ZBTB7B zinc finger and BTB domain containing 7B
Information
- Symbol
- ZBTB7B
- Type
- protein-coding
- Description
- zinc finger and BTB domain containing 7B
- Entrez Gene ID
- 51043
- Genome
- hg19
- Position
- chr1:154,975,106-154,990,998
- Genome
- hg38
- Position
- chr1:155,002,630-155,018,522
- MIM
- 607646 OMIM
- HGNC
- HGNC:18668 HGNC
- Ensembl
- ENSG00000160685 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 8 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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2 |
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10 |
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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 | |||||
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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 | |||
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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 | CKROX |
SYNONYM | THPOK |
SYNONYM | ZBTB15 |
SYNONYM | ZFP-67 |
SYNONYM | ZFP67 |
SYNONYM | ZNF857B |
SYNONYM | c-KROX |
SYNONYM | hcKROX |
SYNONYM | vGAF |
MIM | 607646 OMIM |
HGNC | HGNC:18668 HGNC |
Ensembl | ENSG00000160685 Ensembl |
AllianceGenome | HGNC:18668 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000368426.3 | hg38 | chr1 | 155,002,657 | 155,018,522 | 15,866 |
ENST00000292176.2 | hg38 | chr1 | 155,014,448 | 155,016,981 | 2,534 |
ENST00000417934.6 | hg38 | chr1 | 155,002,630 | 155,018,522 | 15,893 |
ENST00000535420.6 | hg38 | chr1 | 155,002,802 | 155,018,523 | 15,722 |
ENST00000417934.6 | hg19 | chr1 | 154,975,106 | 154,990,998 | 15,893 |
ENST00000368426.3 | hg19 | chr1 | 154,975,133 | 154,990,998 | 15,866 |
ENST00000535420.6 | hg19 | chr1 | 154,975,278 | 154,990,999 | 15,722 |
ENST00000292176.2 | hg19 | chr1 | 154,986,924 | 154,989,457 | 2,534 |
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