abnormal scapula morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of either or both of the large, flat bones of the back part of the shoulder (Mammalian Phenotype Ontology, MP_0000149)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000149
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Genes

29 gene mutations causing the abnormal scapula morphology 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
CBFB core-binding factor, beta subunit
CBX2 chromobox homolog 2
CHST11 carbohydrate (chondroitin 4) sulfotransferase 11
FGF10 fibroblast growth factor 10
FGFR2 fibroblast growth factor receptor 2
FOXC1 forkhead box C1
HAPLN1 hyaluronan and proteoglycan link protein 1
HECTD2 HECT domain containing E3 ubiquitin protein ligase 2
HOXB5 homeobox B5
IHH indian hedgehog
IMPAD1 inositol monophosphatase domain containing 1
LMNA lamin A/C
LMX1B LIM homeobox transcription factor 1, beta
NABP2 nucleic acid binding protein 2
NPR2 natriuretic peptide receptor 2
PAX1 paired box 1
PBX1 pre-B-cell leukemia homeobox 1
PDGFRA platelet-derived growth factor receptor, alpha polypeptide
PDS5B PDS5 cohesin associated factor B
POSTN periostin, osteoblast specific factor
PTCH1 patched 1
SMPD3 sphingomyelin phosphodiesterase 3, neutral membrane (neutral sphingomyelinase II)
SOX9 SRY (sex determining region Y)-box 9
TBX15 T-box 15
TRAM2 translocation associated membrane protein 2
WNT7A wingless-type MMTV integration site family, member 7A
ZEB1 zinc finger E-box binding homeobox 1