GID4 GID complex subunit 4 homolog
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
not provided | 2 | 0 |
Uncertain significance | 0 | 24 |
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
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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Search word | : | |
Filtering | : |
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 | C17orf39 |
SYNONYM | VID2 |
SYNONYM | VID24 |
MIM | 617699 OMIM |
HGNC | HGNC:28453 HGNC |
Ensembl | ENSG00000141034 Ensembl |
AllianceGenome | HGNC:28453 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000376345.3 | hg38 | chr17 | 18,039,445 | 18,057,467 | 18,023 |
ENST00000268719.9 | hg38 | chr17 | 18,039,408 | 18,068,405 | 28,998 |
ENST00000268719.9 | hg19 | chr17 | 17,942,722 | 17,971,719 | 28,998 |
ENST00000376345.3 | hg19 | chr17 | 17,942,759 | 17,960,781 | 18,023 |
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