Collagen type XI alpha 2 chain (Q21109884)

Laminin G domain, protein family

1 reference

based on heuristic

inferred from protein domain or family

Fibrillar collagen, C-terminal domain, protein family

1 reference

based on heuristic

inferred from protein domain or family

collagen triple helix repeat, protein family

1 reference

based on heuristic

inferred from protein domain or family

1 reference

13 November 2019

1 reference

13 November 2019

protein-macromolecule adaptor activity

1 reference

8 April 2019

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

extracellular matrix structural constituent

NAS

1 reference

24 April 2018

http://www.ebi.ac.uk/QuickGO/annotations?protein=P13942&geneProductId=UniProtKB:P13942

1 reference

8 April 2019

Structural basis of the collagen-binding mode of discoidin domain receptor 2

IntAct protein interaction database

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942

extracellular matrix structural constituent conferring tensile strength

IPI

2 references

24 April 2018

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

24 April 2018

Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus

http://www.ebi.ac.uk/QuickGO/annotations?protein=P13942&geneProductId=UniProtKB:P13942

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942

extracellular matrix structural constituent conferring tensile strength

IEA

4 references

1 January 2018

Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus

http://www.ebi.ac.uk/QuickGO/annotations?protein=P13942&geneProductId=UniProtKB:P13942

1 January 2018

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

1 January 2018

Proteomic characterization of human multiple myeloma bone marrow extracellular matrix.

http://www.ebi.ac.uk/QuickGO/annotations?protein=P13942&geneProductId=UniProtKB:P13942

1 January 2018

Characterization of the Extracellular Matrix of Normal and Diseased Tissues Using Proteomics.

http://www.ebi.ac.uk/QuickGO/annotations?protein=P13942&geneProductId=UniProtKB:P13942

extracellular matrix structural constituent conferring tensile strength

HDA

6 references

1 January 2018

Proteomic characterization of human multiple myeloma bone marrow extracellular matrix.

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942

1 January 2018

Characterization of the Extracellular Matrix of Normal and Diseased Tissues Using Proteomics.

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942

1 January 2018

Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942

1 January 2018

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

1 January 2018

Proteomic characterization of human multiple myeloma bone marrow extracellular matrix.

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942

1 January 2018

Characterization of the Extracellular Matrix of Normal and Diseased Tissues Using Proteomics.

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942

extracellular matrix structural constituent conferring tensile strength

IEA

4 references

8 April 2019

Characterization of the Extracellular Matrix of Normal and Diseased Tissues Using Proteomics.

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942

8 April 2019

Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942

8 April 2019

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

8 April 2019

Proteomic characterization of human multiple myeloma bone marrow extracellular matrix.

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942

1 reference

24 April 2018

http://www.ebi.ac.uk/QuickGO/annotations?protein=P13942&geneProductId=UniProtKB:P13942

endoplasmic reticulum lumen

IEA

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942

Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus

TAS

collagen type XI trimer

2 references

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942

8 April 2019

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

1 reference

8 April 2019

Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942

1 reference

8 April 2019

Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942

Autosomal recessive disorder otospondylomegaepiphyseal dysplasia is associated with loss-of-function mutations in the COL11A2 gene

biological process

soft palate development

1 reference

8 April 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942

skeletal system development

3 references

8 April 2019

Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942

8 April 2019

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

8 April 2019

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

roof of mouth development

1 reference

8 April 2019

Collagen XI sequence variations in nonsyndromic cleft palate, Robin sequence and micrognathia

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942

Oto- spondylo-megaepiphyseal dysplasia (OSMED): clinical description of three patients homozygous for a missense mutation in the COL11A2 gene

cartilage development

1 reference

24 April 2018

http://www.ebi.ac.uk/QuickGO/annotations?protein=P13942&geneProductId=UniProtKB:P13942

4 references

24 April 2018

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

24 April 2018

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

24 April 2018

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

24 April 2018

Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)

Mouse Genome Informatics

http://www.ebi.ac.uk/QuickGO/annotations?protein=P13942&geneProductId=UniProtKB:P13942

collagen fibril organization

1 reference

24 April 2018

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

5 references

8 April 2019

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

8 April 2019

Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locus

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942

8 April 2019

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

8 April 2019

Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)

Mouse Genome Informatics

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942

8 April 2019

Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942

extracellular matrix organization

1 reference

8 April 2019

Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P13942

collagen fibril organization

Fibrillar collagen, C-terminal

IDA

cartilage development

1 reference

Laminin G domain

1 reference

Collagen triple helix repeat

1 reference