immunoglobulin superfamily member 3 isoform X2 [Homo sapiens]

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IGSF3 mutation identified in patient with severe COPD alters cell function and motility. [JCI Insight. 2020]
IGSF3 mutation identified in patient with severe COPD alters cell function and motility.
Schweitzer KS, Jinawath N, Yonescu R, Ni K, Rush N, Charoensawan V, Bronova I, Berdyshev E, Leach SM, Gillenwater LA, et al. JCI Insight. 2020 Jul 23; 5(14). Epub 2020 Jul 23.
Congenital dacryocystocele: is there a familial predisposition? [Int J Pediatr Otorhinolaryngol...]
Congenital dacryocystocele: is there a familial predisposition?
Wang JC, Cunningham MJ. Int J Pediatr Otorhinolaryngol. 2011 Mar; 75(3):430-2. Epub 2010 Dec 23.
Prevalence and clinical characteristics of congenital dacryocystocele. [J AAPOS. 2010]
Prevalence and clinical characteristics of congenital dacryocystocele.
Shekunov J, Griepentrog GJ, Diehl NN, Mohney BG. J AAPOS. 2010 Oct; 14(5):417-20.

RefSeq genomic sequence
See the genomic reference sequence for the IGSF3 gene (NG_050917.1).
RefSeq mRNA
See reference mRNA sequence for the IGSF3 gene (XM_011541315.2).
RefSeq protein isoforms
See 16 reference sequence protein isoforms for the IGSF3 gene.

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Ensembl [Ensembl]
Ensembl
OncoMX cancer biomarker resource [OncoMX cancer biomarker resou...]
OncoMX cancer biomarker resource
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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