CCZ1B CCZ1 homolog B, vacuolar protein trafficking and biogenesis associated
Information
- Symbol
- CCZ1B
- Type
- protein-coding
- Description
- CCZ1 homolog B, vacuolar protein trafficking and biogenesis associated
- Entrez Gene ID
- 221960
- Genome
- hg19
- Position
- chr7:6,838,568-6,865,906
- Genome
- hg38
- Position
- chr7:6,798,937-6,826,275
- HGNC
- HGNC:21717 HGNC
- Ensembl
- ENSG00000146574 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 4 |
| Conflicting classifications of pathogenicity | 0 | 2 |
| Uncertain significance | 0 | 46 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
50 |
 |
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 | |||||||||||
Search Word
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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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| Category | : |
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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 | C7orf28A |
| SYNONYM | C7orf28B |
| SYNONYM | CCZ1 |
| SYNONYM | H_NH0577018.2 |
| HGNC | HGNC:21717 HGNC |
| Ensembl | ENSG00000146574 Ensembl |
| AllianceGenome | HGNC:21717 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000316731.13 | hg38 | chr7 | 6,798,937 | 6,826,275 | 27,339 |
| ENST00000626257.2 | hg38 | chr7 | 6,798,941 | 6,826,770 | 27,830 |
| ENST00000316731.13 | hg19 | chr7 | 6,838,568 | 6,865,906 | 27,339 |
| ENST00000626257.2 | hg19 | chr7 | 6,838,572 | 6,866,401 | 27,830 |
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