This gene encodes a member of the ATPase associated with diverse activities family, whose members are defined by a highly conserved ATPase domain. Members of this family participate in diverse cellular processes that include membrane fusion, DNA replication, microtubule severing, and protein degradation. The protein encoded by this gene has a putative mitochondrial targeting sequence and has been proposed to function in maintenance of mitochondrial function and integrity during mouse spermatogenesis. Allelic variants in this gene have been associated with epilepsy, hearing loss, and cognitive disability syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]
SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
SPATA5-20-RE | 20 (40 μL) | 200 μL | ![]() |
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SPATA5-20-OR | 20 (40 μL) | 200 μL | ![]() |
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SPATA5-20-GO | 20 (40 μL) | 200 μL | ![]() |
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SPATA5-20-GR | 20 (40 μL) | 200 μL | ![]() |
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SPATA5-20-AQ | 20 (40 μL) | 200 μL | ![]() |
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This gene encodes a member of the ATPase associated with diverse activities family, whose members are defined by a highly conserved ATPase domain. Members of this family participate in diverse cellular processes that include membrane fusion, DNA replication, microtubule severing, and protein degradation. The protein encoded by this gene has a putative mitochondrial targeting sequence and has been proposed to function in maintenance of mitochondrial function and integrity during mouse spermatogenesis. Allelic variants in this gene have been associated with epilepsy, hearing loss, and cognitive disability syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]
Gene Symbol : SPATA5
Gene Name : Spermatogenesis associated 5
Chromosome : CHR 4: 122,923,069-123,319,449
Locus : 4q28.1
Alt. Genes : SGK2
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