RGPD6 RANBP2 like and GRIP domain containing 6
Information
- Symbol
- RGPD6
- Type
- protein-coding
- Description
- RANBP2 like and GRIP domain containing 6
- Entrez Gene ID
- 729540
- Genome
- hg19
- Position
- chr2:111,271,379-111,334,799
- Genome
- hg38
- Position
- chr2:110,513,802-110,577,222
- MIM
- 612709 OMIM
- HGNC
- HGNC:32419 HGNC
- Ensembl
- ENSG00000183054 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 4 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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4 |
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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
[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 |
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 | RGP6 |
SYNONYM | RGPD7 |
SYNONYM | RanBP2L1 |
SYNONYM | RanBP2L2 |
MIM | 612709 OMIM |
HGNC | HGNC:32419 HGNC |
Ensembl | ENSG00000183054 Ensembl |
AllianceGenome | HGNC:32419 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000329516.8 | hg38 | chr2 | 110,513,802 | 110,577,222 | 63,421 |
ENST00000696446.1 | hg38 | chr2 | 110,513,802 | 110,577,222 | 63,421 |
ENST00000330331.9 | hg38 | chr2 | 110,538,488 | 110,577,101 | 38,614 |
ENST00000696448.1 | hg38 | chr2 | 110,513,963 | 110,610,840 | 96,878 |
ENST00000696446.1 | hg19 | chr2 | 111,271,379 | 111,334,799 | 63,421 |
ENST00000329516.8 | hg19 | chr2 | 111,271,379 | 111,334,799 | 63,421 |
ENST00000696448.1 | hg19 | chr2 | 111,271,540 | 111,368,417 | 96,878 |
ENST00000330331.9 | hg19 | chr2 | 111,296,065 | 111,334,678 | 38,614 |
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