COL11A2 Break Apart FISH Probe

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 Details
SKU Test Kits Buffer Dye Color Order Now
COL11A2BA-20-REGO 20 (40 μL) 200 μL color color Request Pricing
COL11A2BA-20-REGR 20 (40 μL) 200 μL color color Request Pricing
COL11A2BA-20-ORGR 20 (40 μL) 200 μL color color Request Pricing
COL11A2BA-20-GOGR 20 (40 μL) 200 μL color color Request Pricing
COL11A2BA-20-GRRE 20 (40 μL) 200 μL color color Request Pricing
COL11A2BA-20-GROR 20 (40 μL) 200 μL color color Request Pricing
COL11A2BA-20-GRGO 20 (40 μL) 200 μL color color Request Pricing
COL11A2BA-20-AQOR 20 (40 μL) 200 μL color color Request Pricing

Gene Summary

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 Details

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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