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FAM161A
family with sequence similarity 161, member A
FAM161A 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.
| Gene Name: | family with sequence similarity 161, member A |
| Synonyms: | FAM161A, Protein FAM161A, RP28 |
| Target Sequences: | AK023367 BAB14544.1 Q3B820 |
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