Locus OPML1 NUTM2B-AS1
Disease ID
OPML1
Gene ID
NUTM2B-AS1
Updated
Aug 24, 2026
v2.26.0
v2.26.0
Other gene loci
–
Clinical Links
Bioinformatical Links
Disease
–
Name Oculopharyngeal myopathy with leukoencephalopathy 1
Inheritance
Description
Prevalence Rare, found in individuals of East Asian ancestry1 .
Age of Onset 15-40 (only characterized in one family)3 .
HPO Terms
HP:0000508 PtosisHP:0000544 External ophthalmoplegiaHP:0001251 AtaxiaHP:0001260 DysarthriaHP:0001337 TremorHP:0002015 DysphagiaHP:0002059 Cerebral atrophyHP:0002460 Distal muscle weaknessHP:0002579 Gastrointestinal dysmotilityHP:0002878 Respiratory failureHP:0003701 Proximal muscle weaknessHP:0030319 Weakness of facial musculature
Association
Mendelian
Locus
Details
Detection
Year Year first published 20193
Location in Gene
Exon 1 of lncRNA (noncoding)
Gene Strand
Alleles
Ref. Motif Reference motif, reference orientation
CGG
Ranges
Benign (ref.) Benign motif, reference orientation
–
Benign (gene) Benign motif, gene orientation
–
Pathogenic (ref.) Pathogenic motif, reference orientation
CGG
Pathogen. (gene) Pathogenic motif, gene orientation
CGG
Unknown (ref.) Unknown motif, reference orientation
–
Unknown (gene) Unknown motif, gene orientation
–
Interruption (ref.) Interruption motif, reference orientation
–
Interrup. (gene) Interruption motif, gene orientation
–
gnomAD
References
Direct supporting references for info on this page.
1
Neurological disorders caused by novel non-coding repeat expansions: clinical features and differential diagnosis.
Elisa,Vegezzi, Hiroyuki,Ishiura, D Cristopher,Bragg, David,Pellerin, Francesca,Magrinelli, Riccardo,Currò, Stefano,Facchini, Arianna,Tucci, John,Hardy, Nutan,Sharma, Matt C,Danzi, Stephan,Zuchner, Bernard,Brais, Mary M,Reilly, Shoji,Tsuji, Henry,Houlden, Andrea,Cortese
The Lancet. Neurology · 2024-07-01
pmid:388767502
Repeat expansion disorders.
Zhongbo,Chen, Huw R,Morris, James,Polke, Nicholas W,Wood, Sonia,Gandhi, Mina,Ryten, Henry,Houlden, Arianna,Tucci
Practical neurology · 2025-05-15
pmid:393490433
Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease.
Hiroyuki,Ishiura, Shota,Shibata, Jun,Yoshimura, Yuta,Suzuki, Wei,Qu, Koichiro,Doi, M Asem,Almansour, Junko Kanda,Kikuchi, Makiko,Taira, Jun,Mitsui, Yuji,Takahashi, Yaeko,Ichikawa, Tatsuo,Mano, Atsushi,Iwata, Yasuo,Harigaya, Miho Kawabe,Matsukawa, Takashi,Matsukawa, Masaki,Tanaka, Yuichiro,Shirota, Ryo,Ohtomo, Hisatomo,Kowa, Hidetoshi,Date, Aki,Mitsue, Hiroyuki,Hatsuta, Satoru,Morimoto, Shigeo,Murayama, Yasushi,Shiio, Yuko,Saito, Akihiko,Mitsutake, Mizuho,Kawai, Takuya,Sasaki, Yusuke,Sugiyama, Masashi,Hamada, Gaku,Ohtomo, Yasuo,Terao, Yoshihiko,Nakazato, Akitoshi,Takeda, Yoshio,Sakiyama, Yumi,Umeda-Kameyama, Jun,Shinmi, Katsuhisa,Ogata, Yutaka,Kohno, Shen-Yang,Lim, Ai Huey,Tan, Jun,Shimizu, Jun,Goto, Ichizo,Nishino, Tatsushi,Toda, Shinichi,Morishita, Shoji,Tsuji
Nature genetics · 2019-07-22
pmid:313323804
CGG repeat expansion in LOC642361/NUTM2B-AS1 typically presents as oculopharyngodistal myopathy.
