TSGA10IP testis specific 10 interacting protein
Information
- Symbol
- TSGA10IP
- Type
- protein-coding
- Description
- testis specific 10 interacting protein
- Entrez Gene ID
- 254187
- Genome
- hg19
- Position
- chr11:65,712,951-65,727,437
- Genome
- hg38
- Position
- chr11:65,945,480-65,959,966
- HGNC
- HGNC:26555 HGNC
- Ensembl
- ENSG00000175513 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 12 |
Uncertain significance | 0 | 88 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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100 |
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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
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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 |
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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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Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | FAM161C |
HGNC | HGNC:26555 HGNC |
Ensembl | ENSG00000175513 Ensembl |
AllianceGenome | HGNC:26555 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000532620.6 | hg38 | chr11 | 65,945,480 | 65,959,966 | 14,487 |
ENST00000532620.6 | hg19 | chr11 | 65,712,951 | 65,727,437 | 14,487 |
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