STK25 serine/threonine kinase 25
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 8 |
Uncertain significance | 0 | 62 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
70 |
![]() |
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 | SOK1 |
SYNONYM | YSK1 |
MIM | 602255 OMIM |
HGNC | HGNC:11404 HGNC |
Ensembl | ENSG00000115694 Ensembl |
AllianceGenome | HGNC:11404 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000316586.9 | hg38 | chr2 | 241,492,670 | 241,508,584 | 15,915 |
ENST00000401869.5 | hg38 | chr2 | 241,495,019 | 241,508,362 | 13,344 |
ENST00000535007.5 | hg38 | chr2 | 241,494,707 | 241,508,695 | 13,989 |
ENST00000405883.7 | hg38 | chr2 | 241,495,022 | 241,508,556 | 13,535 |
ENST00000543554.5 | hg38 | chr2 | 241,494,707 | 241,509,572 | 14,866 |
ENST00000405585.5 | hg38 | chr2 | 241,495,249 | 241,508,584 | 13,336 |
ENST00000403346.7 | hg38 | chr2 | 241,495,017 | 241,508,688 | 13,672 |
ENST00000316586.9 | hg19 | chr2 | 242,432,085 | 242,447,999 | 15,915 |
ENST00000401869.5 | hg19 | chr2 | 242,434,434 | 242,447,777 | 13,344 |
ENST00000403346.7 | hg19 | chr2 | 242,434,432 | 242,448,103 | 13,672 |
ENST00000405585.5 | hg19 | chr2 | 242,434,664 | 242,447,999 | 13,336 |
ENST00000405883.7 | hg19 | chr2 | 242,434,437 | 242,447,971 | 13,535 |
ENST00000535007.5 | hg19 | chr2 | 242,434,122 | 242,448,110 | 13,989 |
ENST00000543554.5 | hg19 | chr2 | 242,434,122 | 242,448,987 | 14,866 |
Genome browser