# Collagen type XI alpha 2 chain

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21109884](https://www.wikidata.org/wiki/Q21109884)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Collagen,_type_XI,_alpha_2)  
**Source**: https://4ort.xyz/entity/collagen-type-xi-alpha-2-chain


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/P13942)
3. Q20641742
4. [Autosomal recessive disorder otospondylomegaepiphyseal dysplasia is associated with loss-of-function mutations in the COL11A2 gene](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942)
5. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=P13942&geneProductId=UniProtKB:P13942)
6. [Structural basis of the collagen-binding mode of discoidin domain receptor 2](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942)
7. [The human alpha 2(XI) collagen gene (COL11A2): completion of coding information, identification of the promoter sequence, and precise localization within the major histocompatibility complex reveal overlap with the KE5 gene](http://www.ebi.ac.uk/QuickGO/annotations?protein=P13942&geneProductId=UniProtKB:P13942)
8. [Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus](http://www.ebi.ac.uk/QuickGO/annotations?protein=P13942&geneProductId=UniProtKB:P13942)
9. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942)
10. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942)
11. [Proteomic characterization of human multiple myeloma bone marrow extracellular matrix.](http://www.ebi.ac.uk/QuickGO/annotations?protein=P13942&geneProductId=UniProtKB:P13942)
12. [Characterization of the Extracellular Matrix of Normal and Diseased Tissues Using Proteomics.](http://www.ebi.ac.uk/QuickGO/annotations?protein=P13942&geneProductId=UniProtKB:P13942)
13. [Proteomic characterization of human multiple myeloma bone marrow extracellular matrix.](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942)
14. [Characterization of the Extracellular Matrix of Normal and Diseased Tissues Using Proteomics.](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942)
15. [Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942)
16. [The human alpha 2(XI) collagen gene (COL11A2): completion of coding information, identification of the promoter sequence, and precise localization within the major histocompatibility complex reveal overlap with the KE5 gene](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942)
17. [Collagen XI sequence variations in nonsyndromic cleft palate, Robin sequence and micrognathia](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942)
18. [Oto- spondylo-megaepiphyseal dysplasia (OSMED): clinical description of three patients homozygous for a missense mutation in the COL11A2 gene](http://www.ebi.ac.uk/QuickGO/annotations?protein=P13942&geneProductId=UniProtKB:P13942)
19. [Autosomal recessive disorder otospondylomegaepiphyseal dysplasia is associated with loss-of-function mutations in the COL11A2 gene](http://www.ebi.ac.uk/QuickGO/annotations?protein=P13942&geneProductId=UniProtKB:P13942)
20. [Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locus](http://www.ebi.ac.uk/QuickGO/annotations?protein=P13942&geneProductId=UniProtKB:P13942)
21. [Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)](http://www.ebi.ac.uk/QuickGO/annotations?protein=P13942&geneProductId=UniProtKB:P13942)
22. [Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locus](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942)
23. [Oto- spondylo-megaepiphyseal dysplasia (OSMED): clinical description of three patients homozygous for a missense mutation in the COL11A2 gene](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942)
24. [Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942)
25. [Identifiers.org](https://registry.identifiers.org/registry/uniprot)