MAPKAPK5 MAPK activated protein kinase 5
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 10 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 34 |
Ranking
ClinVar | |
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0 |
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0 |
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2 |
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36 |
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8 |
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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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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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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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 | MAPKAP-K5 |
SYNONYM | MK-5 |
SYNONYM | MK5 |
SYNONYM | NCFD |
SYNONYM | PRAK |
MIM | 606723 OMIM |
HGNC | HGNC:6889 HGNC |
Ensembl | ENSG00000089022 Ensembl |
AllianceGenome | HGNC:6889 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000550735.7 | hg38 | chr12 | 111,842,228 | 111,902,222 | 59,995 |
ENST00000551404.7 | hg38 | chr12 | 111,842,013 | 111,893,161 | 51,149 |
ENST00000547305.1 | hg38 | chr12 | 111,842,475 | 111,843,396 | 922 |
ENST00000551404.7 | hg19 | chr12 | 112,279,817 | 112,330,965 | 51,149 |
ENST00000550735.7 | hg19 | chr12 | 112,280,032 | 112,340,026 | 59,995 |
ENST00000547305.1 | hg19 | chr12 | 112,280,279 | 112,281,200 | 922 |
Key | Value |
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strand | + |
UniProt | TSG |
start | 112,280,031 |
Gene Symbol | MAPKAPK5 |
Entrez GeneId | 8,550 |
Chr Band | 12q24.13 |
end | 112,331,227 |
chr | chr12 |
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