PD mutation database
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Table of contents
Detail information
Sequence information
Mutation Search
Mutation & Clinical information
Multiple alignments
3D structure
Structure information
Overview of mutations
Reference information
Causative genes
PARK7
LRRK2
GBA
HTRA2
NR4A2
PARK2
PINK1
SNCA
SNCG
UCHL1
SNCAIP
Related genes
GPR37
MTX1
SNCB
Link
PubMed
OMIM
Ensembl
PDB
JSNP
World Parkinson Disease Association
PINK1PTEN induced putative kinase 1
Detail information
Gene Symbol
PINK1
Full name
PTEN induced putative kinase 1
Synonym
BRPK, FLJ27236, PARK6
Genome position
chromosome: 1; Location: 1p36
20959947 .. 20978003 (strand : +)
Links
EntrezGene
UCSC
OMIM
The GRCh37/hg19 sequence assembly is used for the human genomic reference sequence.
Sequence information
Exon : Intron
100:1
50:1
10:1
3:1
1:1
Age onset & duration
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expanded image
a.a. :
Q9BXM7
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mRNA :
AB053323.1
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Mutation Search
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Mutation & Clinical information
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Experimental Data only
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Multiple alignments
Multiple alignments of all patients' sequences
(Registration is needed to see this information, because unpublished data is contained.)
Multiple alignments of orthologous sequences
3D structure
3D Structure data is not found.
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Structure information
Exon
Start AA
End AA
Structure
1
1
77
Transit peptide
1, 2, 3, 4, 5, 6, 7, 8
78
581
Chain
1, 2, 3, 4, 5, 6, 7
156
511
Domain
2
162
170
Nucleotide phosphate-binding region
5
362
362
Active site
2
186
186
Binding site
1, 2, 3, 4
1
307
Splice variant
4
308
320
Splice variant
4
305
305
Sequence variant
4
309
309
Sequence variant
4
340
340
Sequence variant
7
521
521
Sequence variant
2
209
209
Sequence conflict
6
419
419
Sequence conflict
Overview of mutations
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(Registration is needed to see this information, because unpublished data is contained.)
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