This gene encodes a mitochondrially localized protein that is highly conserved across species. The gene is expressed in a variety of tissues including human lymphoblast cells and rat neurosensorial epithelium of the cristaampullaris. A mutation in this gene has been associated with familial Meniere's disease, a chronic disorder of the inner ear. Several pseudogenes of this gene are found on other chromosomes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2016]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| FAM136A-20-RE | 20 (40 μL) | 200 μL |  |
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| FAM136A-20-OR | 20 (40 μL) | 200 μL |  |
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| FAM136A-20-GO | 20 (40 μL) | 200 μL |  |
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| FAM136A-20-GR | 20 (40 μL) | 200 μL |  |
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| FAM136A-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a mitochondrially localized protein that is highly conserved across species. The gene is expressed in a variety of tissues including human lymphoblast cells and rat neurosensorial epithelium of the cristaampullaris. A mutation in this gene has been associated with familial Meniere's disease, a chronic disorder of the inner ear. Several pseudogenes of this gene are found on other chromosomes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2016]
Gene Symbol : FAM136A
Gene Name : Family with sequence similarity 136 member A
Chromosome : CHR 2: 703,020,87-702,959,75
Locus : 2p13.3
Alt. Genes : YAF2
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