ATP6V1G1 ATPase H+ transporting V1 subunit G1
Information
- Symbol
- ATP6V1G1
- Type
- protein-coding
- Description
- ATPase H+ transporting V1 subunit G1
- Entrez Gene ID
- 9550
- Genome
- hg19
- Position
- chr9:117,350,049-117,361,159
- Genome
- hg38
- Position
- chr9:114,587,769-114,598,879
- MIM
- 607296 OMIM
- HGNC
- HGNC:864 HGNC
- Ensembl
- ENSG00000136888 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely pathogenic | 1 | 0 |
| Uncertain significance | 0 | 14 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
14 |
 |
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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| Category | : |
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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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| 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 | ATP6G |
| SYNONYM | ATP6G1 |
| SYNONYM | ATP6GL |
| SYNONYM | ATP6J |
| SYNONYM | Vma10 |
| MIM | 607296 OMIM |
| HGNC | HGNC:864 HGNC |
| Ensembl | ENSG00000136888 Ensembl |
| AllianceGenome | HGNC:864 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000374050.4 | hg38 | chr9 | 114,587,769 | 114,598,879 | 11,111 |
| ENST00000677498.1 | hg38 | chr9 | 114,587,785 | 114,593,482 | 5,698 |
| ENST00000679150.1 | hg38 | chr9 | 114,587,839 | 114,597,743 | 9,905 |
| ENST00000677452.1 | hg38 | chr9 | 114,587,752 | 114,598,378 | 10,627 |
| ENST00000677115.1 | hg38 | chr9 | 114,587,706 | 114,598,384 | 10,679 |
| ENST00000677115.1 | hg19 | chr9 | 117,349,986 | 117,360,664 | 10,679 |
| ENST00000677452.1 | hg19 | chr9 | 117,350,032 | 117,360,658 | 10,627 |
| ENST00000374050.4 | hg19 | chr9 | 117,350,049 | 117,361,159 | 11,111 |
| ENST00000677498.1 | hg19 | chr9 | 117,350,065 | 117,355,762 | 5,698 |
| ENST00000679150.1 | hg19 | chr9 | 117,350,119 | 117,360,023 | 9,905 |
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