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Mutations on the Protein: P04156 From Positions: 177 To 190

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Swiss-Prot Disease: VAR_006469
p.ASP178ASN
N/A
N/A
Fatal familial insomnia (FFI)


Swiss-Prot Disease: VAR_008746
p.HIS187ARG
N/A
N/A
Gerstmann-Straussler disease (GSD)


Swiss-Prot Polymorphism: VAR_006471
p.THR183ALA
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_008747
p.THR188ARG
N/A
N/A
N/A


Swiss-Prot Polymorphism: VAR_008748
p.THR188LYS
N/A
N/A
N/A


Swiss-Prot Disease: VAR_006470
p.VAL180ILE
N/A
N/A
Creutzfeldt-Jakob disease (CJD)


OMIM Disease: 176640.0007,176640.0010
p.ASP178ASN
N/A
N/A
FATAL FAMILIAL INSOMNIA||CREUTZFELDT-JAKOB DISEASE, INCLUDED


OMIM Disease: 176640.0024
p.HIS187ARG
N/A
N/A
GERSTMANN-STRAUSSLER DISEASE||SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES, INCLUDED


OMIM Disease: 176640.0022
p.THR183ALA
N/A
N/A
SPONGIFORM ENCEPHALOPATHY WITH NEUROPSYCHIATRIC FEATURES


OMIM Disease: 176640.0016
p.VAL180ILE
N/A
N/A
CREUTZFELDT-JAKOB DISEASE






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