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Symbol Name ID |
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| Synonyms | Cavbeta2, Cchb2 | |||||||||||||||||||||
| Feature Type | protein coding gene | |||||||||||||||||||||
| Genetic Map | ||||||||||||||||||||||
| Sequence Map |
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Vertebrate homology |
HomoloGene:75191 Vertebrate Homology Class 1 human; 1 mouse; 1 rat; 1 chimpanzee; 1 rhesus macaque; 1 cattle; 1 dog; 1 chicken; 1 zebrafish Gene Tree: Cacnb2 |
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| Human homologs |
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Alleles and phenotypes |
All alleles(6) :
Targeted(6)
Mice homozygous for a null allele exhibit lethality at E10.5 with growth retardation, abnormal yolk vasculature and abnormal cardiac development and function. |
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Gene Ontology (GO) classifications |
All GO classifications: (28 annotations)
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| Expression |
Literature Summary: (9 records) Data Summary: Results (94) Tissues (51) Images (20) Theiler Stages: 15, 17, 20, 23, 24, 25, 26, 28
External Resources: Allen Institute GEO ArrayExpress |
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Molecular reagents |
All nucleic(24)
cDNA(21)
Primer pair(2)
Other(1)
Microarray probesets(5) |
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Other database links |
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| Sequences |
All sequences(66) RefSeq(5) UniProt(8) |
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| Polymorphisms | RFLP(2) : SNPs(1123 from dbSNP Build 128) | |||||||||||||||||||||
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Protein-related information |
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| References |
(Earliest) J:25718
Massa E, et al., Comparison of fura-2 imaging and electrophysiological analysis of murine calcium channel alpha 1 subunits coexpressed with novel beta 2 subunit isoforms. Mol Pharmacol. 1995 Apr;47(4):707-16 (Latest) J:193641 Nakano Y, et al., A mutation in the Srrm4 gene causes alternative splicing defects and deafness in the Bronx waltzer mouse. PLoS Genet. 2012;8(10):e1002966 All references(60) |
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Other accession IDs |
MGD-MRK-24068, MGI:103200, MGI:2139283, MGI:3583767 |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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