IL4 interleukin 4
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Uncertain significance | 0 | 16 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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18 |
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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
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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 |
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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 | BCGF-1 |
SYNONYM | BCGF1 |
SYNONYM | BSF-1 |
SYNONYM | BSF1 |
SYNONYM | IL-4 |
MIM | 147780 OMIM |
HGNC | HGNC:6014 HGNC |
Ensembl | ENSG00000113520 Ensembl |
AllianceGenome | HGNC:6014 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000231449.7 | hg38 | chr5 | 132,673,989 | 132,682,678 | 8,690 |
ENST00000622422.1 | hg38 | chr5 | 132,673,986 | 132,682,676 | 8,691 |
ENST00000350025.2 | hg38 | chr5 | 132,674,051 | 132,682,587 | 8,537 |
ENST00000622422.1 | hg19 | chr5 | 132,009,678 | 132,018,368 | 8,691 |
ENST00000231449.7 | hg19 | chr5 | 132,009,681 | 132,018,370 | 8,690 |
ENST00000350025.2 | hg19 | chr5 | 132,009,743 | 132,018,279 | 8,537 |
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