RecName: Full=Lysosome-associated membrane glycoprotein 2; Short=LAMP- - Protein

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Altered Splicing of LAMP2 in a Multigenerational Family from Latvia Affected by Danon Disease. [Medicina (Kaunas). 2024]
Altered Splicing of LAMP2 in a Multigenerational Family from Latvia Affected by Danon Disease.
Stavusis J, Micule I, Grinfelde I, Zdanovica A, Pudulis J, Valeina S, Sepetiene S, Lace B, Inashkina I. Medicina (Kaunas). 2024 Jan 5; 60(1). Epub 2024 Jan 5.
Comparative study of the steady-state subcellular distribution of lysosome-associated membrane glycoprotein-2 (LAMP-2) isoforms with GYXXΦ-type tyrosine-based motifs that interact differently with four adaptor protein (AP) complexes. [J Biochem. 2024]
Comparative study of the steady-state subcellular distribution of lysosome-associated membrane glycoprotein-2 (LAMP-2) isoforms with GYXXΦ-type tyrosine-based motifs that interact differently with four adaptor protein (AP) complexes.
Yamaguchi F, Sakane H, Akasaki K. J Biochem. 2024 Mar 4; 175(3):275-287.
Danon Disease: Entire LAMP2 Gene Deletion with Unusual Clinical Presentation-Case Report and Review of the Literature. [Genes (Basel). 2023]
Danon Disease: Entire LAMP2 Gene Deletion with Unusual Clinical Presentation-Case Report and Review of the Literature.
Shalata A, Bar-Shai M, Hadid Y, Mahroum M, Mintz H, Shalata ZE, Radzishevsky E, Genizi J, Lorber A, Ben-Yosef T, et al. Genes (Basel). 2023 Jul 27; 14(8). Epub 2023 Jul 27.

RefSeq genomic sequence
See the genomic reference sequence for the LAMP2 gene (NG_007995.1).
RefSeq protein isoforms
See 3 reference sequence protein isoforms for the LAMP2 gene.

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P13473 [Domain Mapping of Disease Mut...]
P13473
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
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reagent reviews [ExactAntigen/Labome]
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reagents [ExactAntigen/Labome]
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lysosome-associated membrane protein-2b (LAMP2b), alternatively spliced form of ...
lysosome-associated membrane protein-2b (LAMP2b), alternatively spliced form of h-lamp-2 [Homo sapiens]
gi|2340102|gb|AAB67313.1||gnl|WUGSC 318C15.1b

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