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KDELR1 (KDEL Endoplasmic Reticulum Protein Retention Receptor 1) is a Protein Coding gene. Diseases associated with KDELR1 include Syndromic X-Linked Intellectual Disability 94 and Myopathy, Centronuclear, 1. Among its related pathways are Transport to the Golgi and subsequent modification and Activation of cAMP-Dependent PKA. Gene Ontology (GO) annotations related to this gene include ER retention sequence binding and KDEL sequence binding. An important paralog of this gene is KDELR2.
100 µg
100 µg
100 µg
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