IGF2BP2-AS1 IGF2BP2 antisense RNA 1
Information
- Symbol
- IGF2BP2-AS1
- Type
- ncRNA
- Description
- IGF2BP2 antisense RNA 1
- Entrez Gene ID
- 646600
- Genome
- hg19
- Position
- chr3:185,431,080-185,435,955
- Genome
- hg38
- Position
- chr3:185,713,292-185,718,167
- HGNC
- HGNC:32674 HGNC
- Ensembl
- ENSG00000163915 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely pathogenic | 1 | 0 |
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
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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| Search word | : | |
| 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 | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | C3orf65 |
| HGNC | HGNC:32674 HGNC |
| Ensembl | ENSG00000163915 Ensembl |
| AllianceGenome | HGNC:32674 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000296270.1 | hg38 | chr3 | 185,713,292 | 185,718,167 | 4,876 |
| ENST00000456447.5 | hg38 | chr3 | 185,713,252 | 185,729,787 | 16,536 |
| ENST00000456447.5 | hg19 | chr3 | 185,431,040 | 185,447,575 | 16,536 |
| ENST00000296270.1 | hg19 | chr3 | 185,431,080 | 185,435,955 | 4,876 |
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