Gene
AUH
AU RNA binding methylglutaconyl-CoA hydratase
- HGNC 890↗(opens in a new tab)
- Ensembl gene ENSG00000148090↗(opens in a new tab)
- NCBI Gene 549↗(opens in a new tab)
Summary
- Cytogenetic location
- 9q22.31
- Coordinates
- Chromosome 9: 91,213,823–91,361,918 (GRCh38)
- Exons
- 10 exons across 148.1 kb
- Protein
- 339 amino acids
- MANE Select transcript
- ENST00000375731.9NM_001698.3
- 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.
Read AUH, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome TestCurated reports relevant to this gene
No Genome Test report reads AUH yet. The test sequences your whole genome, so your data includes it all the same.
How AUH is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
- Stretches short reads find hard
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 1.6 kb of the gene's 148.1 kb; 1,020 of those bases code for the protein.
How a genome test reads AUH
22
positions in AUH 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 148.1 kb of AUH, introns included, not only the 1.6 kb of exons.
Traits linked to AUH
The Human Phenotype Ontology lists these as features of the rare conditions AUH can cause. Each trait's page lists the other genes linked to it.
Abnormality of the nervous system
- Abnormal cerebral white matter morphology
- Ataxia
- Delayed speech and language development
- Global developmental delay
- Abnormal basal ganglia morphology
- Coma
- Dementia
- Dystonia
Show 12 more traits
- Epilepsy
- Involuntary writhing movements in fingers, hands, toes, and feet
- Progressive cerebellar ataxia
- Self-mutilation
- Cognitive impairment
- Degeneration of cerebrum
- Difficulty articulating speech
- Febrile seizure (within the age range of 3 months to 6 years)
- Increased reflexes
- Leukoencephalopathy
- Motor delay
- Short attention span
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.
- 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.). AUH gene: AU RNA binding methylglutaconyl-CoA hydratase. Retrieved 17 October 2026, from https://dantelabs.com/genes/auh
Dante Labs. AUH gene: AU RNA binding methylglutaconyl-CoA hydratase [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/auh
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks