TRIM51 tripartite motif-containing 51
Information
- Symbol
- TRIM51
- Type
- protein-coding
- Description
- tripartite motif-containing 51
- Entrez Gene ID
- 84767
- Genome
- hg19
- Position
- chr11:55,650,773-55,659,286
- Genome
- hg38
- Position
- chr11:55,883,297-55,891,810
- HGNC
- HGNC:19023 HGNC
- Ensembl
- ENSG00000124900 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Uncertain significance | 0 | 54 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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56 |
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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 |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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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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 |
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SYNONYM | SPRYD5 |
SYNONYM | TRIM51A |
HGNC | HGNC:19023 HGNC |
Ensembl | ENSG00000124900 Ensembl |
AllianceGenome | HGNC:19023 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000449290.6 | hg38 | chr11 | 55,883,297 | 55,891,810 | 8,514 |
ENST00000244891.3 | hg38 | chr11 | 55,885,920 | 55,891,810 | 5,891 |
ENST00000449290.6 | hg19 | chr11 | 55,650,773 | 55,659,286 | 8,514 |
ENST00000244891.3 | hg19 | chr11 | 55,653,396 | 55,659,286 | 5,891 |
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