STK17B serine/threonine kinase 17b
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 22 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
22 |
![]() |
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 | DRAK2 |
MIM | 604727 OMIM |
HGNC | HGNC:11396 HGNC |
Ensembl | ENSG00000081320 Ensembl |
AllianceGenome | HGNC:11396 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000409228.5 | hg38 | chr2 | 196,137,447 | 196,176,503 | 39,057 |
ENST00000420683.2 | hg38 | chr2 | 196,133,583 | 196,176,327 | 42,745 |
ENST00000449152.2 | hg38 | chr2 | 196,133,583 | 196,171,000 | 37,418 |
ENST00000606789.2 | hg38 | chr2 | 196,155,267 | 196,171,578 | 16,312 |
ENST00000263955.9 | hg38 | chr2 | 196,133,583 | 196,171,578 | 37,996 |
ENST00000714422.1 | hg38 | chr2 | 196,161,055 | 196,171,555 | 10,501 |
ENST00000714423.1 | hg38 | chr2 | 196,162,170 | 196,171,578 | 9,409 |
ENST00000714417.1 | hg38 | chr2 | 196,135,869 | 196,171,319 | 35,451 |
ENST00000449152.2 | hg19 | chr2 | 196,998,307 | 197,035,724 | 37,418 |
ENST00000263955.9 | hg19 | chr2 | 196,998,307 | 197,036,302 | 37,996 |
ENST00000420683.2 | hg19 | chr2 | 196,998,307 | 197,041,051 | 42,745 |
ENST00000714417.1 | hg19 | chr2 | 197,000,593 | 197,036,043 | 35,451 |
ENST00000409228.5 | hg19 | chr2 | 197,002,171 | 197,041,227 | 39,057 |
ENST00000606789.2 | hg19 | chr2 | 197,019,991 | 197,036,302 | 16,312 |
ENST00000714422.1 | hg19 | chr2 | 197,025,779 | 197,036,279 | 10,501 |
ENST00000714423.1 | hg19 | chr2 | 197,026,894 | 197,036,302 | 9,409 |
Genome browser