MIR7-2 CHNG3
Disease ID
CHNG3
Gene ID
MIR7-2
Updated
Sep 5, 2025
v2.10.0
v2.10.0
Bioinformatical Links
Disease
Name
Nongoitrous congenital hypothyroidism-3
Inheritance
Autosomal dominant Description
Prevalence
Age of Onset Details
Locus
Details
Alleles
Ref. Motif
TTTG
Pathogenic (ref.)
TTTG
Pathogenic (gene)
AAAC
References
Direct supporting references for info on this page.
2
Functional variants in a TTTG microsatellite on 15q26.1 cause familial nonautoimmune thyroid abnormalities.
Satoshi,Narumi, Keisuke,Nagasaki, Mitsuo,Kiriya, Erika,Uehara, Kazuhisa,Akiba, Kanako,Tanase-Nakao, Kazuhiro,Shimura, Kiyomi,Abe, Chiho,Sugisawa, Tomohiro,Ishii, Kenichi,Miyako, Yukihiro,Hasegawa, Yoshihiro,Maruo, Koji,Muroya, Natsuko,Watanabe, Eijun,Nishihara, Yuka,Ito, Takahiko,Kogai, Kaori,Kameyama, Kazuhiko,Nakabayashi, Kenichiro,Hata, Maki,Fukami, Hirohito,Shima, Atsuo,Kikuchi, Jun,Takayama, Gen,Tamiya, Tomonobu,Hasegawa
Nature genetics · 2024-05-07
pmid:387148683
STR mutations on chromosome 15q cause thyrotropin resistance by activating a primate-specific enhancer of MIR7-2/MIR1179.
Helmut,Grasberger, Alexandra M,Dumitrescu, Xiao-Hui,Liao, Elliott G,Swanson, Roy E,Weiss, Panudda,Srichomkwun, Theodora,Pappa, Junfeng,Chen, Takashi,Yoshimura, Phillip,Hoffmann, Monica Malheiros,França, Rebecca,Tagett, Kazumichi,Onigata, Sabine,Costagliola, Jane,Ranchalis, Mitchell R,Vollger, Andrew B,Stergachis, Jessica X,Chong, Michael J,Bamshad, Guillaume,Smits, Gilbert,Vassart, Samuel,Refetoff
Nature genetics · 2024-05-07
pmid:38714869