Family With Sequence Similarity 161, Member A (FAM161A)

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Family With Sequence Similarity 161, Member A (FAM161A)
FAM161A transcript encodes a deduced 660-amino acid protein with a calculated molecular mass of 76 kD. Alternative splicing produces a minor transcript containing an additional exon, resulting in a protein with 56 additional residues. Quantitative RT-PCR detected both FAM161A variants in all tissues examined. The short variant showed highest expression in testis, followed by retina, heart, and liver. The long variant showed highest expression in retina, followed by testis, liver, heart, and muscle. Expression in mouse retina was developmentally regulated, with minimal expression in the neural basal layer at postnatal day 0 and expression in all cell bodies of the outer nuclear layer at postnatal day 10. In adult retina, Fam161a was present in the inner segments, but not the outer segments, of photoreceptors, and it was expressed in outer plexiform layer.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Family With Sequence Similarity 161, Member A (FAM161A) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Family With Sequence Similarity 161, Member A (FAM161A) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Family With Sequence Similarity 161, Member A (FAM161A) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Family With Sequence Similarity 161, Member A (FAM161A) CLIA Kit Customized Service Offer
n/a ELISA Kit for Family With Sequence Similarity 161, Member A (FAM161A) ELISA Kit Customized Service Offer

Organism species: Mus musculus (Mouse)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Family With Sequence Similarity 161, Member A (FAM161A) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Family With Sequence Similarity 161, Member A (FAM161A) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Family With Sequence Similarity 161, Member A (FAM161A) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Family With Sequence Similarity 161, Member A (FAM161A) CLIA Kit Customized Service Offer
n/a ELISA Kit for Family With Sequence Similarity 161, Member A (FAM161A) ELISA Kit Customized Service Offer

Organism species: Rattus norvegicus (Rat)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Family With Sequence Similarity 161, Member A (FAM161A) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Family With Sequence Similarity 161, Member A (FAM161A) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Family With Sequence Similarity 161, Member A (FAM161A) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Family With Sequence Similarity 161, Member A (FAM161A) CLIA Kit Customized Service Offer
n/a ELISA Kit for Family With Sequence Similarity 161, Member A (FAM161A) ELISA Kit Customized Service Offer
  1. "The full-ORF clone resource of the German cDNA consortium."BMC Genomics 8:399-399(2007) [PubMed] [Europe PMC] [Abstract]
  2. "Generation and annotation of the DNA sequences of human chromosomes 2 and 4." Nature 434:724-731(2005) [PubMed] [Europe PMC] [Abstract]
  3. "Complete sequencing and characterization of 21,243 full-length human cDNAs." Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract]
  4. "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
  5. "Nonsense mutations in FAM161A cause RP28-associated recessive retinitis pigmentosa."Am. J. Hum. Genet. 87:376-381(2010) [PubMed] [Europe PMC] [Abstract]
  6. "Homozygosity mapping reveals null mutations in FAM161A as a cause of autosomal-recessive retinitis pigmentosa."Am. J. Hum. Genet. 87:382-391(2010) [PubMed] [Europe PMC] [Abstract]
  7. "FAM161A, associated with retinitis pigmentosa, is a component of the cilia-basal body complex and interacts with proteins involved in ciliopathies."Hum. Mol. Genet. 21:5174-5184(2012) [PubMed] [Europe PMC] [Abstract]
  8. "The retinitis pigmentosa 28 protein FAM161A is a novel ciliary protein involved in intermolecular protein interaction and microtubule association."Hum. Mol. Genet. 21:4573-4586(2012) [PubMed] [Europe PMC] [Abstract]
  9. "Disruption of the basal body protein POC1B results in autosomal-recessive cone-rod dystrophy." Am. J. Hum. Genet. 95:131-142(2014) [PubMed] [Europe PMC] [Abstract]