trimeric intracellular cation channel type B isoform X2 [Homo sapiens]

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Absence of the ER Cation Channel TMEM38B/TRIC-B Disrupts Intracellular Calcium Homeostasis and Dysregulates Collagen Synthesis in Recessive Osteogenesis Imperfecta. [PLoS Genet. 2016]
Absence of the ER Cation Channel TMEM38B/TRIC-B Disrupts Intracellular Calcium Homeostasis and Dysregulates Collagen Synthesis in Recessive Osteogenesis Imperfecta.
Cabral WA, Ishikawa M, Garten M, Makareeva EN, Sargent BM, Weis M, Barnes AM, Webb EA, Shaw NJ, Ala-Kokko L, et al. PLoS Genet. 2016 Jul; 12(7):e1006156. Epub 2016 Jul 21.
Two novel mutations in TMEM38B result in rare autosomal recessive osteogenesis imperfecta. [J Hum Genet. 2016]
Two novel mutations in TMEM38B result in rare autosomal recessive osteogenesis imperfecta.
Lv F, Xu XJ, Wang JY, Liu Y, Asan, Wang JW, Song LJ, Song YW, Jiang Y, Wang O, et al. J Hum Genet. 2016 Jun; 61(6):539-45. Epub 2016 Feb 25.
A deletion mutation in TMEM38B associated with autosomal recessive osteogenesis imperfecta. [Hum Mutat. 2013]
A deletion mutation in TMEM38B associated with autosomal recessive osteogenesis imperfecta.
Volodarsky M, Markus B, Cohen I, Staretz-Chacham O, Flusser H, Landau D, Shelef I, Langer Y, Birk OS. Hum Mutat. 2013 Apr; 34(4):582-6.

RefSeq genomic sequence
See the genomic reference sequence for the TMEM38B gene (NG_032971.1).
RefSeq mRNA
See reference mRNA sequence for the TMEM38B gene (XM_011518831.3).

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trimeric intracellular cation channel type B isoform X2 [Homo sapiens]
trimeric intracellular cation channel type B isoform X2 [Homo sapiens]
gi|767957817|ref|XP_011517133.1|

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