This gene encodes one of the two alpha chains of type XI collagen, a minor fibrillar collagen. It is located on chromosome 6 very close to but separate from the gene for retinoid X receptor beta. Type XI collagen is a heterotrimer but the third alpha chain is a post-translationally modified alpha 1 type II chain. Proteolytic processing of this type XI chain produces PARP, a proline/arginine-rich protein that is an amino terminal domain. Mutations in this gene are associated with type III Stickler syndrome, otospondylomegaepiphyseal dysplasia (OSMED syndrome), Weissenbacher-Zweymuller syndrome, autosomal dominant non-syndromic sensorineural type 13 deafness (DFNA13), and autosomal recessive non-syndromic sensorineural type 53 deafness (DFNB53). Alternative splicing results in multiple transcript variants. A related pseudogene is located nearby on chromosome 6. [provided by RefSeq, Jul 2009]
SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
COL11A2BA-20-REGO | 20 (40 μL) | 200 μL | Request Pricing | |
COL11A2BA-20-REGR | 20 (40 μL) | 200 μL | Request Pricing | |
COL11A2BA-20-ORGR | 20 (40 μL) | 200 μL | Request Pricing | |
COL11A2BA-20-GOGR | 20 (40 μL) | 200 μL | Request Pricing | |
COL11A2BA-20-GRRE | 20 (40 μL) | 200 μL | Request Pricing | |
COL11A2BA-20-GROR | 20 (40 μL) | 200 μL | Request Pricing | |
COL11A2BA-20-GRGO | 20 (40 μL) | 200 μL | Request Pricing | |
COL11A2BA-20-AQOR | 20 (40 μL) | 200 μL | Request Pricing |
This gene encodes one of the two alpha chains of type XI collagen, a minor fibrillar collagen. It is located on chromosome 6 very close to but separate from the gene for retinoid X receptor beta. Type XI collagen is a heterotrimer but the third alpha chain is a post-translationally modified alpha 1 type II chain. Proteolytic processing of this type XI chain produces PARP, a proline/arginine-rich protein that is an amino terminal domain. Mutations in this gene are associated with type III Stickler syndrome, otospondylomegaepiphyseal dysplasia (OSMED syndrome), Weissenbacher-Zweymuller syndrome, autosomal dominant non-syndromic sensorineural type 13 deafness (DFNA13), and autosomal recessive non-syndromic sensorineural type 53 deafness (DFNB53). Alternative splicing results in multiple transcript variants. A related pseudogene is located nearby on chromosome 6. [provided by RefSeq, Jul 2009]
Gene Symbol : COL11A2
Gene Name : Collagen type XI alpha 2 chain
Chromosome : CHR 6: 331,930,08-331,626,91
Locus : 6p21.32
Alt. Genes : PDZK1IP1
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