Locus OPDM4 RILPL1

Disease ID
OPDM4
Gene ID
RILPL1
Updated
Jun 15, 2026
v2.22.0
Other gene loci
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Disease

Name Oculopharyngodistal myopathy type 4
Inheritance
Description
Ptosis, external ophthalmoplegia, facial weakness, and pharyngeal and distal limb weakness .
Prevalence
Population dependent: 21.6% of one OPDM cohort . Typically found in individuals of East Asian ancestry .
Age of Onset Age of Onset(Typical)Years10  3018  30
Typical: 18-30 ; Range: 10-30 .
HPO Terms
Association
Mendelian

Locus

Details
Benign alleles have been documented to have 6-16 repeats , while pathogenic repeats range from 120 to 197 repeats; there is no apparent relationship between allele size and age of onset, . Intermediate alleles may be associated with incomplete penetrance, or milder phenotypes . AGG, TGG, and CGT interruptions observed, .
Mechanism
GoF
Polyglutamine expansion leading to RNA-mediated gain-of-function mechanism .
Detection
Year
2022
Location in Gene
5' UTR
Gene Strand

Alleles

Ref. Motif
GGC
Ranges BenignIntermediatePathogenicUnits6  160  0120  197
Benign (ref.)
Benign (gene)
Pathogenic (ref.)
GGC
Pathogenic (gene)
CCG
Unknown (ref.)
Unknown (gene)
Interruption (ref.)
TGG, CGT, AGG
Interruption (gene)
ACC, ACG, CCT

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:38876750
2
The CGG repeat expansion in RILPL1 is associated with oculopharyngodistal myopathy type 4.
Jiaxi,Yu, Jingli,Shan, Meng,Yu, Li,Di, Zhiying,Xie, Wei,Zhang, He,Lv, Lingchao,Meng, Yiming,Zheng, Yawen,Zhao, Qiang,Gang, Xueyu,Guo, Yang,Wang, Jianying,Xi, Wenhua,Zhu, Yuwei,Da, Daojun,Hong, Yun,Yuan, Chuanzhu,Yan, Zhaoxia,Wang, Jianwen,Deng
American journal of human genetics · 2022-02-10
pmid:35148830
3
GGC Repeat Expansion of RILPL1 is Associated with Oculopharyngodistal Myopathy.
Yi-Heng,Zeng, Kang,Yang, Gan-Qin,Du, Yi-Kun,Chen, Chun-Yan,Cao, Yu-Sen,Qiu, Jin,He, Hai-Dong,Lv, Qian-Qian,Qu, Jian-Nan,Chen, Guo-Rong,Xu, Long,Chen, Fu-Ze,Zheng, Miao,Zhao, Min-Ting,Lin, Wan-Jin,Chen, Jing,Hu, Zhi-Qiang,Wang, Ning,Wang
Annals of neurology · 2022-07-02
pmid:35700120
4
A large pedigree study confirmed the CGG repeat expansion of RILPL1 Is associated with oculopharyngodistal myopathy.
Xinzhuang,Yang, Dingding,Zhang, Si,Shen, Pidong,Li, Mengjie,Li, Jingwen,Niu, Dongrui,Ma, Dan,Xu, Shuangjie,Li, Xueyu,Guo, Zhen,Wang, Yanhuan,Zhao, Haitao,Ren, Chao,Ling, Yang,Wang, Yu,Fan, Jianxiong,Shen, Yicheng,Zhu, Depeng,Wang, Liying,Cui, Lin,Chen, Changhe,Shi, Yi,Dai
BMC medical genomics · 2023-10-20
pmid:37864208
5
Sequence composition changes in short tandem repeats: heterogeneity, detection, mechanisms and clinical implications.
Indhu-Shree,Rajan-Babu, Egor,Dolzhenko, Michael A,Eberle, Jan M,Friedman
Nature reviews. Genetics · 2024-03-11
pmid:38467784

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)

Translation of expanded CGG repeats in LRP12 associated oculopharyngodistal myopathy.
Chengcheng,Li, Jil A,Daw, Sara K,Pittman, Connor J,Maltby, Hidetoshi,Sakurai, Peter K,Todd, Conrad C,Weihl
Acta neuropathologica communications · 2026-03-06
pmid:41792844
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:40645757
A case report of oculopharyngodistal myopathy with 126 CGG repeat expansions in
Wenjing,Wang, Tielun,Yin, Xinyu,Zhang, Zhaoxia,Wang, Tianyun,Wang, Shuo,Zhang, Yingshuang,Zhang, Dongsheng,Fan
Frontiers in genetics · 2025-02-27
pmid:40084170
Clinical and pathological characteristics of OPDM4 patients in advanced disease.
Haixia,Tang, Ying,Xiong, Kaiyan,Jiang, Yu,Shen, Yanyan,Yu, Pengcheng,Huang, Min,Zhu, Xiaobing,Li, Yilei,Zheng, Meihong,Zhou, Jiaxi,Yu, Jianwen,Deng, Zhaoxia,Wang, Daojun,Hong, Yusen,Qiu, Dandan,Tan
Muscle & nerve · 2024-07-23
pmid:39044557
Linking LRP12 CGG repeat expansion to inherited peripheral neuropathy.
Takahiro,Hobara, Masahiro,Ando, Yujiro,Higuchi, Jun-Hui,Yuan, Akiko,Yoshimura, Fumikazu,Kojima, Yutaka,Noguchi, Jun,Takei, Yu,Hiramatsu, Satoshi,Nozuma, Tomonori,Nakamura, Tadashi,Adachi, Keiko,Toyooka, Toru,Yamashita, Yusuke,Sakiyama, Akihiro,Hashiguchi, Eiji,Matsuura, Yuji,Okamoto, Hiroshi,Takashima
Journal of neurology, neurosurgery, and psychiatry · 2025-01-16
pmid:39013564
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:37923380