DENND11 DENN domain containing 11
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 70 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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70 |
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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 |
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 |
Type | ID |
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SYNONYM | KIAA1147 |
SYNONYM | LCHN |
SYNONYM | PRO2561 |
MIM | 620122 OMIM |
HGNC | HGNC:29472 HGNC |
Ensembl | ENSG00000257093 Ensembl |
AllianceGenome | HGNC:29472 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000482493.1 | hg38 | chr7 | 141,661,930 | 141,701,615 | 39,686 |
ENST00000536163.6 | hg38 | chr7 | 141,656,728 | 141,702,166 | 45,439 |
ENST00000536163.6 | hg19 | chr7 | 141,356,528 | 141,401,966 | 45,439 |
ENST00000482493.1 | hg19 | chr7 | 141,361,730 | 141,401,415 | 39,686 |
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