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Newborns main panel

Gene: NAXD

Amber List (moderate evidence)

NAXD (NAD(P)HX dehydratase)
EnsemblGeneIds (GRCh38): ENSG00000213995
EnsemblGeneIds (GRCh37): ENSG00000213995
OMIM: 615910, Gene2Phenotype
NAXD is in 6 panels

1 review

Mafalda Gomes (Genomics England Curator)

The mechanism of pathogenicity is loss-of-function (LOF).
Created: 1 Jun 2023, 2:40 p.m. | Last Modified: 1 Jun 2023, 2:40 p.m.
Panel Version: 0.137
PMID: 30576410 - 6 cases PMID: 32462209 - 1 case PMID: 31755961 - 1 case PMID: 35231119 - 1 case PMID: 36158054 - 1 case PMID: 36834994 - 1 case
Created: 1 Jun 2023, 12:22 p.m. | Last Modified: 1 Jun 2023, 12:22 p.m.
Panel Version: 0.134

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
Phenotypes
  • early-onset progressive encephalopathy with brain edema and/or leukoencephalopathy 2
OMIM
615910
Clinvar variants
Variants in NAXD
Penetrance
None
Panels with this gene

History Filter Activity

14 Sep 2023, Gel status: 2

Added New Source, Set Phenotypes, Status Update

Mafalda Gomes (Genomics England Curator)

Source Expert Review Amber was added to NAXD. Added phenotypes early-onset progressive encephalopathy with brain edema and/or leukoencephalopathy 2 for gene: NAXD Rating Changed from Green List (high evidence) to Amber List (moderate evidence)

5 Jul 2023, Gel status: 3

Added New Source, Set Phenotypes, Status Update

Mafalda Gomes (Genomics England Curator)

Source Expert Review Green was added to NAXD. Added phenotypes early-onset progressive encephalopathy with brain edema and/or leukoencephalopathy 2 for gene: NAXD Rating Changed from Amber List (moderate evidence) to Green List (high evidence)

31 May 2023, Gel status: 2

Added New Source, Set Phenotypes, Status Update

Mafalda Gomes (Genomics England Curator)

Source Expert Review Amber was added to NAXD. Added phenotypes early-onset progressive encephalopathy with brain edema and/or leukoencephalopathy 2 for gene: NAXD Rating Changed from Green List (high evidence) to Amber List (moderate evidence)

5 May 2023, Gel status: 3

Added New Source, Set Phenotypes, Status Update

Mafalda Gomes (Genomics England Curator)

Source Expert Review Green was added to NAXD. Added phenotypes early-onset progressive encephalopathy with brain edema and/or leukoencephalopathy 2 for gene: NAXD Rating Changed from No List (delete) to Green List (high evidence)

27 Mar 2023, Gel status: 0

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

Mafalda Gomes (Genomics England Curator)

gene: NAXD was added gene: NAXD was added to Newborns main panel. Sources: Expert Review Removed Mode of inheritance for gene: NAXD was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: NAXD were set to early-onset progressive encephalopathy with brain edema and/or leukoencephalopathy 2