RRAD RRAD, Ras related glycolysis inhibitor and calcium channel regulator
Information
- Symbol
- RRAD
- Type
- protein-coding
- Description
- RRAD, Ras related glycolysis inhibitor and calcium channel regulator
- Entrez Gene ID
- 6236
- Genome
- hg19
- Position
- chr16:66,955,588-66,959,438
- Genome
- hg38
- Position
- chr16:66,921,685-66,925,535
- MIM
- 179503 OMIM
- HGNC
- HGNC:10446 HGNC
- Ensembl
- ENSG00000166592 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 30 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
30 |
 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
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MGeND data only
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| 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
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| Category | : |
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| 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 | RAD |
| SYNONYM | RAD1 |
| SYNONYM | REM3 |
| MIM | 179503 OMIM |
| HGNC | HGNC:10446 HGNC |
| Ensembl | ENSG00000166592 Ensembl |
| AllianceGenome | HGNC:10446 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000299759.11 | hg38 | chr16 | 66,921,685 | 66,925,535 | 3,851 |
| ENST00000299759.11 | hg19 | chr16 | 66,955,588 | 66,959,438 | 3,851 |
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