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MMM1013-7512149 Probe Detail
Nucleotide
Probe/Clone
  • Name
    MMM1013-7512149
  • Sequence Type
    cDNA
  • ID
    MGI:4942175
  • Region Covered
    corresponding to the splice variant lacking exon 4
  • Vector Type
    Plasmid
Source
  • Species
    mouse, laboratory
  • Tissue
    retina
Genes
Fam161a family with sequence similarity 161, member A
Expression
  • Assay Results
    9
References
J:169188 Bandah-Rozenfeld D, et al., Homozygosity mapping reveals null mutations in FAM161A as a cause of autosomal-recessive retinitis pigmentosa. Am J Hum Genet. 2010 Sep 10;87(3):382-91
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Funding Information
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Send questions and comments to User Support. 		last database update
05/14/2024
MGI 6.23 		The Jackson Laboratory