F8 S392L [extracellular region]

Stable Identifier
R-HSA-9667123
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
FVIII S392L
F8 S392L [extracellular region] icon
Locations in the PathwayBrowser
Literature References
PubMed ID Title Journal Year
8052958 Factor VIII S373L: mutation at P1' site confers thrombin cleavage resistance, causing mild haemophilia A

O'Brien, DP, Tuddenham, EG, Pemberton, S, Acquila, M, Mori, PG, Johnson, DJ

Thromb. Haemost. 1994
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-serine 392 replaced with L-leucine
Coordinate
392
PsiMod
A protein modification that effectively removes or replaces an L-serine.
A protein modification that effectively converts a source amino acid residue to an L-leucine.
Disease
Name Identifier Synonyms
factor VIII deficiency DOID:12134 Congenital factor VIII disorder, Subhemophilia, Hemophilia A
Cross References
ClinGen
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