Antigen Record Ag003444

AgACCAg003444
Date19-08-2008
Last updated14-12-2016
Antigen NameTYR
Common NameTyrosinase
Full NameTyrosinase
SynonymMonophenol monooxygenase; Tumor rejection antigen AB; Tyrosinase precursor; tyrosinase (oculocutaneous albinism IA); TYR; EC 1.14.18.1; LB24-AB; OCA1A; OCAIA; SK29-AB

another display format
  • Monophenol monooxygenase
  • Tumor rejection antigen AB
  • Tyrosinase precursor
  • tyrosinase (oculocutaneous albinism IA)
  • TYR
  • EC 1.14.18.1
  • LB24-AB
  • OCA1A
  • OCAIA
  • SK29-AB
UniProt IDP14679
NCBI Gene ID7299
GeneCard IDGC11P089177
SwissProt VARIANT IDVAR_021714
CommentOculocutaneous albinism type IA (OCA-IA) - Defects in TYR are the cause of oculocutaneous albinism type IA. OCA-I, also known as tyrosinase negative oculocutaneous albinism, is an autosomal recessive disorder characterized by absence of pigment in hair, skin and eyes. OCA-I is divided into 2 types
AnnotationThis is a fragment sequence.
IsoformsAg000039,  Ag000040

Alignment of all Isoforms
Mutation entriesAg000190,  Ag000192,  Ag000193,  Ag003362,  Ag003363,  Ag003364,  Ag003365,  Ag003366,  Ag003367,  Ag003368,  Ag003369,  Ag003370,  Ag003371,  Ag003372,  Ag003373,  Ag003374
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View mutation map
RNA/protein expression profileRNA and protein Expression profile
T cell epitopeEpitope sequencePositionHLA alleleReference
LHHAFVDSIF11-20 B38  16247014
Predicted HLA binders
Allele:  predictions
Peptide length:   
Reference sequenceQGSANDPIFLLHHAFVDSIFEQWLRRHRPLQEVYPEANAPI
Antigen sequenceQGSANDPIFLLHHAFVDSIFVQWLRRHRPLQEVYPEANAPI