COX20 cytochrome c oxidase assembly factor COX20
Information
- Symbol
- COX20
- Type
- protein-coding
- Description
- cytochrome c oxidase assembly factor COX20
- Entrez Gene ID
- 116228
- Genome
- hg19
- Position
- chr1:244,998,918-245,006,554
- Genome
- hg38
- Position
- chr1:244,835,616-244,843,252
- MIM
- 614698 OMIM
- HGNC
- HGNC:26970 HGNC
- Ensembl
- ENSG00000203667 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 14 |
Likely pathogenic | 0 | 6 |
Benign | 0 | 28 |
Likely benign | 0 | 88 |
Conflicting classifications of pathogenicity | 0 | 12 |
not provided | 1 | 0 |
Uncertain significance | 0 | 78 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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44 |
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154 |
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12 |
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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Search word | : | |
Filtering | : |
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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 | FAM36A |
SYNONYM | MC4DN11 |
MIM | 614698 OMIM |
HGNC | HGNC:26970 HGNC |
Ensembl | ENSG00000203667 Ensembl |
AllianceGenome | HGNC:26970 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000411948.7 | hg38 | chr1 | 244,835,658 | 244,845,057 | 9,400 |
ENST00000366528.3 | hg38 | chr1 | 244,835,616 | 244,843,252 | 7,637 |
ENST00000366528.3 | hg19 | chr1 | 244,998,918 | 245,006,554 | 7,637 |
ENST00000411948.7 | hg19 | chr1 | 244,998,960 | 245,008,359 | 9,400 |
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