TMEM121B transmembrane protein 121B
Information
- Symbol
- TMEM121B
- Type
- protein-coding
- Description
- transmembrane protein 121B
- Entrez Gene ID
- 27439
- Genome
- hg19
- Position
- chr22:17,597,187-17,602,250
- Genome
- hg38
- Position
- chr22:17,116,297-17,121,360
- HGNC
- HGNC:1844 HGNC
- Ensembl
- ENSG00000183307 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 84 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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86 |
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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 |
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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000331437.4 | hg38 | chr22 | 17,116,297 | 17,121,360 | 5,064 |
ENST00000399875.1 | hg38 | chr22 | 17,116,299 | 17,121,367 | 5,069 |
ENST00000331437.4 | hg19 | chr22 | 17,597,187 | 17,602,250 | 5,064 |
ENST00000399875.1 | hg19 | chr22 | 17,597,189 | 17,602,257 | 5,069 |
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