MAPK3 mitogen-activated protein kinase 3
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely pathogenic | 0 | 2 |
Benign | 0 | 4 |
Likely benign | 0 | 22 |
not provided | 14 | 0 |
Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
4 |
![]() |
42 |
![]() |
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
|
Category | : |
|
Search word | : | |
Filtering | : |
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
|
Category | : |
|
Search word | : | |
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
|
Category | : |
|
Search word | : | |
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 | ERK-1 |
SYNONYM | ERK1 |
SYNONYM | ERT2 |
SYNONYM | HS44KDAP |
SYNONYM | HUMKER1A |
SYNONYM | P44ERK1 |
SYNONYM | P44MAPK |
SYNONYM | PRKM3 |
SYNONYM | p44-ERK1 |
SYNONYM | p44-MAPK |
MIM | 601795 OMIM |
HGNC | HGNC:6877 HGNC |
Ensembl | ENSG00000102882 Ensembl |
AllianceGenome | HGNC:6877 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000322266.9 | hg38 | chr16 | 30,114,106 | 30,123,309 | 9,204 |
ENST00000395200.5 | hg38 | chr16 | 30,116,635 | 30,123,150 | 6,516 |
ENST00000395202.5 | hg38 | chr16 | 30,116,668 | 30,123,209 | 6,542 |
ENST00000484663.5 | hg38 | chr16 | 30,114,106 | 30,122,968 | 8,863 |
ENST00000395199.7 | hg38 | chr16 | 30,116,837 | 30,123,209 | 6,373 |
ENST00000263025.9 | hg38 | chr16 | 30,114,105 | 30,123,220 | 9,116 |
ENST00000263025.9 | hg19 | chr16 | 30,125,426 | 30,134,541 | 9,116 |
ENST00000484663.5 | hg19 | chr16 | 30,125,427 | 30,134,289 | 8,863 |
ENST00000322266.9 | hg19 | chr16 | 30,125,427 | 30,134,630 | 9,204 |
ENST00000395200.5 | hg19 | chr16 | 30,127,956 | 30,134,471 | 6,516 |
ENST00000395202.5 | hg19 | chr16 | 30,127,989 | 30,134,530 | 6,542 |
ENST00000395199.7 | hg19 | chr16 | 30,128,158 | 30,134,530 | 6,373 |
Genome browser