RCHY1 ring finger and CHY zinc finger domain containing 1
Information
- Symbol
- RCHY1
- Type
- protein-coding
- Description
- ring finger and CHY zinc finger domain containing 1
- Entrez Gene ID
- 25898
- Genome
- hg19
- Position
- chr4:76,404,243-76,439,613
- Genome
- hg38
- Position
- chr4:75,479,033-75,514,403
- MIM
- 607680 OMIM
- HGNC
- HGNC:17479 HGNC
- Ensembl
- ENSG00000163743 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 8 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
12 |
 |
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 | ARNIP |
| SYNONYM | CHIMP |
| SYNONYM | PIRH2 |
| SYNONYM | PRO1996 |
| SYNONYM | RNF199 |
| SYNONYM | ZCHY |
| SYNONYM | ZNF363 |
| MIM | 607680 OMIM |
| HGNC | HGNC:17479 HGNC |
| Ensembl | ENSG00000163743 Ensembl |
| AllianceGenome | HGNC:17479 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000507014.1 | hg38 | chr4 | 75,482,538 | 75,514,297 | 31,760 |
| ENST00000380840.6 | hg38 | chr4 | 75,481,469 | 75,514,286 | 32,818 |
| ENST00000512706.5 | hg38 | chr4 | 75,482,413 | 75,514,430 | 32,018 |
| ENST00000513257.5 | hg38 | chr4 | 75,482,538 | 75,514,286 | 31,749 |
| ENST00000324439.10 | hg38 | chr4 | 75,479,033 | 75,514,403 | 35,371 |
| ENST00000324439.10 | hg19 | chr4 | 76,404,243 | 76,439,613 | 35,371 |
| ENST00000380840.6 | hg19 | chr4 | 76,406,679 | 76,439,496 | 32,818 |
| ENST00000512706.5 | hg19 | chr4 | 76,407,623 | 76,439,640 | 32,018 |
| ENST00000513257.5 | hg19 | chr4 | 76,407,748 | 76,439,496 | 31,749 |
| ENST00000507014.1 | hg19 | chr4 | 76,407,748 | 76,439,507 | 31,760 |
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