
IHH indian hedgehog
IMPAD1 inositol monophosphatase domain containing 1
LMX1B LIM homeobox transcription factor 1, beta
NABP2 nucleic acid binding protein 2
NPR2 natriuretic peptide receptor 2
PDS5B PDS5 cohesin associated factor B
POSTN periostin, osteoblast specific factor
SOX9 SRY (sex determining region Y)-box 9
TBX15 T-box 15
ZEB1 zinc finger E-box binding homeobox 1