C18orf54 chromosome 18 open reading frame 54
Information
- Symbol
- C18orf54
- Type
- protein-coding
- Description
- chromosome 18 open reading frame 54
- Entrez Gene ID
- 162681
- Genome
- hg19
- Position
- chr18:51,884,276-51,908,404
- Genome
- hg38
- Position
- chr18:54,357,906-54,382,034
- MIM
- 613258 OMIM
- HGNC
- HGNC:13796 HGNC
- Ensembl
- ENSG00000166845 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
2 |
 |
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 | LAS2 |
| MIM | 613258 OMIM |
| HGNC | HGNC:13796 HGNC |
| Ensembl | ENSG00000166845 Ensembl |
| AllianceGenome | HGNC:13796 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000648616.1 | hg38 | chr18 | 54,358,482 | 54,378,845 | 20,364 |
| ENST00000578138.5 | hg38 | chr18 | 54,357,917 | 54,378,434 | 20,518 |
| ENST00000620105.5 | hg38 | chr18 | 54,357,906 | 54,382,034 | 24,129 |
| ENST00000382911.8 | hg38 | chr18 | 54,358,585 | 54,380,368 | 21,784 |
| ENST00000300091.5 | hg38 | chr18 | 54,358,585 | 54,382,032 | 23,448 |
| ENST00000620105.5 | hg19 | chr18 | 51,884,276 | 51,908,404 | 24,129 |
| ENST00000578138.5 | hg19 | chr18 | 51,884,287 | 51,904,804 | 20,518 |
| ENST00000648616.1 | hg19 | chr18 | 51,884,852 | 51,905,215 | 20,364 |
| ENST00000382911.8 | hg19 | chr18 | 51,884,955 | 51,906,738 | 21,784 |
| ENST00000300091.5 | hg19 | chr18 | 51,884,955 | 51,908,402 | 23,448 |
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