TNFAIP8L3 TNF alpha induced protein 8 like 3
Information
- Symbol
- TNFAIP8L3
- Type
- protein-coding
- Description
- TNF alpha induced protein 8 like 3
- Entrez Gene ID
- 388121
- Genome
- hg19
- Position
- chr15:51,348,795-51,397,473
- Genome
- hg38
- Position
- chr15:51,056,598-51,105,276
- MIM
- 616438 OMIM
- HGNC
- HGNC:20620 HGNC
- Ensembl
- ENSG00000183578 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 42 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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46 |
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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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Category | : |
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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 |
---|---|
SYNONYM | TIPE3 |
MIM | 616438 OMIM |
HGNC | HGNC:20620 HGNC |
Ensembl | ENSG00000183578 Ensembl |
AllianceGenome | HGNC:20620 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000649177.1 | hg38 | chr15 | 51,056,677 | 51,094,501 | 37,825 |
ENST00000637513.2 | hg38 | chr15 | 51,056,601 | 51,094,906 | 38,306 |
ENST00000327536.5 | hg38 | chr15 | 51,056,598 | 51,105,276 | 48,679 |
ENST00000327536.5 | hg19 | chr15 | 51,348,795 | 51,397,473 | 48,679 |
ENST00000637513.2 | hg19 | chr15 | 51,348,798 | 51,387,103 | 38,306 |
ENST00000649177.1 | hg19 | chr15 | 51,348,874 | 51,386,698 | 37,825 |
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