ID/Version |
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Sequence description from provider |
RecName: Full=Spectrin beta chain, non-erythrocytic 1;AltName: Full=Beta-II spectrin;AltName: Full=Embryonic liver fodrin;AltName: Full=Fodrin beta chain; | ||||||||||||||
Provider | SWISS-PROT | ||||||||||||||
Sequence |
Polypeptide
2363
aa
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Source | |||||||||||||||
Annotated genes and markers |
Follow the symbol links to get more information on the GO terms,
expression assays, orthologs, phenotypic alleles, and other information
for the genes or markers below.
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Sequence references in MGI |
J:43410
Ma Y, et al., The complete amino acid sequence for brain beta spectrin (beta fodrin): relationship to globin sequences [published errata appear in Brain Res Mol Brain Res 1993 Oct;20(1-2):179 and 1994 Jan;21(1-2):181 and 1995 May;30(1):176]. Brain Res Mol Brain Res. 1993 Apr;18(1-2):87-99
J:52539 Mishra L, et al., Elf3 encodes a novel 200-kD beta-spectrin: role in liver development. Oncogene. 1999 Jan 14;18(2):353-64 J:93347 Mohler PJ, et al., Ankyrin-B targets beta2-spectrin to an intracellular compartment in neonatal cardiomyocytes. J Biol Chem. 2004 Oct 17;279(38):40185-93 J:99680 The FANTOM Consortium and RIKEN Genome Exploration Research Group and Genome Science Group (Genome Network Project Core Group), The Transcriptional Landscape of the Mammalian Genome. Science. 2005;309(5740):1559-1563 J:177167 Tomsig JL, et al., Identification of targets for calcium signaling through the copine family of proteins. Characterization of a coiled-coil copine-binding motif. J Biol Chem. 2003 Mar 21;278(12):10048-54 J:187362 Munton RP, et al., Qualitative and quantitative analyses of protein phosphorylation in naive and stimulated mouse synaptosomal preparations. Mol Cell Proteomics. 2007 Feb;6(2):283-93 J:263376 Trinidad JC, et al., Comprehensive identification of phosphorylation sites in postsynaptic density preparations. Mol Cell Proteomics. 2006 May;5(5):914-22 J:292518 Huttlin EL, et al., A tissue-specific atlas of mouse protein phosphorylation and expression. Cell. 2010 Dec 23;143(7):1174-89 J:322307 Cousin MA, et al., Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome. Nat Genet. 2021 Jul;53(7):1006-1021 |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 03/25/2025 MGI 6.24 |
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