GPN3 GPN-loop GTPase 3
Information
- Symbol
- GPN3
- Type
- protein-coding
- Description
- GPN-loop GTPase 3
- Entrez Gene ID
- 51184
- Genome
- hg19
- Position
- chr12:110,890,292-110,906,526
- Genome
- hg38
- Position
- chr12:110,452,487-110,468,721
- HGNC
- HGNC:30186 HGNC
- Ensembl
- ENSG00000111231 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 20 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
20 |
 |
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
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
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| 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 | ATPBD1C |
| HGNC | HGNC:30186 HGNC |
| Ensembl | ENSG00000111231 Ensembl |
| AllianceGenome | HGNC:30186 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000537466.6 | hg38 | chr12 | 110,452,489 | 110,468,264 | 15,776 |
| ENST00000543199.5 | hg38 | chr12 | 110,452,487 | 110,468,721 | 16,235 |
| ENST00000228827.8 | hg38 | chr12 | 110,452,486 | 110,468,257 | 15,772 |
| ENST00000228827.8 | hg19 | chr12 | 110,890,291 | 110,906,062 | 15,772 |
| ENST00000543199.5 | hg19 | chr12 | 110,890,292 | 110,906,526 | 16,235 |
| ENST00000537466.6 | hg19 | chr12 | 110,890,294 | 110,906,069 | 15,776 |
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