MCFD2

MCFD2
Identifiers
Aliases	MCFD2, F5F8D, F5F8D2, LMAN1IP, SDNSF, multiple coagulation factor deficiency 2, multiple coagulation factor deficiency 2, ER cargo receptor complex subunit
External IDs	OMIM: 607788; MGI: 2183439; HomoloGene: 44552; GeneCards: MCFD2; OMA:MCFD2 - orthologs
Available structures
PDB	Ortholog search: PDBe RCSB
List of PDB id codes
	2VRG, 3A4U, 3LCP, 3WHT, 3WHU, 3WNX, 4YGE, 4YGD, 4YGB, 4YGC
Gene location (Human)
Chr.	Chromosome 2 (human)
End	46,941,855 bp
Gene location (Mouse)
Chr.	Chromosome 17 (mouse)
End	87,573,363 bp
RNA expression pattern
	Top expressed in
	parotid gland; ; seminal vesicula; ; pericardium; ; stromal cell of endometrium; ; left adrenal gland; ; adrenal cortex; ; right adrenal gland; ; right adrenal cortex; ; left adrenal cortex; ; body of pancreas;
	Top expressed in
	parotid gland; ; lacrimal gland; ; decidua; ; seminal vesicula; ; stroma of bone marrow; ; submandibular gland; ; gastrula; ; left lobe of liver; ; pyloric antrum; ; right kidney;
	More reference expression data
	; ;
	More reference expression data
Gene ontology
Molecular function	calcium ion binding; metal ion binding; protein binding;
Cellular component	ER to Golgi transport vesicle membrane; Golgi apparatus; endoplasmic reticulum membrane; endoplasmic reticulum; endoplasmic reticulum-Golgi intermediate compartment membrane; endoplasmic reticulum-Golgi intermediate compartment; Golgi membrane;
Biological process	protein transport; endoplasmic reticulum to Golgi vesicle-mediated transport; COPII vesicle coating; vesicle-mediated transport; protein N-linked glycosylation via asparagine;
	Sources:Amigo / QuickGO
Orthologs
	90411
	193813
	ENSG00000180398
	ENSMUSG00000024150
	Q8NI22
	Q8K5B2
NM_139279; NM_001171506; NM_001171507; NM_001171508; NM_001171509;
	NM_001171510; NM_001171511
	NM_139295; NM_176808
NP_001164977; NP_001164978; NP_001164979; NP_001164980; NP_001164981;
	NP_001164982; NP_644808
	NP_647456; NP_789778
	Wikidata
View/Edit Human	View/Edit Mouse

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.

References

1 2 3 GRCh38: Ensembl release 89: ENSG00000180398 – Ensembl, May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000024150 – Ensembl, May 2017
↑ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
↑ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
↑ Zhang B, Cunningham MA, Nichols WC, Bernat JA, Seligsohn U, Pipe SW, McVey JH, Schulte-Overberg U, de Bosch NB, Ruiz-Saez A, White GC, Tuddenham EG, Kaufman RJ, Ginsburg D (May 2003). "Bleeding due to disruption of a cargo-specific ER-to-Golgi transport complex". Nat Genet. 34 (2): 220–5. doi:10.1038/ng1153. PMID 12717434. S2CID 19281158.
↑ Deka N, Wong E, Matera AG, Kraft R, Leinwand LA, Schmid CW (Mar 1989). "Repetitive nucleotide sequence insertions into a novel calmodulin-related gene and its processed pseudogene". Gene. 71 (1): 123–34. doi:10.1016/0378-1119(88)90084-4. PMID 2463956.
↑ "Entrez Gene: MCFD2 multiple coagulation factor deficiency 2".

Nyfeler B, Zhang B, Ginsburg D, et al. (2007). "Cargo selectivity of the ERGIC-53/MCFD2 transport receptor complex" (PDF). Traffic. 7 (11): 1473–81. doi:10.1111/j.1600-0854.2006.00483.x. PMID 17010120. S2CID 22483569.
Mohanty D, Ghosh K, Shetty S, et al. (2005). "Mutations in the MCFD2 gene and a novel mutation in the LMAN1 gene in Indian families with combined deficiency of factor V and VIII". Am. J. Hematol. 79 (4): 262–6. doi:10.1002/ajh.20397. PMID 16044454. S2CID 30602878.
Zhang B, Kaufman RJ, Ginsburg D (2005). "LMAN1 and MCFD2 form a cargo receptor complex and interact with coagulation factor VIII in the early secretory pathway". J. Biol. Chem. 280 (27): 25881–6. doi:10.1074/jbc.M502160200. PMID 15886209.
Hillier LW, Graves TA, Fulton RS, et al. (2005). "Generation and annotation of the DNA sequences of human chromosomes 2 and 4". Nature. 434 (7034): 724–31. Bibcode:2005Natur.434..724H. doi:10.1038/nature03466. PMID 15815621.
Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
Spatuzza C, Renna M, Faraonio R, et al. (2004). "Heat shock induces preferential translation of ERGIC-53 and affects its recycling pathway". J. Biol. Chem. 279 (41): 42535–44. doi:10.1074/jbc.M401860200. PMID 15292203.
Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
Toda H, Tsuji M, Nakano I, et al. (2003). "Stem cell-derived neural stem/progenitor cell supporting factor is an autocrine/paracrine survival factor for adult neural stem/progenitor cells". J. Biol. Chem. 278 (37): 35491–500. doi:10.1074/jbc.M305342200. PMID 12832409.
Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
Nichols WC, Terry VH, Wheatley MA, et al. (1999). "ERGIC-53 gene structure and mutation analysis in 19 combined factors V and VIII deficiency families". Blood. 93 (7): 2261–6. PMID 10090935.
Neerman-Arbez M, Johnson KM, Morris MA, et al. (1999). "Molecular analysis of the ERGIC-53 gene in 35 families with combined factor V-factor VIII deficiency". Blood. 93 (7): 2253–60. doi:10.1182/blood.V93.7.2253. PMID 10090934.

This article on a gene on human chromosome 2 is a stub. You can help Wikipedia by adding missing information.

[refGRCh38Ensembl-1] 1 2 3 GRCh38: Ensembl release 89: ENSG00000180398 – Ensembl, May 2017

[refGRCm38Ensembl-2] 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000024150 – Ensembl, May 2017

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[pmid12717434-5] Zhang B, Cunningham MA, Nichols WC, Bernat JA, Seligsohn U, Pipe SW, McVey JH, Schulte-Overberg U, de Bosch NB, Ruiz-Saez A, White GC, Tuddenham EG, Kaufman RJ, Ginsburg D (May 2003). "Bleeding due to disruption of a cargo-specific ER-to-Golgi transport complex". Nat Genet. 34 (2): 220–5. doi:10.1038/ng1153. PMID 12717434. S2CID 19281158.

[pmid2463956-6] Deka N, Wong E, Matera AG, Kraft R, Leinwand LA, Schmid CW (Mar 1989). "Repetitive nucleotide sequence insertions into a novel calmodulin-related gene and its processed pseudogene". Gene. 71 (1): 123–34. doi:10.1016/0378-1119(88)90084-4. PMID 2463956.

[entrez-7] "Entrez Gene: MCFD2 multiple coagulation factor deficiency 2".

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References

Further reading