MOK MOK protein kinase
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 6 |
Uncertain significance | 0 | 80 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
88 |
![]() |
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
|
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 | RAGE |
SYNONYM | RAGE-1 |
SYNONYM | RAGE1 |
SYNONYM | STK30 |
MIM | 605762 OMIM |
HGNC | HGNC:9833 HGNC |
Ensembl | ENSG00000080823 Ensembl |
AllianceGenome | HGNC:9833 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000522534.5 | hg38 | chr14 | 102,229,267 | 102,238,446 | 9,180 |
ENST00000522874.5 | hg38 | chr14 | 102,228,839 | 102,305,151 | 76,313 |
ENST00000561150.5 | hg38 | chr14 | 102,226,140 | 102,235,424 | 9,285 |
ENST00000361847.7 | hg38 | chr14 | 102,228,836 | 102,305,164 | 76,329 |
ENST00000519058.5 | hg38 | chr14 | 102,229,120 | 102,246,159 | 17,040 |
ENST00000523231.5 | hg38 | chr14 | 102,228,839 | 102,240,597 | 11,759 |
ENST00000524214.5 | hg38 | chr14 | 102,229,137 | 102,305,185 | 76,049 |
ENST00000524370.5 | hg38 | chr14 | 102,228,839 | 102,240,611 | 11,773 |
ENST00000522867.1 | hg38 | chr14 | 102,228,886 | 102,235,435 | 6,550 |
ENST00000517966.5 | hg38 | chr14 | 102,228,831 | 102,240,621 | 11,791 |
ENST00000517966.5 | hg19 | chr14 | 102,695,168 | 102,706,958 | 11,791 |
ENST00000361847.7 | hg19 | chr14 | 102,695,173 | 102,771,501 | 76,329 |
ENST00000519058.5 | hg19 | chr14 | 102,695,457 | 102,712,496 | 17,040 |
ENST00000522534.5 | hg19 | chr14 | 102,695,604 | 102,704,783 | 9,180 |
ENST00000523231.5 | hg19 | chr14 | 102,695,176 | 102,706,934 | 11,759 |
ENST00000561150.5 | hg19 | chr14 | 102,692,477 | 102,701,761 | 9,285 |
ENST00000524370.5 | hg19 | chr14 | 102,695,176 | 102,706,948 | 11,773 |
ENST00000522874.5 | hg19 | chr14 | 102,695,176 | 102,771,488 | 76,313 |
ENST00000522867.1 | hg19 | chr14 | 102,695,223 | 102,701,772 | 6,550 |
ENST00000524214.5 | hg19 | chr14 | 102,695,474 | 102,771,522 | 76,049 |
Genome browser