PKN2 protein kinase N2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
not provided | 1 | 0 |
Uncertain significance | 0 | 64 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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66 |
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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
Locus Zoom
Variants
Search Word
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 | PAK2 |
SYNONYM | PRK2 |
SYNONYM | PRKCL2 |
SYNONYM | PRO2042 |
SYNONYM | Pak-2 |
SYNONYM | STK7 |
MIM | 602549 OMIM |
HGNC | HGNC:9406 HGNC |
Ensembl | ENSG00000065243 Ensembl |
AllianceGenome | HGNC:9406 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000316005.11 | hg38 | chr1 | 88,684,222 | 88,806,268 | 122,047 |
ENST00000370521.8 | hg38 | chr1 | 88,684,273 | 88,836,255 | 151,983 |
ENST00000370513.9 | hg38 | chr1 | 88,684,573 | 88,833,519 | 148,947 |
ENST00000316005.11 | hg19 | chr1 | 89,149,905 | 89,271,951 | 122,047 |
ENST00000370521.8 | hg19 | chr1 | 89,149,956 | 89,301,938 | 151,983 |
ENST00000370513.9 | hg19 | chr1 | 89,150,256 | 89,299,202 | 148,947 |
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