ELF4 E74 like ETS transcription factor 4
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 8 |
Benign | 0 | 8 |
Likely benign | 0 | 12 |
not provided | 6 | 0 |
Uncertain significance | 0 | 44 |
Ranking
ClinVar | |
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0 |
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0 |
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4 |
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56 |
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10 |
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 | : | |
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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 | AIFBL2 |
SYNONYM | ELFR |
SYNONYM | MEF |
MIM | 300775 OMIM |
HGNC | HGNC:3319 HGNC |
Ensembl | ENSG00000102034 Ensembl |
AllianceGenome | HGNC:3319 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000335997.11 | hg38 | chrX | 130,064,874 | 130,110,716 | 45,843 |
ENST00000308167.10 | hg38 | chrX | 130,063,955 | 130,110,497 | 46,543 |
ENST00000308167.10 | hg19 | chrX | 129,197,930 | 129,244,472 | 46,543 |
ENST00000335997.11 | hg19 | chrX | 129,198,849 | 129,244,691 | 45,843 |
Key | Value |
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strand | - |
UniProt | OG |
start | 129,198,894 |
Gene Symbol | ELF4 |
Entrez GeneId | 2,000 |
Chr Band | Xq26 |
end | 129,244,687 |
chr | chrX |
Name | E74-like factor 4 (ets domain transcription factor) |
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