TMEM263 transmembrane protein 263
Information
- Symbol
- TMEM263
- Type
- protein-coding
- Description
- transmembrane protein 263
- Entrez Gene ID
- 90488
- Genome
- hg19
- Position
- chr12:107,349,685-107,367,813
- Genome
- hg38
- Position
- chr12:106,955,907-106,974,035
- HGNC
- HGNC:28281 HGNC
- Ensembl
- ENSG00000151135 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 10 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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10 |
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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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Search word | : | |
Filtering | : |
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 | C12orf23 |
HGNC | HGNC:28281 HGNC |
Ensembl | ENSG00000151135 Ensembl |
AllianceGenome | HGNC:28281 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000547081.1 | hg38 | chr12 | 106,956,785 | 106,971,502 | 14,718 |
ENST00000548125.5 | hg38 | chr12 | 106,955,719 | 106,974,036 | 18,318 |
ENST00000280756.9 | hg38 | chr12 | 106,955,907 | 106,974,035 | 18,129 |
ENST00000550344.5 | hg38 | chr12 | 106,955,867 | 106,971,576 | 15,710 |
ENST00000547242.5 | hg38 | chr12 | 106,955,828 | 106,971,441 | 15,614 |
ENST00000551489.5 | hg38 | chr12 | 106,955,844 | 106,971,246 | 15,403 |
ENST00000551813.1 | hg38 | chr12 | 106,966,935 | 106,972,341 | 5,407 |
ENST00000548125.5 | hg19 | chr12 | 107,349,497 | 107,367,814 | 18,318 |
ENST00000547242.5 | hg19 | chr12 | 107,349,606 | 107,365,219 | 15,614 |
ENST00000551489.5 | hg19 | chr12 | 107,349,622 | 107,365,024 | 15,403 |
ENST00000550344.5 | hg19 | chr12 | 107,349,645 | 107,365,354 | 15,710 |
ENST00000280756.9 | hg19 | chr12 | 107,349,685 | 107,367,813 | 18,129 |
ENST00000547081.1 | hg19 | chr12 | 107,350,563 | 107,365,280 | 14,718 |
ENST00000551813.1 | hg19 | chr12 | 107,360,713 | 107,366,119 | 5,407 |
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