ANGPTL4 angiopoietin like 4
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 18 |
Likely benign | 0 | 14 |
association | 0 | 4 |
Uncertain significance | 0 | 38 |
Ranking
ClinVar | |
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0 |
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0 |
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2 |
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68 |
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4 |
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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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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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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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 | ARP4 |
SYNONYM | FIAF |
SYNONYM | HARP |
SYNONYM | HFARP |
SYNONYM | NL2 |
SYNONYM | PGAR |
SYNONYM | TGQTL |
SYNONYM | UNQ171 |
SYNONYM | pp1158 |
MIM | 605910 OMIM |
HGNC | HGNC:16039 HGNC |
Ensembl | ENSG00000167772 Ensembl |
AllianceGenome | HGNC:16039 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000393962.6 | hg38 | chr19 | 8,364,169 | 8,374,331 | 10,163 |
ENST00000301455.7 | hg38 | chr19 | 8,364,155 | 8,374,370 | 10,216 |
ENST00000301455.7 | hg19 | chr19 | 8,429,039 | 8,439,254 | 10,216 |
ENST00000393962.6 | hg19 | chr19 | 8,429,053 | 8,439,215 | 10,163 |
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