PABPN1 Chromosome 14

Poly(A) binding protein nuclear 1
10 variants 10 Health Risk

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What This Gene Does
This gene encodes an abundant nuclear protein that binds with high affinity to nascent poly(A) tails. The protein is required for progressive and efficient polymerization of poly(A) tails at the 3' ends of eukaryotic transcripts and controls the size of the poly(A) tail to about 250 nt. At steady-state, this protein is localized in the nucleus whereas a different poly(A) binding protein is localized in the cytoplasm. This gene contains a GCG trinucleotide repeat at the 5' end of the coding region, and expansion of this repeat from the normal 6 copies to 8-13 copies leads to autosomal dominant oculopharyngeal muscular dystrophy (OPMD) disease. Related pseudogenes have been identified on chromosomes 19 and X. Read-through transcription also exists between this gene and the neighboring upstream BCL2-like 2 (BCL2L2) gene. [provided by RefSeq, Dec 2010]
Gene Info
Gene Group
RNA binding motif containing
Locus Type
gene with protein product
Location
14q11.2
Ensembl
ENSG00000100836
Associated Conditions (4)
Oculopharyngeal muscular dystrophy 1
PABPN1-related disorder
Oculopharyngeal muscular dystrophy
Inborn genetic diseases
Key Variants
All Variants (10)
RSID Category Clinical Significance Conditions
RS1045060319 Health Risk Conflicting classifications of pathogenicity Oculopharyngeal muscular dystrophy 1, Oculopharyngeal muscular dystrophy 1
RS1401656265 Health Risk Conflicting classifications of pathogenicity Oculopharyngeal muscular dystrophy 1, Oculopharyngeal muscular dystrophy 1
RS1433496791 Health Risk Conflicting classifications of pathogenicity Oculopharyngeal muscular dystrophy 1, Oculopharyngeal muscular dystrophy 1
RS947151586 Health Risk Conflicting classifications of pathogenicity PABPN1-related disorder, Oculopharyngeal muscular dystrophy 1, PABPN1-related disorder
RS1337792814 Health Risk Pathogenic Oculopharyngeal muscular dystrophy 1, Oculopharyngeal muscular dystrophy 1
RS1888253108 Health Risk Pathogenic
RS1888255467 Health Risk Pathogenic
RS193922941 Health Risk Pathogenic Oculopharyngeal muscular dystrophy 1, Oculopharyngeal muscular dystrophy, Inborn genetic diseases
RS1594987281 Health Risk Pathogenic/Likely pathogenic Oculopharyngeal muscular dystrophy, Oculopharyngeal muscular dystrophy
RS1888252890 Health Risk Pathogenic/Likely pathogenic Oculopharyngeal muscular dystrophy 1, Oculopharyngeal muscular dystrophy 1
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