Peflin

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Peflin is a protein that in humans is encoded by the PEF1 gene.[5][6][7]

AliasesPEF1, ABP32, PEF1A, penta-EF-hand domain containing 1
End31,644,896 bp[1]
Quick facts PEF1, Identifiers ...
PEF1
Identifiers
AliasesPEF1, ABP32, PEF1A, penta-EF-hand domain containing 1
External IDsOMIM: 610033; MGI: 1915148; HomoloGene: 56569; GeneCards: PEF1; OMA:PEF1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_012392
NM_001359651

NM_026441

RefSeq (protein)

NP_036524
NP_001346580

NP_080717

Location (UCSC)Chr 1: 31.63 – 31.64 MbChr 4: 130 – 130.02 Mb
PubMed search[3][4]
Wikidata
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PEF1 is a Ca(2+)-binding protein that belongs to the penta-EF hand (PEF) protein family, which includes the calpain small subunit (CAPNS1; MIM 114170), sorcin (SRI; MIM 182520), grancalcin (GCA; MIM 607030), and ALG2 (PDCD6; MIM 601057) (Kitaura et al., 2001).[supplied by OMIM][7]

Interactions

PEF1 has been shown to interact with PDCD6.[8]

References

Further reading

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