ATP6V0E2 ATPase H+ transporting V0 subunit e2
Information
- Symbol
- ATP6V0E2
- Type
- protein-coding
- Description
- ATPase H+ transporting V0 subunit e2
- Entrez Gene ID
- 155066
- Genome
- hg19
- Position
- chr7:149,571,065-149,577,778
- Genome
- hg38
- Position
- chr7:149,873,976-149,880,689
- MIM
- 611019 OMIM
- HGNC
- HGNC:21723 HGNC
- Ensembl
- ENSG00000171130 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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| 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
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | ATP6V0E2L |
| SYNONYM | C7orf32 |
| MIM | 611019 OMIM |
| HGNC | HGNC:21723 HGNC |
| Ensembl | ENSG00000171130 Ensembl |
| AllianceGenome | HGNC:21723 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000421974.7 | hg38 | chr7 | 149,872,968 | 149,880,689 | 7,722 |
| ENST00000425642.3 | hg38 | chr7 | 149,873,969 | 149,880,695 | 6,727 |
| ENST00000606024.5 | hg38 | chr7 | 149,873,987 | 149,879,996 | 6,010 |
| ENST00000456496.7 | hg38 | chr7 | 149,872,968 | 149,880,693 | 7,726 |
| ENST00000464662.5 | hg38 | chr7 | 149,873,993 | 149,878,965 | 4,973 |
| ENST00000479613.5 | hg38 | chr7 | 149,873,976 | 149,880,689 | 6,714 |
| ENST00000421974.7 | hg19 | chr7 | 149,570,057 | 149,577,778 | 7,722 |
| ENST00000456496.7 | hg19 | chr7 | 149,570,057 | 149,577,782 | 7,726 |
| ENST00000425642.3 | hg19 | chr7 | 149,571,058 | 149,577,784 | 6,727 |
| ENST00000479613.5 | hg19 | chr7 | 149,571,065 | 149,577,778 | 6,714 |
| ENST00000606024.5 | hg19 | chr7 | 149,571,076 | 149,577,085 | 6,010 |
| ENST00000464662.5 | hg19 | chr7 | 149,571,082 | 149,576,054 | 4,973 |
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