collagen alpha-2(IX) chain isoform X2 [Homo sapiens]

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View conserved domains detected in this protein sequence using CD-search.

Autosomal recessive Stickler syndrome associated with homozygous mutations in the COL9A2 gene. [Ophthalmic Genet. 2021]
Autosomal recessive Stickler syndrome associated with homozygous mutations in the COL9A2 gene.
Kjellström U, Martell S, Brobeck C, Andréasson S. Ophthalmic Genet. 2021 Apr; 42(2):161-169. Epub 2020 Dec 27.
Association between COL9A2 Gln326Arg mutations and the development of intervertebral disc disease in a Chinese population. [Genet Mol Res. 2016]
Association between COL9A2 Gln326Arg mutations and the development of intervertebral disc disease in a Chinese population.
Meng T, Ren Q, Wang JM, Shi H, Zhang ST, Liu MT. Genet Mol Res. 2016 Dec 19; 15(4). Epub 2016 Dec 19.
Meta-analysis of the association between COL9A2 genetic polymorphisms and lumbar disc disease susceptibility. [Spine (Phila Pa 1976). 2014]
Meta-analysis of the association between COL9A2 genetic polymorphisms and lumbar disc disease susceptibility.
Zhang Z, Zhang J, Ding L, Teng X. Spine (Phila Pa 1976). 2014 Sep 15; 39(20):1699-706.

RefSeq genomic sequence
See the genomic reference sequence for the COL9A2 gene (NG_008031.1).
RefSeq mRNA
See reference mRNA sequence for the COL9A2 gene (XM_054334469.1).

Cribbea gloriosa voucher MEL2313432 internal transcribed spacer 1, partial seque...
Cribbea gloriosa voucher MEL2313432 internal transcribed spacer 1, partial sequence; 5.8S ribosomal RNA gene, complete sequence; and internal transcribed spacer 2, partial sequence
gi|223929990|gb|FJ178108.1|

Nucleotide
Agaricus tephrolepidus translation elongation factor 1-alpha (tef1) gene, partia...
Agaricus tephrolepidus translation elongation factor 1-alpha (tef1) gene, partial cds.
PopSet: 2654366041

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Protein