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MCFD2

multiple coagulation factor deficiency 2, ER cargo receptor complex subunit

HCNC Approved Symbol
MCFD2 (HGNC:18451)
Genomic Coordinates
2:46,901,870 - 46,941,855 (2p21)
Synonyms
F5F8D, LMAN1IP, SDNSF
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the MCFD2 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results
MCFD2 - Gene browser | 3billion