Sequence Detail

ID/Version

P28481 Q6LDI9 Q6LDB1 Q62031 Q62032 Q80X38 Q80VY3 Q8CEF7 Q61428 Q641K3 Q8K0N6 Q62033 Q6LDI8 (UniProt | EBI)

Last sequence update: 2007-02-06
Last annotation update: 2024-03-27

Sequence description from provider

RecName: Full=Collagen alpha-1(II) chain {ECO:0000250|UniProtKB:P02458};AltName: Full=Alpha-1 type II collagen {ECO:0000250|UniProtKB:P02458};Contains: RecName: Full=Collagen alpha-1(II) chain {ECO:0000250|UniProtKB:P02458};Contains: RecName: Full=Chond

Provider

SWISS-PROT

Sequence

Polypeptide 1487 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	Col2a1	collagen, type II, alpha 1	71	354	4	31

Sequence references in MGI

J:11264 Metsaranta M, et al., Specific hybridization probes for mouse type I, II, III and IX collagen mRNAs. Biochim Biophys Acta. 1991 Jun 13;1089(2):241-3
J:11400 Metsaranta M, et al., Mouse type II collagen gene. Complete nucleotide sequence, exon structure, and alternative splicing. J Biol Chem. 1991 Sep 5;266(25):16862-9
J:11632 Cheah KSE, et al., The mouse Col2a-1 gene is highly conserved and is linked to Int-1 on chromosome 15. Mamm Genome. 1991;1(3):171-83
J:32246 Cheah KS, et al., Expression of the mouse alpha 1(II) collagen gene is not restricted to cartilage during development. Development. 1991 Apr;111(4):945-53
J:85735 Donahue LR, et al., A missense mutation in the mouse Col2a1 gene causes spondyloepiphyseal dysplasia congenita, hearing loss, and retinoschisis. J Bone Miner Res. 2003 Sep;18(9):1612-21
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