GDF15 growth differentiation factor 15
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 8 |
Likely benign | 0 | 4 |
risk factor | 0 | 2 |
Uncertain significance | 0 | 52 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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64 |
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2 |
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 |
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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 |
Search Word
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 | GDF-15 |
SYNONYM | HG |
SYNONYM | MIC-1 |
SYNONYM | MIC1 |
SYNONYM | NAG-1 |
SYNONYM | |
SYNONYM | PLAB |
SYNONYM | PTGFB |
MIM | 605312 OMIM |
HGNC | HGNC:30142 HGNC |
Ensembl | ENSG00000130513 Ensembl |
AllianceGenome | HGNC:30142 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000595973.3 | hg38 | chr19 | 18,382,170 | 18,388,935 | 6,766 |
ENST00000252809.3 | hg38 | chr19 | 18,386,158 | 18,389,176 | 3,019 |
ENST00000597765.2 | hg38 | chr19 | 18,374,731 | 18,388,935 | 14,205 |
ENST00000597765.2 | hg19 | chr19 | 18,485,541 | 18,499,745 | 14,205 |
ENST00000595973.3 | hg19 | chr19 | 18,492,980 | 18,499,745 | 6,766 |
ENST00000252809.3 | hg19 | chr19 | 18,496,968 | 18,499,986 | 3,019 |
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