IGF2 insulin like growth factor 2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 2 | 28 |
Likely pathogenic | 0 | 20 |
Benign | 0 | 14 |
Likely benign | 0 | 68 |
Conflicting classifications of pathogenicity | 0 | 8 |
not provided | 8 | 0 |
Uncertain significance | 0 | 136 |
Ranking
ClinVar | |
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0 |
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0 |
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30 |
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220 |
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12 |
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
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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 |
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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 |
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Target data | : |
MGeND data only
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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 | C11orf43 |
SYNONYM | GRDF |
SYNONYM | IGF-II |
SYNONYM | PP9974 |
SYNONYM | SRS3 |
MIM | 147470 OMIM |
HGNC | HGNC:5466 HGNC |
Ensembl | ENSG00000167244 Ensembl |
AllianceGenome | HGNC:5466 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000381389.5 | hg38 | chr11 | 2,132,673 | 2,141,016 | 8,344 |
ENST00000381395.5 | hg38 | chr11 | 2,129,112 | 2,137,290 | 8,179 |
ENST00000381392.5 | hg38 | chr11 | 2,132,640 | 2,137,287 | 4,648 |
ENST00000434045.6 | hg38 | chr11 | 2,132,500 | 2,141,238 | 8,739 |
ENST00000416167.7 | hg38 | chr11 | 2,129,117 | 2,139,389 | 10,273 |
ENST00000481781.3 | hg38 | chr11 | 2,132,500 | 2,158,391 | 25,892 |
ENST00000381406.8 | hg38 | chr11 | 2,129,112 | 2,138,974 | 9,863 |
ENST00000418738.2 | hg38 | chr11 | 2,132,716 | 2,137,305 | 4,590 |
ENST00000695541.1 | hg38 | chr11 | 2,131,395 | 2,149,579 | 18,185 |
ENST00000381395.5 | hg19 | chr11 | 2,150,342 | 2,158,520 | 8,179 |
ENST00000381406.8 | hg19 | chr11 | 2,150,342 | 2,160,204 | 9,863 |
ENST00000416167.7 | hg19 | chr11 | 2,150,347 | 2,160,619 | 10,273 |
ENST00000695541.1 | hg19 | chr11 | 2,152,625 | 2,170,809 | 18,185 |
ENST00000434045.6 | hg19 | chr11 | 2,153,730 | 2,162,468 | 8,739 |
ENST00000481781.3 | hg19 | chr11 | 2,153,730 | 2,179,621 | 25,892 |
ENST00000381392.5 | hg19 | chr11 | 2,153,870 | 2,158,517 | 4,648 |
ENST00000381389.5 | hg19 | chr11 | 2,153,903 | 2,162,246 | 8,344 |
ENST00000418738.2 | hg19 | chr11 | 2,153,946 | 2,158,535 | 4,590 |
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