RGPD5 RANBP2 like and GRIP domain containing 5
Information
- Symbol
- RGPD5
- Type
- protein-coding
- Description
- RANBP2 like and GRIP domain containing 5
- Entrez Gene ID
- 84220
- Genome
- hg19
- Position
- chr2:110,551,882-110,615,282
- Genome
- hg38
- Position
- chr2:109,794,305-109,857,705
- MIM
- 612708 OMIM
- HGNC
- HGNC:32418 HGNC
- Ensembl
- ENSG00000015568 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
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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
[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 |
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | BS-63 |
SYNONYM | BS63 |
SYNONYM | HEL161 |
SYNONYM | RGP5 |
MIM | 612708 OMIM |
HGNC | HGNC:32418 HGNC |
Ensembl | ENSG00000015568 Ensembl |
AllianceGenome | HGNC:32418 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000016946.8 | hg38 | chr2 | 109,794,305 | 109,857,705 | 63,401 |
ENST00000272454.10 | hg38 | chr2 | 109,794,274 | 109,832,963 | 38,690 |
ENST00000393283.5 | hg38 | chr2 | 109,792,758 | 109,833,019 | 40,262 |
ENST00000393283.5 | hg19 | chr2 | 110,550,335 | 110,590,596 | 40,262 |
ENST00000272454.10 | hg19 | chr2 | 110,551,851 | 110,590,540 | 38,690 |
ENST00000016946.8 | hg19 | chr2 | 110,551,882 | 110,615,282 | 63,401 |
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