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Sequence Detail
ID/Version
Q61024 Q3TJA1 Q8BPC8 (UniProt | EBI) Last sequence update: 2007-01-23
Last annotation update: 2024-07-24
Sequence
description
from provider
RecName: Full=Asparagine synthetase [glutamine-hydrolyzing]; EC=6.3.5.4;AltName: Full=Glutamine-dependent asparagine synthetase;
Provider SWISS-PROT
Sequence
Polypeptide 561 aa
For this sequence
Source
Organism mouse
See UniProt | EBI for 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.
Type Symbol Name GO Terms Expression
Assays
Orthologs Phenotypic
Alleles
Gene Asns asparagine synthetase 27 106 3 19
Sequence references in MGI 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:236441 Ruzzo EK, et al., Deficiency of asparagine synthetase causes congenital microcephaly and a progressive form of encephalopathy. Neuron. 2013 Oct 16;80(2):429-41
J:292518 Huttlin EL, et al., A tissue-specific atlas of mouse protein phosphorylation and expression. Cell. 2010 Dec 23;143(7):1174-89

Contributing Projects:
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
11/12/2024
MGI 6.24
The Jackson Laboratory