Genomic Map
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Target Gene Details
Entrez Gene ID: | 3162 |
Gene Name: | heme oxygenase 1 |
Gene Aliases: |
HMOX1D, HO-1, HSP32, bK286B10 |
Location: |
Chr.22:35381067-35394214 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| HMOX1 | NM_002133.2 | NP_002124.1 | ||
| AF051791.1 | ||||
| AK313120.1 | ||||
| BC001491.2 | AAH01491.1 | |||
| BP288767.1 | ||||
| BT019785.1 | AAV38588.1 | |||
| CR456505.1 | CAG30391.1 | |||
| CR541945.1 | CAG46743.1 | |||
| CR541968.1 | CAG46766.1 | |||
| JF323038.1 | ||||
| M23041.1 | AAA50403.1 | |||
| X06985.1 | CAA30045.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv3611 | Chr.22:35363383 - 35385153 on Build GRCh38 | Insertion |
 HMOX1
|
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Additional Information:
For this assay, SNP(s) [rs116814805] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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