PRKD3 protein kinase D3
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 58 |
Ranking
ClinVar | |
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0 |
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0 |
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2 |
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60 |
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0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
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Target data | : |
MGeND data only
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
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Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | EPK2 |
SYNONYM | PKC-NU |
SYNONYM | PKD3 |
SYNONYM | PRKCN |
SYNONYM | nPKC-NU |
MIM | 607077 OMIM |
HGNC | HGNC:9408 HGNC |
Ensembl | ENSG00000115825 Ensembl |
AllianceGenome | HGNC:9408 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000379066.5 | hg38 | chr2 | 37,250,502 | 37,317,894 | 67,393 |
ENST00000234179.8 | hg38 | chr2 | 37,250,502 | 37,324,833 | 74,332 |
ENST00000379066.5 | hg19 | chr2 | 37,477,645 | 37,545,037 | 67,393 |
ENST00000234179.8 | hg19 | chr2 | 37,477,645 | 37,551,976 | 74,332 |
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