Locus NME NAXE

Disease ID
NME
Gene ID
NAXE
Updated
Jun 15, 2026
v2.22.0
Other gene loci
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Disease

Name NAXE-related mitochondrial encephalopathy
Inheritance
Description
Patients with NAXE-related mitochondrial encephalopathy exhibit developmental delay, cognitive regression, altered consciousness, abnormalities in eye movement (including nystagmus), muscle weakness, respiratory failure, seizure, ataxia, and gait disturbance at the age of 1 to 2 years. The disease is characterized by fluctuating symptoms over time, often exacerbated by febrile illness; it is progressive and fatal in the long term .
Prevalence
Single proband found in Japanese cohort .
Age of Onset Age of Onset(Typical)Years1  10  0
Single repeat expansion case had onset at 13 months, while NAXE-related mitochondrial encephalopathy more generally has predominately infantile onset, extending to 20y or older .
HPO Terms
Association
Mendelian

Locus

Details
Benign range (2-7) alleles established by 484 control alleles and validated with orthogonal databases, while single proband had expansion of ~200 repeats inherited from mother via uniparental disomy . While the repeat expansion is newly reported, other variants in the NAXE gene have previously been associated with mitochondrial encephalopathy.
Mechanism
LoF
Reduced NAXE expression from expansion in promoter; hypermethylation was detected at and downstream of the repeat sequence in the proband as well as the maternal copy of the expanded allele, which was not present in the maternal normal range allele nor in the controls
Detection
Year
2024
Location in Gene
5' UTR
Gene Strand

Alleles

Ref. Motif
GGGCC
Ranges BenignIntermediatePathogenicUnits2  70  0200  200
Benign (ref.)
Benign (gene)
Pathogenic (ref.)
GGGCC
Pathogenic (gene)
CCGGG
Unknown (ref.)
Unknown (gene)
Interruption (ref.)
Interruption (gene)

References

Direct supporting references for info on this page.

1
Biallelic GGGCC repeat expansion leading to NAXE-related mitochondrial encephalopathy.
Kokoro,Ozaki, Yukiko,Yatsuka, Yoshinobu,Oyazato, Atsushi,Nishiyama, Kazuhiro R,Nitta, Yoshihito,Kishita, Takuya,Fushimi, Masaru,Shimura, Shohei,Noma, Yohei,Sugiyama, Michihira,Tagami, Moe,Fukunaga, Hiroko,Kinoshita, Tomoko,Hirata, Wataru,Suda, Yasuhiro,Murakawa, Piero,Carninci, Akira,Ohtake, Kei,Murayama, Yasushi,Okazaki
NPJ genomic medicine · 2024-10-25
pmid:39455596

Additional Literature

Additional literature related to this locus.

Raw PubMed search results
(All PubMed results returned by searching for this gene, tandem repeats, and disease, in medline format)

AIBP-LRP2-mediated HDL uptake restricts CXCR4
Lingping,Zhu, Minghong,Chen, Kechuan,Lin, Can,Du, Meilian,Yao, Jing,Chen, Jian,Zhang, Xunjie,Cheng, Dan,Wang, Yu,Liu, Lisha,Liu, Junyu,Chen, Yamei,Liu, Xin,Luo, Guogang,Zhang, Chuanchang,Li, Longhou,Fang, Yongping,Bai
Science advances · 2025-10-15
pmid:41091881