CA8 Break Apart FISH Probe

The protein encoded by this gene was initially named CA-related protein because of sequence similarity to other known carbonic anhydrase genes. However, the gene product lacks carbonic anhydrase activity (i.e., the reversible hydration of carbon dioxide). The gene product continues to carry a carbonic anhydrase designation based on clear sequence identity to other members of the carbonic anhydrase gene family. The absence of CA8 gene transcription in the cerebellum of the lurcher mutant in mice with a neurologic defect suggests an important role for this acatalytic form. Mutations in this gene are associated with cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 (CMARQ3). Polymorphisms in this gene are associated with osteoporosis, and overexpression of this gene in osteosarcoma cells suggests an oncogenic role. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]


Gene Details
SKU Test Kits Buffer Dye Color Order Now
CA8BA-20-REGO 20 (40 μL) 200 μL color color Request Pricing
CA8BA-20-REGR 20 (40 μL) 200 μL color color Request Pricing
CA8BA-20-ORGR 20 (40 μL) 200 μL color color Request Pricing
CA8BA-20-GOGR 20 (40 μL) 200 μL color color Request Pricing
CA8BA-20-GRRE 20 (40 μL) 200 μL color color Request Pricing
CA8BA-20-GROR 20 (40 μL) 200 μL color color Request Pricing
CA8BA-20-GRGO 20 (40 μL) 200 μL color color Request Pricing
CA8BA-20-AQOR 20 (40 μL) 200 μL color color Request Pricing

Gene Summary

The protein encoded by this gene was initially named CA-related protein because of sequence similarity to other known carbonic anhydrase genes. However, the gene product lacks carbonic anhydrase activity (i.e., the reversible hydration of carbon dioxide). The gene product continues to carry a carbonic anhydrase designation based on clear sequence identity to other members of the carbonic anhydrase gene family. The absence of CA8 gene transcription in the cerebellum of the lurcher mutant in mice with a neurologic defect suggests an important role for this acatalytic form. Mutations in this gene are associated with cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 (CMARQ3). Polymorphisms in this gene are associated with osteoporosis, and overexpression of this gene in osteosarcoma cells suggests an oncogenic role. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]

Gene Details

Gene Symbol : CA8

Gene Name : Carbonic anhydrase 8

Chromosome : CHR 8: 602,814,22-601,854,19

Locus : 8q12.1

Alt. Genes : OPTN

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