GAN

gigaxonin

Relationship to CMT

GAN AR 1 subtype 16q23.2
First described 2000
Subtype1
SubtypeInheritanceClassOMIMSentinel Publication
SubtypeGAN-1 Inheritanceautosomal recessive ClassGAN OMIM256850 Sentinel Publication
2000 · 10.1038/81701

ClinVar Variants

Pathogenic and likely pathogenic variants in GAN, as classified in ClinVar, are read live from NCBI.

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.

What the review stars mean

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, and one for a single submitter with criteria provided. A record with no criteria provided earns no stars and is not indexed.

Only aggregate germline records are indexed. 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.

Gene Function

GAN probable cytoskeletal component that directly or indirectly plays an important role in neurofilament architecture. May act as a substrate-specific adapter of an E3 ubiquitin-protein ligase complex which mediates the ubiquitination and subsequent proteasomal degradation of target proteins. Controls degradation of TBCB. Controls degradation of MAP1B and MAP1S, and is critical for neuronal maintenance and survival Source: UniProt

Indexed Identifiers

HGNC Aliases: GAN1
hgnc_idHGNC:4137
ensembl_gene_idENSG00000261609
coords_grch38chr16:81314932-81390884
coords_grch37chr16:81348557-81424489
entrez_id8139
omim_gene605379
uniprot_idsQ9H2C0
refseq_accessionNM_001377486
mane_refseqNM_022041.4
mane_ensemblENST00000648994.2

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