Gene
HJV
hemojuvelin BMP co-receptor
- HGNC 4887↗(opens in a new tab)
- Ensembl gene ENSG00000168509↗(opens in a new tab)
- NCBI Gene 148738↗(opens in a new tab)
Summary
- Cytogenetic location
- 1q21.1
- Coordinates
- Chromosome 1: 146,017,470–146,021,735 (GRCh38)
- Exons
- 4 exons across 4.3 kb
- Protein
- 426 amino acids
- Also known as
- JH, HFE2A, RGMC, hemojuvelin, haemojuvelin
- Previous symbols
- HFE2
- MANE Select transcript
- ENST00000336751.11NM_213653.4
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Hemochromatosis
- Hereditary Hemochromatosis
An inherited metabolic disorder characterized by iron accumulation in the tissues.
- ClinGen rates the link definitive
- 6 GenCC submitters rate it definitive or strong
What knowing changes
Phlebotomy, iron chelation, iron restriction diet, family screening
How HJV is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
Exons make up 2.1 kb of the gene's 4.3 kb; 1,281 of those bases code for the protein.
How a genome test reads HJV
48
positions in HJV where ClinVar classes a change as pathogenic or likely pathogenic
None of them falls in a region short reads find hard.
A whole genome covers all 4.3 kb of HJV, introns included, not only the 2.1 kb of exons.
Genes linked to the same conditions
Traits linked to HJV
The Human Phenotype Ontology lists these as features of the rare conditions HJV can cause. Each trait's page lists the other genes linked to it.
External links
Gene records
Transcript
Protein
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
- GenCC and ClinGen, released 2026-10-16: which conditions the gene is linked to, and how strongly.
- The ACMG secondary findings list, SF v3.2.
- ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). HJV gene: hemojuvelin BMP co-receptor. Retrieved 16 October 2026, from https://dantelabs.com/genes/hjv
Dante Labs. HJV gene: hemojuvelin BMP co-receptor [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/hjv
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