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Molecular autopsy

Gene: HAL

Red List (low evidence)
HAL (histidine ammonia-lyase)
EnsemblGeneIds (GRCh38): ENSG00000084110
EnsemblGeneIds (GRCh37): ENSG00000084110
OMIM: 609457, Gene2Phenotype
HAL is in 3 panels

0 reviews

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
Phenotypes
  • Histidinaemia (Disorders of histidine, tryptophan or lysine metabolism)
OMIM
609457
Clinvar variants
Variants in HAL
Penetrance
None
Publications
Panels with this gene

History Filter Activity

20 Dec 2018, Gel status: 1

Set Phenotypes

Ellen McDonagh (Genomics England Curator)

Added phenotypes Histidinaemia (Disorders of histidine, tryptophan or lysine metabolism) for gene: HAL

20 Dec 2018, Gel status: 1

Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes

Ellen McDonagh (Genomics England Curator)

gene: HAL was added gene: HAL was added to Molecular autopsy. Sources: Expert Review Red Mode of inheritance for gene: HAL was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: HAL were set to 27604308 Phenotypes for gene: HAL were set to Histidinaemia (Disorders of histidine, tryptophan or lysine metabolism)