UQCC6 ubiquinol-cytochrome c reductase complex assembly factor 6
Information
- Symbol
- UQCC6
- Type
- protein-coding
- Description
- ubiquinol-cytochrome c reductase complex assembly factor 6
- Entrez Gene ID
- 728568
- Genome
- hg19
- Position
- chr12:104,343,972-104,350,993
- Genome
- hg38
- Position
- chr12:103,950,194-103,957,215
- MIM
- 618812 OMIM
- HGNC
- HGNC:34450 HGNC
- Ensembl
- ENSG00000204954 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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0 |
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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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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 | |||
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | BR |
SYNONYM | BRAWNIN |
SYNONYM | C12orf73 |
MIM | 618812 OMIM |
HGNC | HGNC:34450 HGNC |
Ensembl | ENSG00000204954 Ensembl |
AllianceGenome | HGNC:34450 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000546540.1 | hg38 | chr12 | 103,956,304 | 103,957,213 | 910 |
ENST00000547945.5 | hg38 | chr12 | 103,951,420 | 103,957,273 | 5,854 |
ENST00000553183.5 | hg38 | chr12 | 103,951,282 | 103,965,708 | 14,427 |
ENST00000546819.1 | hg38 | chr12 | 103,954,652 | 103,957,215 | 2,564 |
ENST00000549478.1 | hg38 | chr12 | 103,950,745 | 103,957,190 | 6,446 |
ENST00000378090.9 | hg38 | chr12 | 103,950,194 | 103,957,215 | 7,022 |
ENST00000552940.1 | hg38 | chr12 | 103,951,584 | 103,957,147 | 5,564 |
ENST00000547975.5 | hg38 | chr12 | 103,950,740 | 103,957,181 | 6,442 |
ENST00000378090.9 | hg19 | chr12 | 104,343,972 | 104,350,993 | 7,022 |
ENST00000547975.5 | hg19 | chr12 | 104,344,518 | 104,350,959 | 6,442 |
ENST00000549478.1 | hg19 | chr12 | 104,344,523 | 104,350,968 | 6,446 |
ENST00000553183.5 | hg19 | chr12 | 104,345,060 | 104,359,486 | 14,427 |
ENST00000547945.5 | hg19 | chr12 | 104,345,198 | 104,351,051 | 5,854 |
ENST00000552940.1 | hg19 | chr12 | 104,345,362 | 104,350,925 | 5,564 |
ENST00000546819.1 | hg19 | chr12 | 104,348,430 | 104,350,993 | 2,564 |
ENST00000546540.1 | hg19 | chr12 | 104,350,082 | 104,350,991 | 910 |
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