TMEM116 transmembrane protein 116
Information
- Symbol
- TMEM116
- Type
- protein-coding
- Description
- transmembrane protein 116
- Entrez Gene ID
- 89894
- Genome
- hg19
- Position
- chr12:112,369,102-112,450,969
- Genome
- hg38
- Position
- chr12:111,931,298-112,013,165
- HGNC
- HGNC:25084 HGNC
- Ensembl
- ENSG00000198270 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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26 |
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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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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000552374.7 | hg38 | chr12 | 111,931,298 | 112,013,165 | 81,868 |
ENST00000355445.7 | hg38 | chr12 | 111,931,298 | 112,013,139 | 81,842 |
ENST00000549537.6 | hg38 | chr12 | 111,931,370 | 112,013,135 | 81,766 |
ENST00000550831.7 | hg38 | chr12 | 111,931,282 | 112,013,125 | 81,844 |
ENST00000355445.7 | hg19 | chr12 | 112,369,102 | 112,450,943 | 81,842 |
ENST00000550831.7 | hg19 | chr12 | 112,369,086 | 112,450,929 | 81,844 |
ENST00000549537.6 | hg19 | chr12 | 112,369,174 | 112,450,939 | 81,766 |
ENST00000552374.7 | hg19 | chr12 | 112,369,102 | 112,450,969 | 81,868 |
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