HJV hemojuvelin BMP co-receptor
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 94 |
Likely pathogenic | 0 | 28 |
Benign | 0 | 14 |
Likely benign | 0 | 406 |
Conflicting classifications of pathogenicity | 0 | 28 |
not provided | 5 | 0 |
Uncertain significance | 0 | 174 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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44 |
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660 |
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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
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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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 |
---|---|
SYNONYM | HFE2 |
SYNONYM | HFE2A |
SYNONYM | JH |
SYNONYM | RGMC |
MIM | 608374 OMIM |
HGNC | HGNC:4887 HGNC |
Ensembl | ENSG00000168509 Ensembl |
AllianceGenome | HGNC:4887 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000497365.5 | hg38 | chr1 | 146,017,468 | 146,021,735 | 4,268 |
ENST00000634927.1 | hg38 | chr1 | 146,018,567 | 146,021,735 | 3,169 |
ENST00000636675.1 | hg38 | chr1 | 146,017,547 | 146,036,746 | 19,200 |
ENST00000336751.11 | hg38 | chr1 | 146,017,470 | 146,021,735 | 4,266 |
ENST00000357836.5 | hg38 | chr1 | 146,017,470 | 146,021,918 | 4,449 |
ENST00000475797.1 | hg38 | chr1 | 146,017,468 | 146,021,734 | 4,267 |
ENST00000336751.11 | hg19 | chr1 | 145,413,278 | 145,417,543 | 4,266 |
ENST00000357836.5 | hg19 | chr1 | 145,413,095 | 145,417,543 | 4,449 |
ENST00000475797.1 | hg19 | chr1 | 145,413,279 | 145,417,545 | 4,267 |
ENST00000497365.5 | hg19 | chr1 | 145,413,278 | 145,417,545 | 4,268 |
ENST00000636675.1 | hg19 | chr1 | 145,398,250 | 145,417,466 | 19,217 |
ENST00000634927.1 | hg19 | chr1 | 145,413,278 | 145,416,446 | 3,169 |
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