RAD9B RAD9 checkpoint clamp component B
Information
- Symbol
- RAD9B
- Type
- protein-coding
- Description
- RAD9 checkpoint clamp component B
- Entrez Gene ID
- 144715
- Genome
- hg19
- Position
- chr12:110,940,044-110,969,891
- Genome
- hg38
- Position
- chr12:110,502,239-110,532,086
- MIM
- 608368 OMIM
- HGNC
- HGNC:21700 HGNC
- Ensembl
- ENSG00000151164 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 4 |
| Likely pathogenic | 0 | 11 |
| Benign | 0 | 2 |
| Likely benign | 0 | 10 |
| Uncertain significance | 0 | 30 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
42 |
 |
15 |
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
| 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 |
|---|---|
| MIM | 608368 OMIM |
| HGNC | HGNC:21700 HGNC |
| Ensembl | ENSG00000151164 Ensembl |
| AllianceGenome | HGNC:21700 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000409425.5 | hg38 | chr12 | 110,502,291 | 110,532,086 | 29,796 |
| ENST00000392672.8 | hg38 | chr12 | 110,502,239 | 110,532,086 | 29,848 |
| ENST00000409246.5 | hg38 | chr12 | 110,502,200 | 110,532,084 | 29,885 |
| ENST00000409300.6 | hg38 | chr12 | 110,502,331 | 110,533,556 | 31,226 |
| ENST00000409778.7 | hg38 | chr12 | 110,502,314 | 110,532,004 | 29,691 |
| ENST00000409246.5 | hg19 | chr12 | 110,940,005 | 110,969,889 | 29,885 |
| ENST00000392672.8 | hg19 | chr12 | 110,940,044 | 110,969,891 | 29,848 |
| ENST00000409425.5 | hg19 | chr12 | 110,940,096 | 110,969,891 | 29,796 |
| ENST00000409778.7 | hg19 | chr12 | 110,940,119 | 110,969,809 | 29,691 |
| ENST00000409300.6 | hg19 | chr12 | 110,940,136 | 110,971,361 | 31,226 |
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