TMEM132E-DT TMEM132E divergent transcript
Information
- Symbol
- TMEM132E-DT
- Type
- ncRNA
- Description
- TMEM132E divergent transcript
- Entrez Gene ID
- 400591
- Genome
- hg19
- Position
- chr17:32,901,142-32,906,388
- Genome
- hg38
- Position
- chr17:34,574,123-34,579,369
- HGNC
- HGNC:34412 HGNC
- Ensembl
- ENSG00000197322 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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0 |
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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 |
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SYNONYM | C17orf102 |
HGNC | HGNC:34412 HGNC |
Ensembl | ENSG00000197322 Ensembl |
AllianceGenome | HGNC:34412 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000623254.1 | hg38 | chr17 | 34,574,123 | 34,579,369 | 5,247 |
ENST00000661426.1 | hg38 | chr17 | 34,574,368 | 34,579,149 | 4,782 |
ENST00000623254.1 | hg19 | chr17 | 32,901,142 | 32,906,388 | 5,247 |
ENST00000661426.1 | hg19 | chr17 | 32,901,387 | 32,906,168 | 4,782 |
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