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FAM161A


Official Full Name
FAM161 centrosomal protein A
Organism
Homo sapiens
Gene ID
84140
Background
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]
Synonyms
RP28

Cat.No. Product Name Price
SHH289929 shRNA set against Mouse FAM161A (NM_028672.2) Inquiry
SHH289933 shRNA set against Rat FAM161A (NM_001013876.2) Inquiry
Cat.No. Product Name Price
CDCB185966 Rabbit FAM161A ORF clone (XM_008254359.1) Inquiry
CDCS409556 Human FAM161A ORF Clone (BC107163) Inquiry
CDFR002955 Rat Fam161a cDNA Clone(NM_001013876.2) Inquiry
CDCG001842 Mouse FAM161A ORF clone(NM_028672.2) Inquiry
CDCR370044 Rat Fam161a ORF Clone(NM_001013876.2) Inquiry
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