DGCR11 DiGeorge syndrome critical region gene 11
Information
- Symbol
- DGCR11
- Type
- ncRNA
- Description
- DiGeorge syndrome critical region gene 11
- Entrez Gene ID
- 25786
- Genome
- hg19
- Position
- chr22:19,033,675-19,035,888
- Genome
- hg38
- Position
- chr22:19,046,162-19,048,375
- HGNC
- HGNC:17226 HGNC
- Ensembl
- ENSG00000273311 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 14 | 0 |
Ranking
ClinVar | |
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Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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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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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ENST00000609958.1 | hg38 | chr22 | 19,046,162 | 19,048,375 | 2,214 |
ENST00000609958.1 | hg19 | chr22 | 19,033,675 | 19,035,888 | 2,214 |
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