ELK3 ETS transcription factor ELK3
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 42 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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52 |
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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 |
---|---|
SYNONYM | ERP |
SYNONYM | NET |
SYNONYM | SAP-2 |
SYNONYM | SAP2 |
MIM | 600247 OMIM |
HGNC | HGNC:3325 HGNC |
Ensembl | ENSG00000111145 Ensembl |
AllianceGenome | HGNC:3325 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000552142.5 | hg38 | chr12 | 96,194,545 | 96,267,830 | 73,286 |
ENST00000228741.8 | hg38 | chr12 | 96,194,375 | 96,269,824 | 75,450 |
ENST00000228741.8 | hg19 | chr12 | 96,588,153 | 96,663,602 | 75,450 |
ENST00000552142.5 | hg19 | chr12 | 96,588,323 | 96,661,608 | 73,286 |
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