Yan,Shi, Chunyan,Cao, Yiheng,Zeng, Yuanliang,Ding, Long,Chen, Fuze,Zheng, Xuejiao,Chen, Fanggui,Zhou, Xiefeng,Yang, Jinjing,Li, Liuqing,Xu, Guorong,Xu, Minting,Lin, Hiroyuki,Ishiura, Shoji,Tsuji, Ning,Wang, Zhiqiang,Wang, Wan-Jin,Chen, Kang,Yang
Journal of genetics and genomics = Yi chuan xue bao · 2023-12-29
pmid:381598795
Non-coding CGG repeat expansion in
Xinyu,Gu, Jiaxi,Yu, Kexin,Jiao, Jianwen,Deng, Xingyu,Xia, Kai,Qiao, Dongyue,Yue, Mingshi,Gao, Chongbo,Zhao, Jihong,Dong, Gongchun,Huang, Jingli,Shan, Chuanzhu,Yan, Li,Di, Yuwei,Da, Wenhua,Zhu, Jianying,Xi, Zhaoxia,Wang
Journal of medical genetics · 2024-03-21
pmid:379233807
Clinical and neuroimaging review of triplet repeat diseases.
Ryo,Kurokawa, Mariko,Kurokawa, Akihiko,Mitsutake, Moto,Nakaya, Akira,Baba, Yasuhiro,Nakata, Toshio,Moritani, Osamu,Abe
Japanese journal of radiology · 2022-09-28
pmid:361697688
CGG/CCG Repeat Expansions in
Sunsanee,Pongpakdee, Metha,Apiwattanakul, Thanes,Termglinchan, Rawiphan,Witoonpanich, Charungthai,Dejthevaporn, Theeraphong,Lee, Supika,Wansophonkul, Ai,Yamanaka, Shunsuke,Funaguma, Aritoshi,Lida, Ichizo,Nishino
Neurology. Genetics · 2024-07-08
pmid:39308795Additional 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)
CGG repeat expansions in Charcot-Marie-Tooth disease: insights from the 100 000 Genomes Project.
Alessandro,Bertini, Stefano,Facchini, Ilaria,Quartesan, Riccardo,Currò, Ricardo Parolin,Schnekenberg, Natalia,Dominik, Gustavo,Alves, Lucia,Ferullo, Arianna,Tucci, Henry,Houlden, Mary M,Reilly, Andrea,Cortese
Journal of neurology, neurosurgery, and psychiatry · 2026-05-14
pmid:40645757CGG/CCG Repeat Expansions in
Sunsanee,Pongpakdee, Metha,Apiwattanakul, Thanes,Termglinchan, Rawiphan,Witoonpanich, Charungthai,Dejthevaporn, Theeraphong,Lee, Supika,Wansophonkul, Ai,Yamanaka, Shunsuke,Funaguma, Aritoshi,Lida, Ichizo,Nishino
Neurology. Genetics · 2024-07-08
pmid:39308795GIPC1 CGG Repeat Expansion Is Associated with Movement Disorders.
Yu,Fan, Si,Shen, Jing,Yang, Dabao,Yao, Mengjie,Li, Chengyuan,Mao, Yunchao,Wang, Xiaoyan,Hao, Dongrui,Ma, Jiadi,Li, Jingjing,Shi, Mengnan,Guo, Shuangjie,Li, Yanpeng,Yuan, Fen,Liu, Zhihua,Yang, Shuo,Zhang, Zhengwei,Hu, Liyuan,Fan, Han,Liu, Chan,Zhang, Yanlin,Wang, Qingzhi,Wang, Hong,Zheng, Ying,He, Bo,Song, Yuming,Xu, Changhe,Shi
Annals of neurology · 2022-03-08
pmid:35152460