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Gene information for MCFD2 (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID90411
Official gene symbolMCFD2
Full namemultiple coagulation factor deficiency 2
Aliases,DKFZp686G21263,F5F8D,LMAN1IP,SDNSF,
Gene summaryThis gene encodes a soluble luminal protein with two calmodulin-like EF-hand motifs at its C-terminus. This protein forms a complex with LAMN1 (lectin mannose binding protein 1; also known as ERGIC-53) that facilitates the transport of coagulation factors V (FV) and VIII (FVIII) from the endoplasmic reticulum to the Golgi apparatus via an endoplasmic reticulum Golgi intermediate compartment (ERGIC). Mutations in this gene cause combined deficiency of FV and FVIII (F5F8D); a rare autosomal recessive bleeding disorder characterized by mild to moderate bleeding and coordinate reduction in plasma FV and FVIII levels. This protein has also been shown to maintain stem cell potential in adult central nervous system and is a marker for testicular germ cell tumors. The 3' UTR of this gene contains a transposon-like human repeat element named 'THE 1'. A processed RNA pseudogene of this gene is on chromosome 6p22.1. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq]
LocationChromosome: 2   Locus: 2p21
Gene position47168994 - 47129009  Map Viewer
Gene orientationminus
Gene size39986 bp
Gene sequence
OMIM ID607788