FAME1 SAMD12
Disease ID
FAME1
Gene ID
SAMD12
Disease
Name
Familial adult myoclonic epilepsy type 1
Inheritance
Autosomal dominant Description
Prevalence
Locus
Details
Alleles
Ref. Motif
TAAAA
Pathogenic (ref.)
TGAAA
Pathogenic (gene)
ATTTC
Unknown (ref.)
AAAAA, TAAAC, TAACA, TACAA, TACAC
Unknown (gene)
TTTTT, AGTTT, ATGTT, ATTGT, AGTGT
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 · 2024-09-30
pmid:393490433
Intronic pentanucleotide TTTCA repeat insertion in the SAMD12 gene causes familial cortical myoclonic tremor with epilepsy type 1.
Zhidong,Cen, Zhengwen,Jiang, You,Chen, Xiaosheng,Zheng, Fei,Xie, Xiaodong,Yang, Xingjiao,Lu, Zhiyuan,Ouyang, Hongwei,Wu, Si,Chen, Houmin,Yin, Xia,Qiu, Shuang,Wang, Meiping,Ding, Yelei,Tang, Feng,Yu, Caihua,Li, Tao,Wang, Hiroyuki,Ishiura, Shoji,Tsuji, Chuan,Jiao, Chunyu,Liu, Jianfeng,Xiao, Wei,Luo
Brain : a journal of neurology · 2018-08-01
pmid:299392034
Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy.
Hiroyuki,Ishiura, Koichiro,Doi, Jun,Mitsui, Jun,Yoshimura, Miho Kawabe,Matsukawa, Asao,Fujiyama, Yasuko,Toyoshima, Akiyoshi,Kakita, Hitoshi,Takahashi, Yutaka,Suzuki, Sumio,Sugano, Wei,Qu, Kazuki,Ichikawa, Hideaki,Yurino, Koichiro,Higasa, Shota,Shibata, Aki,Mitsue, Masaki,Tanaka, Yaeko,Ichikawa, Yuji,Takahashi, Hidetoshi,Date, Takashi,Matsukawa, Junko,Kanda, Fumiko Kusunoki,Nakamoto, Mana,Higashihara, Koji,Abe, Ryoko,Koike, Mutsuo,Sasagawa, Yasuko,Kuroha, Naoya,Hasegawa, Norio,Kanesawa, Takayuki,Kondo, Takefumi,Hitomi, Masayoshi,Tada, Hiroki,Takano, Yutaka,Saito, Kazuhiro,Sanpei, Osamu,Onodera, Masatoyo,Nishizawa, Masayuki,Nakamura, Takeshi,Yasuda, Yoshio,Sakiyama, Mieko,Otsuka, Akira,Ueki, Ken-Ichi,Kaida, Jun,Shimizu, Ritsuko,Hanajima, Toshihiro,Hayashi, Yasuo,Terao, Satomi,Inomata-Terada, Masashi,Hamada, Yuichiro,Shirota, Akatsuki,Kubota, Yoshikazu,Ugawa, Kishin,Koh, Yoshihisa,Takiyama, Natsumi,Ohsawa-Yoshida, Shoichi,Ishiura, Ryo,Yamasaki, Akira,Tamaoka, Hiroshi,Akiyama, Taisuke,Otsuki, Akira,Sano, Akio,Ikeda, Jun,Goto, Shinichi,Morishita, Shoji,Tsuji
Nature genetics · 2018-03-05
pmid:295074235
(TTTCA)exp Drives the Genotype-Phenotype Correlation and Genetic Anticipation in FCMTE1.
Xinhui,Chen, Bo,Wang, Haibin,Xia, Haotian,Wang, Dehao,Yang, Miao,Chen, Huijun,Yu, Fan,Zhang, Yixin,Kang, Yiling,Chen, Nan,Jin, Lebo,Wang, Peng,Liu, Fei,Xie, Aisi,Fu, Ben,Hu, Zhiyuan,Ouyang, Sheng,Wu, Yao,Ding, Junfeng,Ji, Shuang,Wang, Wei,Luo, Zhidong,Cen
Movement disorders : official journal of the Movement Disorder Society · 2024-11-21
pmid:395698767
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:38467784Additional 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)
Tremor-associated short tandem repeat intermediate and pathogenic expansions in familial essential tremor.
Xun,Zhou, Runcheng,He, Sheng,Zeng, Mingqiang,Li, Hongxu,Pan, Yuwen,Zhao, Zhenhua,Liu, Qian,Xu, Jifeng,Guo, Xinxiang,Yan, Jinchen,Li, Beisha,Tang, Qiying,Sun
Brain communications · 2024-06-29
pmid:38961870Origin and evolution of pentanucleotide repeat expansions at the familial cortical myoclonic tremor with epilepsy type1 - SAMD12 locus.
