HMOX1 heme oxygenase 1
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 2 | 30 |
| Likely pathogenic | 0 | 10 |
| Benign | 0 | 24 |
| Likely benign | 0 | 302 |
| Conflicting classifications of pathogenicity | 0 | 6 |
| Uncertain significance | 0 | 166 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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38 |
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484 |
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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
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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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | HMOX1D |
| SYNONYM | HO-1 |
| SYNONYM | HSP32 |
| SYNONYM | bK286B10 |
| MIM | 141250 OMIM |
| HGNC | HGNC:5013 HGNC |
| Ensembl | ENSG00000100292 Ensembl |
| AllianceGenome | HGNC:5013 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000216117.9 | hg38 | chr22 | 35,381,096 | 35,394,207 | 13,112 |
| ENST00000679074.1 | hg38 | chr22 | 35,381,096 | 35,394,207 | 13,112 |
| ENST00000677931.1 | hg38 | chr22 | 35,381,096 | 35,394,207 | 13,112 |
| ENST00000216117.9 | hg19 | chr22 | 35,777,089 | 35,790,200 | 13,112 |
| ENST00000677931.1 | hg19 | chr22 | 35,777,089 | 35,790,200 | 13,112 |
| ENST00000679074.1 | hg19 | chr22 | 35,777,089 | 35,790,200 | 13,112 |
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