PDE7B-AS1 PDE7B antisense RNA 1
Information
- Symbol
- PDE7B-AS1
- Type
- ncRNA
- Description
- PDE7B antisense RNA 1
- Entrez Gene ID
- 644135
- Genome
- hg19
- Position
- chr6:136,374,489-136,546,756
- Genome
- hg38
- Position
- chr6:136,053,351-136,225,618
- HGNC
- HGNC:56334 HGNC
- Ensembl
- ENSG00000237596 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 | |||||
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000576956.3 | hg38 | chr6 | 136,034,031 | 136,094,828 | 60,798 |
| ENST00000585946.5 | hg38 | chr6 | 136,095,960 | 136,191,875 | 95,916 |
| ENST00000626414.1 | hg38 | chr6 | 135,991,936 | 136,070,296 | 78,361 |
| ENST00000419926.3 | hg38 | chr6 | 136,043,852 | 136,072,827 | 28,976 |
| ENST00000413745.3 | hg38 | chr6 | 136,044,464 | 136,064,638 | 20,175 |
| ENST00000417643.5 | hg38 | chr6 | 136,094,715 | 136,225,595 | 130,881 |
| ENST00000655618.1 | hg38 | chr6 | 136,053,351 | 136,225,618 | 172,268 |
| ENST00000626414.1 | hg19 | chr6 | 136,313,074 | 136,391,434 | 78,361 |
| ENST00000576956.3 | hg19 | chr6 | 136,355,169 | 136,415,966 | 60,798 |
| ENST00000419926.3 | hg19 | chr6 | 136,364,990 | 136,393,965 | 28,976 |
| ENST00000413745.3 | hg19 | chr6 | 136,365,602 | 136,385,776 | 20,175 |
| ENST00000655618.1 | hg19 | chr6 | 136,374,489 | 136,546,756 | 172,268 |
| ENST00000417643.5 | hg19 | chr6 | 136,415,853 | 136,546,733 | 130,881 |
| ENST00000585946.5 | hg19 | chr6 | 136,417,098 | 136,513,013 | 95,916 |
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