OCEL1 occludin/ELL domain containing 1
Information
- Symbol
- OCEL1
- Type
- protein-coding
- Description
- occludin/ELL domain containing 1
- Entrez Gene ID
- 79629
- Genome
- hg19
- Position
- chr19:17,337,035-17,340,028
- Genome
- hg38
- Position
- chr19:17,226,226-17,229,219
- HGNC
- HGNC:26221 HGNC
- Ensembl
- ENSG00000099330 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 14 |
Likely benign | 0 | 12 |
Uncertain significance | 0 | 38 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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64 |
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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 |
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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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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 | FWP009 |
SYNONYM | S863-9 |
HGNC | HGNC:26221 HGNC |
Ensembl | ENSG00000099330 Ensembl |
AllianceGenome | HGNC:26221 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000597836.5 | hg38 | chr19 | 17,226,615 | 17,229,165 | 2,551 |
ENST00000215061.9 | hg38 | chr19 | 17,226,226 | 17,229,219 | 2,994 |
ENST00000601529.5 | hg38 | chr19 | 17,226,225 | 17,229,215 | 2,991 |
ENST00000601529.5 | hg19 | chr19 | 17,337,034 | 17,340,024 | 2,991 |
ENST00000215061.9 | hg19 | chr19 | 17,337,035 | 17,340,028 | 2,994 |
ENST00000597836.5 | hg19 | chr19 | 17,337,424 | 17,339,974 | 2,551 |
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