F8 R2016W [endoplasmic reticulum lumen]

Stable Identifier
R-HSA-9666355
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
FVIII R2016W
F8 R2016W [endoplasmic reticulum lumen] icon
Locations in the PathwayBrowser
Literature References
PubMed ID Title Journal Year
29170251 Clustered F8 missense mutations cause hemophilia A by combined alteration of splicing and protein biosynthesis and activity

Peyvandi, F, Garagiola, I, McVey, JH, Pinotti, M, Branchini, A, Donadon, I, Bernardi, F, Mortarino, M

Haematologica 2018
External Reference Information
External Reference
Gene Names
F8, F8C
Chain
signal peptide:1-19, chain:20-2351, chain:20-1332, chain:20-759, chain:760-1332, chain:1668-2351
Participates
Other forms of this molecule
Modified Residues
Name
L-arginine 2016 replaced with L-tryptophan
Coordinate
2016
PsiMod
A protein modification that effectively converts a source amino acid residue to L-tryptophan.
A protein modification that effectively removes or replaces an L-arginine.
Disease
Name Identifier Synonyms
factor VIII deficiency DOID:12134 Congenital factor VIII disorder, Subhemophilia, Hemophilia A
Cross References
ClinGen
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