heat shock protein family B (small), member 11
Homozygous null mice show fetal growth retardation and complete neonatal death due to severe structural heart defects. Omphalocele, polydactyly, left pulmonary isomerism, and skeletal defects such as micrognathia, cleft palate, malaligned sternal vertebrae, and a small rib cage are often observed.
|VEGA Gene Model||OTTMUSG00000008694 (Evidence)|
|Ensembl Gene Model||ENSMUSG00000063172 (Evidence)|
|Entrez Gene||72938 (Evidence)|
|DoTS||DT.101312845, DT.529270, DT.91347823, DT.97342135|
|NIA Mouse Gene Index||U004601|
|Consensus CDS Project||CCDS18435.1|
|International Mouse Knockout Project Status||Hspb11|
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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