RNY1P9 RNY1 pseudogene 9
Information
- Symbol
- RNY1P9
- Type
- pseudo
- Description
- RNY1 pseudogene 9
- Entrez Gene ID
- 100874358
- Genome
- hg19
- Position
- chr22:20,829,490-20,829,598
- Genome
- hg38
- Position
- chr22:20,475,203-20,475,311
- HGNC
- HGNC:41481 HGNC
- Ensembl
- ENSG00000255156 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 15 | 0 |
Ranking
ClinVar | |
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Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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 | : | |
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | KLHL22-IT1 |
SYNONYM | RNYP1 |
HGNC | HGNC:41481 HGNC |
Ensembl | ENSG00000255156 Ensembl |
AllianceGenome | HGNC:41481 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000532431.1 | hg38 | chr22 | 20,475,203 | 20,475,311 | 109 |
ENST00000532431.1 | hg19 | chr22 | 20,829,490 | 20,829,598 | 109 |
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