Homo sapiens mRNA; cDNA DKFZp686K0887 (from clone DKFZp686K0887)

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Dual proteome-scale networks reveal cell-specific remodeling of the human interactome. [Cell. 2021]
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
Huttlin EL, Bruckner RJ, Navarrete-Perea J, Cannon JR, Baltier K, Gebreab F, Gygi MP, Thornock A, Zarraga G, Tam S, et al. Cell. 2021 May 27; 184(11):3022-3040.e28. Epub 2021 May 6.
Pathogenic variants in IMPG1 cause autosomal dominant and autosomal recessive retinitis pigmentosa. [J Med Genet. 2021]
Pathogenic variants in IMPG1 cause autosomal dominant and autosomal recessive retinitis pigmentosa.
Olivier G, Corton M, Intartaglia D, Verbakel SK, Sergouniotis PI, Le Meur G, Dhaenens CM, Naacke H, Avila-Fernández A, Hoyng CB, et al. J Med Genet. 2021 Aug; 58(8):570-578. Epub 2020 Aug 17.
UNUSUAL EARLY-ONSET VITELLIFORM DYSTROPHY POSSIBLY LINKED TO THE INTERPHOTORECEPTOR MATRIX PROTEOGLYCAN-1 P.LEU154PRO MUTATION. [Retin Cases Brief Rep. 2021]
UNUSUAL EARLY-ONSET VITELLIFORM DYSTROPHY POSSIBLY LINKED TO THE INTERPHOTORECEPTOR MATRIX PROTEOGLYCAN-1 P.LEU154PRO MUTATION.
Gupta MP, Brodie SE, Freund KB. Retin Cases Brief Rep. 2021 Sep 1; 15(5):527-531.

RefSeq alternative splicing
See 2 reference mRNA sequence splice variants for the IMPG1 gene.

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Nucleotide