MCFD2

Protein-coding gene in humans From Wikipedia, the free encyclopedia

Multiple coagulation factor deficiency protein 2 is a protein that in humans is encoded by the MCFD2 gene.[5][6][7] Mutations in MCFD2 cause the combined deficiency of factor V and factor VIII (F5F8D), a recessive bleeding disorder. MCFD2 and ERGIC-53 (or LMAN1) form a protein complex and serve as a cargo receptor to transport FV and FVIII from the ER to the Golgi body. Mutations in LMAN1 gene (encoding ERGIC-53 or LMAN1) also cause F5F8D.

PDBOrtholog search: PDBe RCSB
AliasesMCFD2, F5F8D, F5F8D2, LMAN1IP, SDNSF, multiple coagulation factor deficiency 2, multiple coagulation factor deficiency 2, ER cargo receptor complex subunit
Quick facts Available structures, PDB ...
MCFD2
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesMCFD2, F5F8D, F5F8D2, LMAN1IP, SDNSF, multiple coagulation factor deficiency 2, multiple coagulation factor deficiency 2, ER cargo receptor complex subunit
External IDsOMIM: 607788; MGI: 2183439; HomoloGene: 44552; GeneCards: MCFD2; OMA:MCFD2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_139295
NM_176808

RefSeq (protein)

NP_647456
NP_789778

Location (UCSC)Chr 2: 46.9 – 46.94 MbChr 17: 87.56 – 87.57 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse
Close

References

Further reading

Related Articles

Wikiwand AI