Collagen, type XI, alpha 2 (Q21983048)

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

12 September 2018

1 reference

12 September 2018

1 reference

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q64739

extracellular matrix structural constituent

IEA

3 references

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q64739

14 February 2019

Collagen XI chain misassembly in cartilage of the chondrodysplasia (cho) mouse

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q64739

14 February 2019

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

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q64739

extracellular matrix structural constituent conferring tensile strength

1 reference

1 January 2018

Quantitative proteomic profiling of the extracellular matrix of pancreatic islets during the angiogenic switch and insulinoma progression.

British Heart Foundation

http://www.ebi.ac.uk/QuickGO/annotations?protein=Q64739&geneProductId=UniProtKB:Q64739

extracellular matrix structural constituent conferring tensile strength

HDA

1 reference

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q64739

3 references

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q64739

14 February 2019

Collagen XI chain misassembly in cartilage of the chondrodysplasia (cho) mouse

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q64739

14 February 2019

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

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q64739

1 reference

14 February 2019

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

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q64739

1 reference

14 February 2019

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

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q64739

collagen-containing extracellular matrix

1 reference

14 February 2019

Quantitative proteomic profiling of the extracellular matrix of pancreatic islets during the angiogenic switch and insulinoma progression.

British Heart Foundation

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q64739

HDA

biological process

soft palate development

1 reference

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q64739

skeletal system development

ISO

1 reference

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q64739

skeletal system morphogenesis

ISO

1 reference

14 February 2019

Targeted disruption of Col11a2 produces a mild cartilage phenotype in transgenic mice: comparison with the human disorder otospondylomegaepiphyseal dysplasia (OSMED)

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q64739

roof of mouth development

1 reference

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q64739

ISO

cartilage development

1 reference

24 April 2018

http://www.ebi.ac.uk/QuickGO/annotations?protein=Q64739&geneProductId=UniProtKB:Q64739

3 references

24 April 2018

http://www.ebi.ac.uk/QuickGO/annotations?protein=Q64739&geneProductId=UniProtKB:Q64739

24 April 2018

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

http://www.ebi.ac.uk/QuickGO/annotations?protein=Q64739&geneProductId=UniProtKB:Q64739

24 April 2018

Targeted disruption of Col11a2 produces a mild cartilage phenotype in transgenic mice: comparison with the human disorder otospondylomegaepiphyseal dysplasia (OSMED)

http://www.ebi.ac.uk/QuickGO/annotations?protein=Q64739&geneProductId=UniProtKB:Q64739

chondrocyte differentiation

1 reference

14 February 2019

Targeted disruption of Col11a2 produces a mild cartilage phenotype in transgenic mice: comparison with the human disorder otospondylomegaepiphyseal dysplasia (OSMED)

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q64739

1 reference

14 February 2019

More knee joint osteoarthritis (OA) in mice after inactivation of one allele of type II procollagen gene but less OA after lifelong voluntary wheel running exercise

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q64739

collagen fibril organization

3 references

24 April 2018

http://www.ebi.ac.uk/QuickGO/annotations?protein=Q64739&geneProductId=UniProtKB:Q64739

24 April 2018

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

http://www.ebi.ac.uk/QuickGO/annotations?protein=Q64739&geneProductId=UniProtKB:Q64739

24 April 2018

Targeted disruption of Col11a2 produces a mild cartilage phenotype in transgenic mice: comparison with the human disorder otospondylomegaepiphyseal dysplasia (OSMED)

http://www.ebi.ac.uk/QuickGO/annotations?protein=Q64739&geneProductId=UniProtKB:Q64739

osteoblast differentiation

1 reference

14 February 2019

Ensembl genome database project

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q64739

4 references

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q64739

14 February 2019

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

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q64739

14 February 2019

Targeted disruption of Col11a2 produces a mild cartilage phenotype in transgenic mice: comparison with the human disorder otospondylomegaepiphyseal dysplasia (OSMED)

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q64739

14 February 2019

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

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q64739

extracellular matrix organization

1 reference

14 February 2019

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

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q64739

collagen fibril organization

4 references

14 February 2019

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q64739

14 February 2019

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

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q64739

14 February 2019

Targeted disruption of Col11a2 produces a mild cartilage phenotype in transgenic mice: comparison with the human disorder otospondylomegaepiphyseal dysplasia (OSMED)

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q64739

14 February 2019

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

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q64739

Fibrillar collagen, C-terminal

has part(s)

1 reference

Collagen triple helix repeat

1 reference

Laminin G domain

1 reference