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Search Thermo Fisher Scientific
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Immunogen sequence: MYCSAECRLA ATEQYHQVLC PGPSQDDPLH PLNKLQEAWR SIHYPPETAS IMLMARMVAT VKQAKDKDRW IRLFSQFCNK TANEEEEIVH KLLGDKFKG
Highest antigen sequence identity to the following orthologs: Mouse - 82%, Rat - 91%.
Retinoic acid (RA) represents the oxidized form of vitamin A and, via interactions with retinoic acid receptors (RARs), plays a crucial role in development, cellular growth and differentiation. The gene encoding RAI15 maps to human chromosome 2, which houses over 1,400 genes and comprises nearly 8% of the human genome. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene, while the lipid metabolic disorder sitosterolemia is associated with defects in the ABCG5 and ABCG8 genes. Additionally, an extremely rare recessive genetic disorder, Alström syndrome, is caused by mutations in the ALMS1 gene, which maps to chromosome 2.
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Protein Aliases: [histone H4]-lysine20 N-trimethyltransferase SMYD5; Histone-lysine N-trimethyltransferase SMYD5; Protein NN8 4AG; Protein NN8-4AG; retinoic acid induced 15; retinoic acid responsive; Retinoic acid-induced protein 15; SET and MYND domain-containing protein 5
Gene Aliases: NN8-4AG; RAI15; RRG1; SMYD5; ZMYND23
UniProt ID: (Human) Q6GMV2
Entrez Gene ID: (Human) 10322
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