RGPD8 RANBP2 like and GRIP domain containing 8
Information
- Symbol
- RGPD8
- Type
- protein-coding
- Description
- RANBP2 like and GRIP domain containing 8
- Entrez Gene ID
- 727851
- Genome
- hg19
- Position
- chr2:113,125,946-113,191,222
- Genome
- hg38
- Position
- chr2:112,368,369-112,433,645
- MIM
- 602752 OMIM
- HGNC
- HGNC:9849 HGNC
- Ensembl
- ENSG00000169629 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 26 |
Uncertain significance | 0 | 146 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
174 |
![]() |
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
|
Category | : |
|
Search word | : | |
Filtering | : |
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
|
Category | : |
|
Search word | : | |
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
|
Category | : |
|
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 | RANBP2L1 |
SYNONYM | RGP8 |
SYNONYM | RanBP2alpha |
MIM | 602752 OMIM |
HGNC | HGNC:9849 HGNC |
Ensembl | ENSG00000169629 Ensembl |
AllianceGenome | HGNC:9849 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000330575.9 | hg38 | chr2 | 112,393,051 | 112,433,530 | 40,480 |
ENST00000409750.5 | hg38 | chr2 | 112,370,092 | 112,434,488 | 64,397 |
ENST00000302558.8 | hg38 | chr2 | 112,368,369 | 112,433,645 | 65,277 |
ENST00000302558.8 | hg19 | chr2 | 113,125,946 | 113,191,222 | 65,277 |
ENST00000409750.5 | hg19 | chr2 | 113,127,669 | 113,192,065 | 64,397 |
ENST00000330575.9 | hg19 | chr2 | 113,150,628 | 113,191,107 | 40,480 |
Genome browser