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A1CF

A1CF
Protein ACF PDB 2cpd.png
Available structures
PDB Ortholog search: PDBe RCSB
Identifiers
Aliases A1CF, ACF, ACF64, ACF65, APOBEC1CF, ASP, APOBEC1 complementation factor
External IDs MGI: 1917115 HomoloGene: 16363 GeneCards: A1CF
Gene location (Human)
Chromosome 10 (human)
Chr. Chromosome 10 (human)
Chromosome 10 (human)
Genomic location for A1CF
Genomic location for A1CF
Band 10q11.23 Start 50,799,409 bp
End 50,885,675 bp
RNA expression pattern
PBB GE ACF 220951 s at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001081074

RefSeq (protein)

NP_001074543

Location (UCSC) Chr 10: 50.8 – 50.89 Mb Chr 10: 31.87 – 31.95 Mb
PubMed search

2CPD

NM_138933

NM_001081074

NP_620311

NP_001074543

APOBEC1 complementation factor is a protein that in humans is encoded by the A1CF gene.

Alternative splicing occurs at this locus and three full-length transcript variants, encoding three distinct isoforms, have been described. Additional splicing has been observed but the full-length nature of these variants has not been determined.

Mammalian apolipoprotein B mRNA undergoes site-specific C to U deamination, which is mediated by a multi-component enzyme complex containing a minimal core composed of APOBEC1 and a complementation factor encoded by this gene. The gene product has three non-identical RNA recognition motifs and belongs to the hnRNP R family of RNA-binding proteins. It has been proposed that this complementation factor functions as an RNA-binding subunit and docks APOBEC1 to deaminate the upstream cytidine. Studies suggest that the protein may also be involved in other RNA editing or RNA processing events.


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