RGPD4 RANBP2 like and GRIP domain containing 4
Information
- Symbol
- RGPD4
- Type
- protein-coding
- Description
- RANBP2 like and GRIP domain containing 4
- Entrez Gene ID
- 285190
- Genome
- hg19
- Position
- chr2:108,443,348-108,509,000
- Genome
- hg38
- Position
- chr2:107,826,892-107,892,544
- MIM
- 612707 OMIM
- HGNC
- HGNC:32417 HGNC
- Ensembl
- ENSG00000196862 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 38 |
not provided | 2 | 2 |
Uncertain significance | 0 | 262 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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302 |
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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
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 | : | |
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 |
---|---|
SYNONYM | RGP4 |
MIM | 612707 OMIM |
HGNC | HGNC:32417 HGNC |
Ensembl | ENSG00000196862 Ensembl |
AllianceGenome | HGNC:32417 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000408999.4 | hg38 | chr2 | 107,826,892 | 107,892,544 | 65,653 |
ENST00000408999.4 | hg19 | chr2 | 108,443,348 | 108,509,000 | 65,653 |
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