F8(392-759) I585T [plasma membrane]

Stable Identifier
R-HSA-9668357
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
Synonyms
FVIIIa I585T A2 polypeptide
F8(392-759) I585T  [plasma membrane] icon
Locations in the PathwayBrowser
Literature References
PubMed ID Title Journal Year
9427707 The molecular basis for cross-reacting material-positive hemophilia A due to missense mutations within the A2-domain of factor VIII

Amano, K, Kaufman, RJ, Kazazian, HH, Pemberton, S, Kemball-Cook, G, Sarkar, R

Blood 1998
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-isoleucine 585 replaced with L-threonine
Coordinate
585
PsiMod
A protein modification that effectively removes or replaces an L-isoleucine.
A protein modification that effectively converts a source amino acid residue to L-threonine.
Disease
Name Identifier Synonyms
factor VIII deficiency DOID:12134 Congenital factor VIII disorder, Subhemophilia, Hemophilia A
Cross References
Guide to Pharmacology - Targets
ClinGen
OpenTargets
ZINC - Substances
ZINC target
PRO
GlyGen
GeneCards
F8
Pharos - Targets
Orphanet
F8
ZINC - Predictions - Purchasable
HMDB Protein
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