NAGLU

N-acetyl-alpha-glucosaminidase

Gene Function

Involved in the degradation of heparan sulfate Source: UniProt

Relationship to CMT

CMT2 AD
1 subtype
17q21.2
First described 2015

Subtype Inheritance Class OMIM Sentinel Publication
SubtypeCMT2V Inheritanceautosomal dominant ClassCMT2 OMIM616491 Sentinel Publication

2015 · 10.1093/brain/awv074

Stored Identifiers

HGNC Aliases: NAG
hgnc_idHGNC:7632
ensembl_gene_idENSG00000108784
coords_grch38chr17:42536216-42544449
coords_grch37chr17:40688190-40696467
entrez_id4669
omim_gene609701
uniprot_idsP54802
refseq_accessionNM_000263
mane_refseqNM_000263.4
mane_ensemblENST00000225927.7

ClinVar Variants

Pathogenic and likely pathogenic variants in NAGLU, as classified in ClinVar, are read live from NCBI. Only aggregate germline records are shown. Uncertain and conflicting classifications are not. Experts in CMT makes no claim to the accuracy of ClinVar data. This index is provided for informational purposes only.

Review stars are ClinVar’s measure of how well a classification is supported: four for a practice guideline, three for an expert panel review, two for agreement among multiple submitters, one for a single submitter with criteria provided, and none where no criteria were provided.

Reported in CMT
Reported in Other Diseases

Reported in a disease other than CMT. Listed apart rather than counted as CMT variants.

Variants w/o a Recorded Disease

Pathogenic or likely pathogenic in ClinVar, submitted without a disease recorded.

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