Also known as HIS, HSTD, histidine ammonia-lyase, Histidine ammonia-lyase
protein-coding gene in the species Homo sapiens
Gene data
HAL- Name
- histidine ammonia-lyase
- Type
- protein-coding
- Aliases
- HIS, HSTD
Histidine ammonia-lyase is a cytosolic enzyme catalyzing the first reaction in histidine catabolism, the nonoxidative deamination of L-histidine to trans-urocanic acid. Histidine ammonia-lyase defects cause histidinemia which is characterized by increased histidine and histamine and decreased urocanic acid in body fluids. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012].
via MyGene.info
Gene · Ensembl
histidine ammonia-lyase
- Symbol
- HAL
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 12:95,972,662-95,996,365
- Strand
- Reverse (−)
- Assembly
- GRCh38
View on Ensembl →
via Ensembl · EMBL-EBI
Wikidata facts
Show 6 more facts
- HomoloGene ID
- 68229
- exact match
- identifiers.org/ncbigene/3034
- genomic end
- 96390143
- genomic start
- 96366440
- cytogenetic location
- 12q23.1
- Commons category
- Histidine ammonia-lyase (HAL)
Sources (4)
via Wikidata · CC0
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