CHKB-CPT1B CHKB-CPT1B readthrough (NMD candidate)
Information
- Symbol
- CHKB-CPT1B
- Type
- ncRNA
- Description
- CHKB-CPT1B readthrough (NMD candidate)
- Entrez Gene ID
- 386593
- Genome
- hg19
- Position
- chr22:51,007,424-51,018,181
- Genome
- hg38
- Position
- chr22:50,568,995-50,579,752
- HGNC
- HGNC:41998 HGNC
- Ensembl
- ENSG00000254413 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| not provided | 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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| Category | : |
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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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| Category | : |
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| Search word | : | |
| 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 | CHKL-CPT1B |
| SYNONYM | CPT1-M |
| SYNONYM | CPT1B |
| SYNONYM | CPTI-M |
| HGNC | HGNC:41998 HGNC |
| Ensembl | ENSG00000254413 Ensembl |
| AllianceGenome | HGNC:41998 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000453634.5 | hg38 | chr22 | 50,568,995 | 50,579,752 | 10,758 |
| ENST00000453634.5 | hg19 | chr22 | 51,007,424 | 51,018,181 | 10,758 |
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