Gene Ontology annotation through association of InterPro records with GO terms

Annotation inferences using phylogenetic trees

Electronic Gene Ontology annotations created by ARBA machine learning models

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

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

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

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

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

The collagen family members as cell adhesion proteins.

Proteomic characterization of human multiple myeloma bone marrow extracellular matrix.

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

Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus.

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.

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

Gelatin degradation by MMP1, 2, 3, 7, 8, 9, 12, 13

Formation of collagen fibrils

Removal of fibrillar collagen N-propeptides

Removal of fibrillar collagen C-propeptides

Procollagen triple helix formation

Secretion of collagens

Formation of collagen fibres

Collagen XI cross-links with collagen II

Association of procollagen type XI

COL11A2 source evidence and assay-scope index