This gene belongs to the FAM161 family. It is expressed mainly in the retina. Mouse studies suggested that this gene is involved in development of retinal progenitors during embryogenesis, and that its activity is restricted to mature photoreceptors after birth. Mutations in this gene cause autosomal recessive retinitis pigmentosa-28. Alternatively spliced transcript variants have been identified.[provided by RefSeq, Jan 2011]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| FAM161A-20-RE | 20 (40 μL) | 200 μL |  |
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| FAM161A-20-OR | 20 (40 μL) | 200 μL |  |
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| FAM161A-20-GO | 20 (40 μL) | 200 μL |  |
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| FAM161A-20-GR | 20 (40 μL) | 200 μL |  |
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| FAM161A-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene belongs to the FAM161 family. It is expressed mainly in the retina. Mouse studies suggested that this gene is involved in development of retinal progenitors during embryogenesis, and that its activity is restricted to mature photoreceptors after birth. Mutations in this gene cause autosomal recessive retinitis pigmentosa-28. Alternatively spliced transcript variants have been identified.[provided by RefSeq, Jan 2011]
Gene Symbol : FAM161A
Gene Name : Family with sequence similarity 161 member A
Chromosome : CHR 2: 618,560,73-618,002,39
Locus : 2p15
Alt. Genes : RAD50
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