MAP2K6 mitogen-activated protein kinase kinase 6
Information
- Symbol
- MAP2K6
- Type
- protein-coding
- Description
- mitogen-activated protein kinase kinase 6
- Entrez Gene ID
- 5608
- Genome
- hg19
- Position
- chr17:67,410,838-67,550,006
- Genome
- hg38
- Position
- chr17:69,414,697-69,553,865
- MIM
- 601254 OMIM
- HGNC
- HGNC:6846 HGNC
- Ensembl
- ENSG00000108984 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 14 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
14 |
 |
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
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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| Filtering | : |
| Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | MAPKK6 |
| SYNONYM | MEK6 |
| SYNONYM | MKK6 |
| SYNONYM | PRKMK6 |
| SYNONYM | SAPKK-3 |
| SYNONYM | SAPKK3 |
| MIM | 601254 OMIM |
| HGNC | HGNC:6846 HGNC |
| Ensembl | ENSG00000108984 Ensembl |
| AllianceGenome | HGNC:6846 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000590474.7 | hg38 | chr17 | 69,414,697 | 69,553,865 | 139,169 |
| ENST00000589647.5 | hg38 | chr17 | 69,502,429 | 69,542,019 | 39,591 |
| ENST00000590474.7 | hg19 | chr17 | 67,410,838 | 67,550,006 | 139,169 |
| ENST00000589647.5 | hg19 | chr17 | 67,498,570 | 67,538,160 | 39,591 |
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