TSKS testis specific serine kinase substrate
Information
- Symbol
- TSKS
- Type
- protein-coding
- Description
- testis specific serine kinase substrate
- Entrez Gene ID
- 60385
- Genome
- hg19
- Position
- chr19:50,243,017-50,266,563
- Genome
- hg38
- Position
- chr19:49,739,760-49,763,306
- MIM
- 608253 OMIM
- HGNC
- HGNC:30719 HGNC
- Ensembl
- ENSG00000126467 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
not provided | 1 | 0 |
Uncertain significance | 0 | 86 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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86 |
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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
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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 | PPP1R161 |
SYNONYM | STK22S1 |
SYNONYM | TSKS1 |
SYNONYM | TSSKS |
MIM | 608253 OMIM |
HGNC | HGNC:30719 HGNC |
Ensembl | ENSG00000126467 Ensembl |
AllianceGenome | HGNC:30719 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000246801.8 | hg38 | chr19 | 49,739,760 | 49,763,306 | 23,547 |
ENST00000358830.3 | hg38 | chr19 | 49,739,757 | 49,747,378 | 7,622 |
ENST00000358830.3 | hg19 | chr19 | 50,243,014 | 50,250,635 | 7,622 |
ENST00000246801.8 | hg19 | chr19 | 50,243,017 | 50,266,563 | 23,547 |
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