abnormal compact bone volume Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the amount of space occupied by compact bone tissue in the skeleton (Mammalian Phenotype Ontology, MP_0010963)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010963
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9 gene mutations causing the abnormal compact bone volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
GALNT3 polypeptide N-acetylgalactosaminyltransferase 3
GATA1 GATA binding protein 1 (globin transcription factor 1)
GSK3B glycogen synthase kinase 3 beta
IGHM immunoglobulin heavy constant mu
JAK1 Janus kinase 1
POSTN periostin, osteoblast specific factor
PRDM5 PR domain containing 5
SOST sclerostin
STAT1 signal transducer and activator of transcription 1, 91kDa