Gene
FXYD2
FXYD domain containing ion transport regulator 2
- HGNC 4026↗(opens in a new tab)
- Ensembl gene ENSG00000137731↗(opens in a new tab)
- NCBI Gene 486↗(opens in a new tab)
Summary
- Cytogenetic location
- 11q23.3
- Coordinates
- Chromosome 11: 117,820,057–117,824,744 (GRCh38)
- Exons
- 6 exons across 4.7 kb
- Protein
- 66 amino acids
- Also known as
- MGC12372
- Previous symbols
- ATP1G1, HOMG2
- MANE Select transcript
- ENST00000292079.7NM_001680.5
- 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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Familial Hypomagnesemia
- Familial Primary Hypomagnesemia
A group of inherited magnesium-wasting disorders caused by variants in genes such as CLDN16, CLDN19, TRPM6, CNNM2 and FXYD2; the CLDN16 and CLDN19 forms can progress to chronic kidney disease.
- ClinGen rates the link moderate
- 1 GenCC submitter rates it definitive or strong
What knowing changes
Magnesium supplementation can control symptoms, and some forms need kidney function and eye monitoring.
How FXYD2 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
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 0.6 kb of the gene's 4.7 kb; 201 of those bases code for the protein.
Genes linked to the same conditions
- ATP1A1ATPase Na+/K+ transporting subunit alpha 1Shares 1 condition
- CLDN16claudin 16Shares 1 condition
- CLDN19claudin 19Shares 1 condition
- CNNM2cyclin and CBS domain divalent metal cation transport mediator 2Shares 1 condition
- RRAGDRas related GTP binding DShares 1 condition
- TRPM6transient receptor potential cation channel subfamily M member 6Shares 1 condition
- TRPM7transient receptor potential cation channel subfamily M member 7Shares 1 condition
- TRPV6transient receptor potential cation channel subfamily V member 6Shares 1 condition
Traits linked to FXYD2
The Human Phenotype Ontology lists these as features of the rare conditions FXYD2 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.
- 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.). FXYD2 gene: FXYD domain containing ion transport regulator 2. Retrieved 17 October 2026, from https://dantelabs.com/genes/fxyd2
Dante Labs. FXYD2 gene: FXYD domain containing ion transport regulator 2 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/fxyd2
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