TEPSIN TEPSIN adaptor related protein complex 4 accessory protein
Information
- Symbol
- TEPSIN
- Type
- protein-coding
- Description
- TEPSIN adaptor related protein complex 4 accessory protein
- Entrez Gene ID
- 146705
- Genome
- hg19
- Position
- chr17:79,202,077-79,212,855
- Genome
- hg38
- Position
- chr17:81,228,277-81,239,055
- HGNC
- HGNC:26458 HGNC
- Ensembl
- ENSG00000167302 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 10 |
Uncertain significance | 0 | 16 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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32 |
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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 |
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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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 | C17orf56 |
SYNONYM | ENTHD2 |
HGNC | HGNC:26458 HGNC |
Ensembl | ENSG00000167302 Ensembl |
AllianceGenome | HGNC:26458 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000637944.2 | hg38 | chr17 | 81,228,277 | 81,239,055 | 10,779 |
ENST00000300714.7 | hg38 | chr17 | 81,228,277 | 81,239,091 | 10,815 |
ENST00000637944.2 | hg19 | chr17 | 79,202,077 | 79,212,855 | 10,779 |
ENST00000300714.7 | hg19 | chr17 | 79,202,077 | 79,212,891 | 10,815 |
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