TMEM132D-AS1 TMEM132D antisense RNA 1
Information
- Symbol
- TMEM132D-AS1
- Type
- ncRNA
- Description
- TMEM132D antisense RNA 1
- Entrez Gene ID
- 283352
- Genome
- hg19
- Position
- chr12:129,594,244-129,597,838
- Genome
- hg38
- Position
- chr12:129,109,699-129,113,293
- HGNC
- HGNC:27466 HGNC
- Ensembl
- ENSG00000249196 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar |
|---|
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
0 |
 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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| Filtering | : |
| Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000542535.5 | hg38 | chr12 | 129,109,693 | 129,113,294 | 3,602 |
| ENST00000510001.6 | hg38 | chr12 | 129,109,695 | 129,113,294 | 3,600 |
| ENST00000537367.5 | hg38 | chr12 | 129,109,699 | 129,113,293 | 3,595 |
| ENST00000541320.5 | hg38 | chr12 | 129,109,695 | 129,113,294 | 3,600 |
| ENST00000542535.5 | hg19 | chr12 | 129,594,238 | 129,597,839 | 3,602 |
| ENST00000510001.6 | hg19 | chr12 | 129,594,240 | 129,597,839 | 3,600 |
| ENST00000541320.5 | hg19 | chr12 | 129,594,240 | 129,597,839 | 3,600 |
| ENST00000537367.5 | hg19 | chr12 | 129,594,244 | 129,597,838 | 3,595 |
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