UNC119B unc-119 lipid binding chaperone B
Information
- Symbol
- UNC119B
- Type
- protein-coding
- Description
- unc-119 lipid binding chaperone B
- Entrez Gene ID
- 84747
- Genome
- hg19
- Position
- chr12:121,148,261-121,161,443
- Genome
- hg38
- Position
- chr12:120,710,458-120,723,640
- MIM
- 620513 OMIM
- HGNC
- HGNC:16488 HGNC
- Ensembl
- ENSG00000175970 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 28 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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28 |
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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
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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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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 |
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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 |
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SYNONYM | POC7B |
MIM | 620513 OMIM |
HGNC | HGNC:16488 HGNC |
Ensembl | ENSG00000175970 Ensembl |
AllianceGenome | HGNC:16488 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000344651.5 | hg38 | chr12 | 120,710,458 | 120,723,640 | 13,183 |
ENST00000344651.5 | hg19 | chr12 | 121,148,261 | 121,161,443 | 13,183 |
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