Xinhui,Chen, Fan,Zhang, Yihua,Shi, Haotian,Wang, Miao,Chen, Dehao,Yang, Lebo,Wang, Peng,Liu, Fei,Xie, Jiawen,Chen, Aisi,Fu, Ben,Hu, Bo,Wang, Zhiyuan,Ouyang, Sheng,Wu, Zhiru,Lin, Zhidong,Cen, Wei,Luo
European journal of human genetics : EJHG · 2024-03-12
pmid:38467733Seizures and electrophysiological features in familial cortical myoclonic tremor with epilepsy 1.
Yao,Ding, Zhidong,Cen, Yang,Zheng, Xia,Qiu, Yumao,Ye, Xinhui,Chen, Lingli,Hu, Bo,Wang, Zhongjin,Wang, Houmin,Yin, Chunhong,Shen, Wenjie,Ming, Yi,Ge, Fei,Xie, Dehao,Yang, Zhiyuan,Ouyang, Haotian,Wang, Sheng,Wu, Meiping,Ding, Shuang,Wang, Wei,Luo
Annals of clinical and translational neurology · 2023-12-07
pmid:38059543Complete SAMD12 repeat expansion sequencing in a four-generation BAFME1 family with anticipation.
Takeshi,Mizuguchi, Tomoko,Toyota, Eriko,Koshimizu, Shinichi,Kameyama, Hiromi,Fukuda, Naomi,Tsuchida, Yuri,Uchiyama, Kohei,Hamanaka, Atsushi,Fujita, Kazuharu,Misawa, Satoko,Miyatake, Hiroaki,Adachi, Naomichi,Matsumoto
Journal of human genetics · 2023-08-18
pmid:37592133A novel FAME1 repeat configuration in a European family identified using a combined genomics approach.
Tatiana,Maroilley, Meng-Han,Tsai, Rumika,Mascarenhas, Catherine,Diao, Maryam,Khanbabaei, Sabine,Kaya, Christel,Depienne, Maja,Tarailo-Graovac, Karl Martin,Klein
Epilepsia open · 2023-02-16
pmid:36740228Insights into familial adult myoclonus epilepsy pathogenesis: How the same repeat expansion in six unrelated genes may lead to cortical excitability.
Christel,Depienne, Arn M J M,van den Maagdenberg, Theresa,Kühnel, Hiroyuki,Ishiura, Mark A,Corbett, Shoji,Tsuji
Epilepsia · 2023-01-22
pmid:36622139ATTCT and ATTCC repeat expansions in the ATXN10 gene affect disease penetrance of spinocerebellar ataxia type 10.
C Alejandra,Morato Torres, Faria,Zafar, Yu-Chih,Tsai, Jocelyn Palafox,Vazquez, Michael D,Gallagher, Ian,McLaughlin, Karl,Hong, Jill,Lai, Joyce,Lee, Amanda,Chirino-Perez, Angel Omar,Romero-Molina, Francisco,Torres, Juan,Fernandez-Ruiz, Tetsuo,Ashizawa, Janet,Ziegle, Francisco Javier,Jiménez Gil, Birgitt,Schüle
HGG advances · 2022-08-15
pmid:36092952Complete sequencing of expanded SAMD12 repeats by long-read sequencing and Cas9-mediated enrichment.
Takeshi,Mizuguchi, Tomoko,Toyota, Satoko,Miyatake, Satomi,Mitsuhashi, Hiroshi,Doi, Yosuke,Kudo, Hitaru,Kishida, Noriko,Hayashi, Rie S,Tsuburaya, Masako,Kinoshita, Tetsuhiro,Fukuyama, Hiromi,Fukuda, Eriko,Koshimizu, Naomi,Tsuchida, Yuri,Uchiyama, Atsushi,Fujita, Atsushi,Takata, Noriko,Miyake, Mitsuhiro,Kato, Fumiaki,Tanaka, Hiroaki,Adachi, Naomichi,Matsumoto
Brain : a journal of neurology · 2021-05-07
pmid:33791773Comprehensive genetic, clinical and electrophysiological studies of familial cortical myoclonic tremor with epilepsy 1 highlight the role of gene configurations.
Sipei,Pan, Xuying,Li, Liping,Li, Hua,Lin, Dequan,Wang, Xiating,Zhang, Xin,Zhao, Jing,Ye, Zhaoyang,Huang, Yicong,Lin, Yiran,Duan, Rui,Ma, Lehong,Gao, Chaodong,Wang, Yuping,Wang
Seizure · 2021-02-23
pmid:33721773