RHNO1 RAD9-HUS1-RAD1 interacting nuclear orphan 1
Information
- Symbol
- RHNO1
- Type
- protein-coding
- Description
- RAD9-HUS1-RAD1 interacting nuclear orphan 1
- Entrez Gene ID
- 83695
- Genome
- hg19
- Position
- chr12:2,986,389-2,998,690
- Genome
- hg38
- Position
- chr12:2,877,223-2,889,524
- MIM
- 614085 OMIM
- HGNC
- HGNC:28206 HGNC
- Ensembl
- ENSG00000171792 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 4 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
4 |
 |
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
| 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 |
|---|---|
| SYNONYM | C12orf32 |
| SYNONYM | HKMT1188 |
| SYNONYM | RHINO |
| MIM | 614085 OMIM |
| HGNC | HGNC:28206 HGNC |
| Ensembl | ENSG00000171792 Ensembl |
| AllianceGenome | HGNC:28206 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000618250.4 | hg38 | chr12 | 2,877,199 | 2,889,523 | 12,325 |
| ENST00000489288.7 | hg38 | chr12 | 2,877,223 | 2,889,524 | 12,302 |
| ENST00000461997.5 | hg38 | chr12 | 2,877,199 | 2,889,271 | 12,073 |
| ENST00000461997.5 | hg19 | chr12 | 2,986,365 | 2,998,437 | 12,073 |
| ENST00000618250.4 | hg19 | chr12 | 2,986,365 | 2,998,689 | 12,325 |
| ENST00000489288.7 | hg19 | chr12 | 2,986,389 | 2,998,690 | 12,302 |
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