BDNF-AS BDNF antisense RNA
Clinical Significance
| MGeND | ClinVar |
|---|
Ranking
| ClinVar | |
|---|---|
 |
0 |
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0 |
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0 |
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0 |
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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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
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| 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 | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | ANTI-BDNF |
| SYNONYM | BDNF |
| SYNONYM | BDNF-AS1 |
| SYNONYM | BDNFAS |
| SYNONYM | BDNFOS |
| SYNONYM | NCRNA00049 |
| MIM | 611468 OMIM |
| HGNC | HGNC:20608 HGNC |
| Ensembl | ENSG00000245573 Ensembl |
| AllianceGenome | HGNC:20608 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000660080.1 | hg38 | chr11 | 27,639,943 | 27,696,422 | 56,480 |
| ENST00000652172.1 | hg38 | chr11 | 27,506,853 | 27,515,347 | 8,495 |
| ENST00000499568.3 | hg38 | chr11 | 27,506,852 | 27,698,171 | 191,320 |
| ENST00000651990.1 | hg38 | chr11 | 27,506,849 | 27,694,544 | 187,696 |
| ENST00000651742.1 | hg38 | chr11 | 27,506,847 | 27,677,805 | 170,959 |
| ENST00000499568.3 | hg19 | chr11 | 27,528,399 | 27,719,718 | 191,320 |
| ENST00000651742.1 | hg19 | chr11 | 27,528,394 | 27,699,352 | 170,959 |
| ENST00000651990.1 | hg19 | chr11 | 27,528,396 | 27,716,091 | 187,696 |
| ENST00000652172.1 | hg19 | chr11 | 27,528,400 | 27,536,894 | 8,495 |
| ENST00000660080.1 | hg19 | chr11 | 27,661,490 | 27,717,969 | 56,480 |
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