PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 33655698-8 2021 Histone-lysine N-methyltransferase 2 (KMT2) family members (KMT2A, KMT2C, and KMT2D) were frequently mutated in NSCLC tumors, and these mutations were associated with higher TMB and PD-L1 expression, as well as higher PD-L1+/TMB-H proportions. tyrosyl-lysine 8-14 lysine methyltransferase 2D Homo sapiens 78-83 32024448-8 2020 Seven patients also had somatic mutations in APC, and seven patients harbored somatic mutations in KMT2D, which encodes a lysine methyl transferase. tyrosyl-lysine 122-135 lysine methyltransferase 2D Homo sapiens 99-104 31813957-3 2020 The major cause of Kabuki syndrome are mutations in KMT2D, a gene encoding a histone H3 lysine 4 (H3K4) methyltransferase belonging to the group of chromatin modifiers. tyrosyl-lysine 88-96 lysine methyltransferase 2D Homo sapiens 52-57 31654559-1 2020 Kabuki syndrome (KS) is a disorder of epigenetic dysregulation due to heterozygous mutations in KMT2D or KDM6A, genes encoding a lysine-specific methyltransferase or demethylase, respectively. tyrosyl-lysine 129-135 lysine methyltransferase 2D Homo sapiens 96-101 31924266-1 2020 The type 2 lysine methyltransferases KMT2C and KMT2D are large, enzymatically active scaffold proteins that form the core of nuclear regulatory structures known as KMT2C/D COMPASS complexes (complex of proteins associating with Set1). tyrosyl-lysine 11-17 lysine methyltransferase 2D Homo sapiens 47-52