C11orf54 chromosome 11 open reading frame 54
Information
- Symbol
- C11orf54
- Type
- protein-coding
- Description
- chromosome 11 open reading frame 54
- Entrez Gene ID
- 28970
- Genome
- hg19
- Position
- chr11:93,474,838-93,497,915
- Genome
- hg38
- Position
- chr11:93,741,672-93,764,749
- MIM
- 615810 OMIM
- HGNC
- HGNC:30204 HGNC
- Ensembl
- ENSG00000182919 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 2 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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2 |
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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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
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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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | MEEP |
SYNONYM | PTD012 |
SYNONYM | PTOD012 |
MIM | 615810 OMIM |
HGNC | HGNC:30204 HGNC |
Ensembl | ENSG00000182919 Ensembl |
AllianceGenome | HGNC:30204 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000331239.8 | hg38 | chr11 | 93,741,642 | 93,763,083 | 21,442 |
ENST00000540113.5 | hg38 | chr11 | 93,741,594 | 93,763,102 | 21,509 |
ENST00000528288.5 | hg38 | chr11 | 93,741,591 | 93,764,749 | 23,159 |
ENST00000528099.5 | hg38 | chr11 | 93,741,659 | 93,762,303 | 20,645 |
ENST00000354421.8 | hg38 | chr11 | 93,741,672 | 93,764,749 | 23,078 |
ENST00000617482.4 | hg38 | chr11 | 93,741,594 | 93,763,102 | 21,509 |
ENST00000528288.5 | hg19 | chr11 | 93,474,757 | 93,497,915 | 23,159 |
ENST00000617482.4 | hg19 | chr11 | 93,474,760 | 93,496,268 | 21,509 |
ENST00000540113.5 | hg19 | chr11 | 93,474,760 | 93,496,268 | 21,509 |
ENST00000331239.8 | hg19 | chr11 | 93,474,808 | 93,496,249 | 21,442 |
ENST00000528099.5 | hg19 | chr11 | 93,474,825 | 93,495,469 | 20,645 |
ENST00000354421.8 | hg19 | chr11 | 93,474,838 | 93,497,915 | 23,078 |
Key | Value |
---|---|
strand | + |
start | 93,474,759 |
Gene Symbol | C11orf54 |
Entrez GeneId | 28,970 |
Chr Band | 11q21 |
end | 93,496,267 |
chr | chr11 |
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