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Mutations on the Protein: P08100 From Positions: 87 To 104

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5
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4





Swiss-Prot Disease: VAR_004782
p.GLY89ASP
N/A
N/A
Retinitis pigmentosa 4 (RP4)


Swiss-Prot Disease: VAR_004783
p.GLY90ASP
N/A
N/A
Night blindness, congenital stationary, autosomal dominant 1 (CSNBAD1)


Swiss-Prot Disease: VAR_004784
p.THR94ILE
N/A
N/A
Night blindness, congenital stationary, autosomal dominant 1 (CSNBAD1)


Swiss-Prot Disease: VAR_004781
p.VAL87ASP
N/A
N/A
Retinitis pigmentosa 4 (RP4)


Swiss-Prot Polymorphism: VAR_004785
p.VAL104ILE
N/A
N/A
N/A


OMIM Disease: 180380.0009
p.GLY89ASP
N/A
N/A
RETINITIS PIGMENTOSA 4


OMIM Disease: 180380.0032
p.GLY90ASP
N/A
N/A
NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 1


OMIM Disease: 180380.0042
p.THR94ILE
N/A
N/A
NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 1


OMIM Disease: 180380.0008
p.VAL87ASP
N/A
N/A
RETINITIS PIGMENTOSA 4






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