UBQLNL ubiquilin like
Information
- Symbol
- UBQLNL
- Type
- protein-coding
- Description
- ubiquilin like
- Entrez Gene ID
- 143630
- Genome
- hg19
- Position
- chr11:5,535,623-5,537,929
- Genome
- hg38
- Position
- chr11:5,514,393-5,516,699
- HGNC
- HGNC:28294 HGNC
- Ensembl
- ENSG00000175518 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 8 |
Uncertain significance | 0 | 52 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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66 |
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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 |
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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000673910.1 | hg38 | chr11 | 5,514,393 | 5,518,431 | 4,039 |
ENST00000380184.2 | hg38 | chr11 | 5,514,393 | 5,516,699 | 2,307 |
ENST00000380184.2 | hg19 | chr11 | 5,535,623 | 5,537,929 | 2,307 |
ENST00000673910.1 | hg19 | chr11 | 5,535,623 | 5,539,661 | 4,039 |
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