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Sequence Detail
ID/Version
Q922I5 Q9D299 Q5SRI5 (UniProt | EBI) Last sequence update: 2007-06-26
Last annotation update: 2024-01-24
Sequence
description
from provider
RecName: Full=Forkhead box protein I1;
Provider SWISS-PROT
Sequence
Polypeptide 372 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 Foxi1 forkhead box I1 22 109 5 6
Sequence references in MGI J:82307 Hulander M, et al., Lack of pendrin expression leads to deafness and expansion of the endolymphatic compartment in inner ears of Foxi1 null mutant mice. Development. 2003 May;130(9):2013-25
J:90907 Blomqvist SR, et al., Distal renal tubular acidosis in mice that lack the forkhead transcription factor Foxi1. J Clin Invest. 2004 Jun;113(11):1560-70
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

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
04/16/2024
MGI 6.23
The Jackson Laboratory