MAP2K7 mitogen-activated protein kinase kinase 7
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 22 |
| Likely benign | 0 | 4 |
| other | 0 | 2 |
| Uncertain significance | 0 | 36 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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62 |
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2 |
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 | |||||||||||
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | JNKK2 |
| SYNONYM | MAPKK7 |
| SYNONYM | MEK |
| SYNONYM | MEK 7 |
| SYNONYM | MKK7 |
| SYNONYM | PRKMK7 |
| SYNONYM | SAPKK-4 |
| SYNONYM | SAPKK4 |
| MIM | 603014 OMIM |
| HGNC | HGNC:6847 HGNC |
| Ensembl | ENSG00000076984 Ensembl |
| AllianceGenome | HGNC:6847 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000397983.7 | hg38 | chr19 | 7,903,885 | 7,914,459 | 10,575 |
| ENST00000397981.7 | hg38 | chr19 | 7,903,843 | 7,914,478 | 10,636 |
| ENST00000397979.4 | hg38 | chr19 | 7,903,877 | 7,914,478 | 10,602 |
| ENST00000397981.7 | hg19 | chr19 | 7,968,728 | 7,979,363 | 10,636 |
| ENST00000397979.4 | hg19 | chr19 | 7,968,762 | 7,979,363 | 10,602 |
| ENST00000397983.7 | hg19 | chr19 | 7,968,770 | 7,979,344 | 10,575 |
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