01
2-methyl-3-hydroxybutyric aciduria
2-methyl-3-hydroxybutyric aciduria
2-methyl-3-hydroxybutyric aciduria
- Entity Type
- Targets
- Relation Groups
- 5
- Relation Preview
- 37
Basic Information
Grouped by core information, identifiers, and descriptions.
Core Information
- Gene Symbol
- AUH
- Protein Name
- AU RNA binding methylglutaconyl-CoA hydratase
- Gene Type
- protein-coding
- Chromosome
- 9
- Map Location
- 9q22.31
Identifiers
- Entrez ID
- 549
- Ensembl ID
- ENSG00000148090
- UniProt ID
- No data
- HGNC ID
- No data
- PDB ID
- No data
Description and Extensions
- Description
- No data
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Related Diseases
target disease8 Diseases
02
3-@METHYLGLUTACONIC ACIDURIA, TYPE I
3-@methylglutaconic aciduria, type i
3-@methylglutaconic aciduria, type i
03
3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency
3-hydroxy-3-methylglutaryl-coa synthase 2 deficiency
3-hydroxy-3-methylglutaryl-coa synthase 2 deficiency
04
05
3-Methylglutaconic aciduria type 1
3-methylglutaconic aciduria type 1
3-methylglutaconic aciduria type 1
06
3-Methylglutaconic Aciduria Type 3
3-methylglutaconic aciduria type 3
3-methylglutaconic aciduria type 3
07
3-Methylglutaconic Aciduria Type Iv With Sensorineural Deafness, Encephalopathy And Leigh-Like Syndrome
3-methylglutaconic aciduria type iv with sensorineural deafness, encephalopathy and leigh-like syndrome
3-methylglutaconic aciduria type iv with sensorineural deafness, encephalopathy and leigh-like syndrome
08
3-Methylglutaconic Aciduria With Deafness, Encephalopathy, And Leigh-Like Syndrome
3-methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome
3-methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome