PRDM13 cDNA ORF clone, Homo sapiens(human)

North Carolina macular dystrophy (MCDR1) caused by a novel tandem duplication of the
Bowne SJ, Sullivan LS, Wheaton DK, Locke KG, Jones KD, Koboldt DC, Fulton RS, Wilson RK, Blanton SH, Birch DG, Daiger SP
Molecular vision221239-1247(2016)

Deficiency of Prdm13, a dorsomedial hypothalamus-enriched gene, mimics age-associated changes in sleep quality and adiposity.
Satoh A, Brace CS, Rensing N, Imai S
Aging cell14(2)209-18(2015 Apr)

Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.
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The DNA sequence and analysis of human chromosome 6.
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Nature425(6960)805-11(2003 Oct)

The duplication found in the RFS355 family is distinct from the previously reported duplication and provides additional support that dysregulation of PRDM13, not CCNC, is the cause of NCMD mapped to the MCDR1 locus.
Title: North Carolina macular dystrophy (MCDR1) caused by a novel tandem duplication of the

Findings indicate that Prdm13/Nkx2-1-mediated signaling in the DMC declines with advanced age, leading to decreased sleep quality and increased adiposity.
Title: Deficiency of Prdm13, a dorsomedial hypothalamus-enriched gene, mimics age-associated changes in sleep quality and adiposity.