Reticulocalbin 2

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

Reticulocalbin-2 is a protein that in humans is encoded by the RCN2 gene.[5][6][7]

AliasesRCN2, E6BP, ERC-55, ERC55, TCBP49, reticulocalbin 2
End76,954,393 bp[1]
Quick facts RCN2, Identifiers ...
RCN2
Identifiers
AliasesRCN2, E6BP, ERC-55, ERC55, TCBP49, reticulocalbin 2
External IDsOMIM: 602584; MGI: 1349765; HomoloGene: 2176; GeneCards: RCN2; OMA:RCN2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_002902
NM_001271837

NM_001278274
NM_011992

RefSeq (protein)

NP_001258766
NP_002893

NP_001265203
NP_036122

Location (UCSC)Chr 15: 76.93 – 76.95 MbChr 9: 55.95 – 55.97 Mb
PubMed search[3][4]
Wikidata
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Reticulocalbin 2 is a calcium-binding protein located in the lumen of the ER. The protein contains six conserved regions with similarity to a high affinity Ca(+2)-binding motif, the EF-hand. The RCN2 gene maps to the same region as type 4 Bardet-Biedl syndrome (MIM:600374), suggesting a possible causative role for reticulocalbin 2 in the disorder.[7]

References

Further reading

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