TVP23B trans-golgi network vesicle protein 23 homolog B
Information
- Symbol
- TVP23B
- Type
- protein-coding
- Description
- trans-golgi network vesicle protein 23 homolog B
- Entrez Gene ID
- 51030
- Genome
- hg19
- Position
- chr17:18,684,496-18,710,027
- Genome
- hg38
- Position
- chr17:18,781,183-18,806,714
- HGNC
- HGNC:20399 HGNC
- Ensembl
- ENSG00000171928 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| not provided | 2 | 0 |
| Uncertain significance | 0 | 22 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
22 |
 |
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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| 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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| 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 | CGI-148 |
| SYNONYM | FAM18B |
| SYNONYM | FAM18B1 |
| SYNONYM | NPD008 |
| SYNONYM | YDR084C |
| HGNC | HGNC:20399 HGNC |
| Ensembl | ENSG00000171928 Ensembl |
| AllianceGenome | HGNC:20399 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000581733.1 | hg38 | chr17 | 18,789,035 | 18,806,202 | 17,168 |
| ENST00000476139.5 | hg38 | chr17 | 18,781,314 | 18,806,714 | 25,401 |
| ENST00000574226.5 | hg38 | chr17 | 18,781,155 | 18,804,616 | 23,462 |
| ENST00000307767.13 | hg38 | chr17 | 18,781,183 | 18,806,714 | 25,532 |
| ENST00000574226.5 | hg19 | chr17 | 18,684,468 | 18,707,929 | 23,462 |
| ENST00000307767.13 | hg19 | chr17 | 18,684,496 | 18,710,027 | 25,532 |
| ENST00000476139.5 | hg19 | chr17 | 18,684,627 | 18,710,027 | 25,401 |
| ENST00000581733.1 | hg19 | chr17 | 18,692,348 | 18,709,515 | 17,168 |
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