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Mutations on the Protein: Q9NZW4 From Positions: 0 To 65

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7
0
4



Swiss-Prot Disease: VAR_036862
p.ALA15VAL
N/A
N/A
Dentinogenesis imperfecta, Shields type 2 (DGI2)


Swiss-Prot Disease: VAR_070252
p.PRO17LEU
N/A
N/A
Dentinogenesis imperfecta, Shields type 3 (DGI3)


Swiss-Prot Polymorphism: VAR_054443
p.PRO17SER
N/A
N/A
N/A


Swiss-Prot Disease: VAR_012280
p.PRO17THR
N/A
N/A
Deafness, autosomal dominant, 39, with dentinogenesis imperfecta 1 (DFNA39/DGI1)


Swiss-Prot Disease: VAR_036861
p.TYR6ASP
N/A
N/A
Dentin dysplasia 2 (DTDP2)


Swiss-Prot Disease: VAR_070253
p.VAL18ASP
N/A
N/A
Dentinogenesis imperfecta, Shields type 2 (DGI2)


Swiss-Prot Disease: VAR_012281
p.VAL18PHE
N/A
N/A
Dentinogenesis imperfecta, Shields type 3 (DGI3)


OMIM Disease: 125485.0007
p.ALA15VAL
N/A
N/A
DENTINOGENESIS IMPERFECTA, SHIELDS TYPE II


OMIM Disease: 125485.0005
p.ASP6TYR
N/A
N/A
DENTIN DYSPLASIA, TYPE II


OMIM Disease: 125485.0001
p.GLN45TER
N/A
N/A
DENTINOGENESIS IMPERFECTA, SHIELDS TYPE II


OMIM Disease: 125485.0003
p.PRO17THR
N/A
N/A
DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL 39, WITH DENTINOGENESIS||IMPERFECTA 1






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