Sequence Detail

ID/Version

Q811W2 Q3TM12 (UniProt | EBI)

Last sequence update: 2003-06-01
Last annotation update: 2024-11-27

Sequence description from provider

RecName: Full=Cytochrome P450 26B1; EC=1.14.13.- {ECO:0000250|UniProtKB:Q9NR63};AltName: Full=Cytochrome P450 retinoic acid-inactivating 2; Short=Cytochrome P450RAI-2;

Provider

SWISS-PROT

Sequence

Polypeptide 512 aa

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	Cyp26b1	cytochrome P450, family 26, subfamily b, polypeptide 1	47	153	3	19

Sequence references in MGI

J:81347 Menke DB, et al., Sexually dimorphic gene expression in the developing mouse gonad. Gene Expr Patterns. 2002 Dec;2(3-4):359-67
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:107319 Koubova J, et al., Retinoic acid regulates sex-specific timing of meiotic initiation in mice. Proc Natl Acad Sci U S A. 2006 Feb 21;103(8):2474-9
J:108333 Bowles J, et al., Retinoid signaling determines germ cell fate in mice. Science. 2006 Apr 28;312(5773):596-600
J:154048 Li H, et al., Cyp26b1 expression in murine Sertoli cells is required to maintain male germ cells in an undifferentiated state during embryogenesis. PLoS One. 2009;4(10):e7501
J:191406 Laue K, et al., Craniosynostosis and multiple skeletal anomalies in humans and zebrafish result from a defect in the localized degradation of retinoic acid. Am J Hum Genet. 2011 Nov 11;89(5):595-606