UQCR10 ubiquinol-cytochrome c reductase, complex III subunit X
Information
- Symbol
- UQCR10
- Type
- protein-coding
- Description
- ubiquinol-cytochrome c reductase, complex III subunit X
- Entrez Gene ID
- 29796
- Genome
- hg19
- Position
- chr22:30,163,358-30,166,402
- Genome
- hg38
- Position
- chr22:29,767,369-29,770,413
- MIM
- 610843 OMIM
- HGNC
- HGNC:30863 HGNC
- Ensembl
- ENSG00000184076 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 10 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
10 |
 |
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 | HSPC051 |
| SYNONYM | HSPC119 |
| SYNONYM | HSPC151 |
| SYNONYM | QCR9 |
| SYNONYM | UCCR7.2 |
| SYNONYM | UCRC |
| MIM | 610843 OMIM |
| HGNC | HGNC:30863 HGNC |
| Ensembl | ENSG00000184076 Ensembl |
| AllianceGenome | HGNC:30863 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000401406.3 | hg38 | chr22 | 29,767,374 | 29,770,027 | 2,654 |
| ENST00000330029.6 | hg38 | chr22 | 29,767,369 | 29,770,413 | 3,045 |
| ENST00000330029.6 | hg19 | chr22 | 30,163,358 | 30,166,402 | 3,045 |
| ENST00000401406.3 | hg19 | chr22 | 30,163,363 | 30,166,016 | 2,654 |
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