F8 Y1699F [extracellular region]

Stable Identifier
R-HSA-9665829
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
FVIII light chain Y1699F
F8 Y1699F [extracellular region] icon
Locations in the PathwayBrowser
Literature References
PubMed ID Title Journal Year
21909383 Storage of factor VIII variants with impaired von Willebrand factor binding in Weibel-Palade bodies in endothelial cells

van den Biggelaar, M, Bouwens, EA, Voorberg, J, Mertens, K

PLoS ONE 2011
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-tyrosine 1699 replaced with L-phenylalanine
Coordinate
1699
PsiMod
A protein modification that effectively converts a source amino acid residue to L-phenylalanine.
A protein modification that effectively removes or replaces an L-tyrosine.
Disease
Name Identifier Synonyms
factor VIII deficiency DOID:12134 Congenital factor VIII disorder, Subhemophilia, Hemophilia A
Cross References
ClinGen
Mondo
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