USP17L1 ubiquitin specific peptidase 17 like family member 1
Information
- Symbol
- USP17L1
- Type
- protein-coding
- Description
- ubiquitin specific peptidase 17 like family member 1
- Entrez Gene ID
- 401447
- Genome
- hg19
- Position
- chr8:7,189,909-7,191,501
- Genome
- hg38
- Position
- chr8:7,332,387-7,333,979
- HGNC
- HGNC:37182 HGNC
- Ensembl
- ENSG00000230549 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 8 |
not provided | 1 | 0 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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8 |
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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
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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | USP17L1P |
HGNC | HGNC:37182 HGNC |
Ensembl | ENSG00000230549 Ensembl |
AllianceGenome | HGNC:37182 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000529559.1 | hg38 | chr8 | 7,332,387 | 7,333,979 | 1,593 |
ENST00000529559.1 | hg19 | chr8 | 7,189,909 | 7,191,501 | 1,593 |
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