Uniprot AC Entrez ID Gene Name Disease Cell Type PTM Type State Position PMID O76082 6584 SLC22A5 OCTN2 Renal carnitine transport defect Glycosylation N N57 O76082 6584 SLC22A5 OCTN2 Renal carnitine transport defect N-linked glycosylation N N57 O76082 6584 SLC22A5 OCTN2 Renal carnitine transport defect Glycosylation N N64 O76082 6584 SLC22A5 OCTN2 Systemic primary carnitine deficiency Phosphorylation N T88 O76082 6584 SLC22A5 OCTN2 Renal carnitine transport defect Glycosylation N N91 O76082 6584 SLC22A5 OCTN2 Renal carnitine transport defect N-linked glycosylation N N91 O76082 6584 SLC22A5 OCTN2 Systemic primary carnitine deficiency Phosphorylation N S93 O76082 6584 SLC22A5 OCTN2 Systemic primary carnitine deficiency Phosphorylation N T264 O76082 6584 SLC22A5 OCTN2 Colorectal adenocarcinoma Ubiquitination N K302 O76082 6584 SLC22A5 OCTN2 Renal carnitine transport defect Ubiquitination N K302 O76082 6584 SLC22A5 OCTN2 Systemic primary carnitine deficiency Ubiquitination N K302 O76082 6584 SLC22A5 OCTN2 Renal carnitine transport defect Ubiquitination N K324 O76082 6584 SLC22A5 OCTN2 Systemic primary carnitine deficiency Phosphorylation N T468 O76082 6584 SLC22A5 OCTN2 Systemic primary carnitine deficiency Phosphorylation N S470 O76082 6584 SLC22A5 OCTN2 Systemic primary carnitine deficiency Phosphorylation N S474 O76082 6584 SLC22A5 OCTN2 Breast invasive carcinoma Phosphorylation N Y486 O76082 6584 SLC22A5 OCTN2 Colon adenocarcinoma Phosphorylation N Y486 O76082 6584 SLC22A5 OCTN2 Renal carnitine transport defect Phosphorylation N Y486 O76082 6584 SLC22A5 OCTN2 Systemic primary carnitine deficiency Phosphorylation N Y486 O76082 6584 SLC22A5 OCTN2 Glioblastoma multiforme Ubiquitination N K543 O76082 6584 SLC22A5 OCTN2 Renal carnitine transport defect Ubiquitination N K543 O76082 6584 SLC22A5 OCTN2 Glioblastoma multiforme Phosphorylation N T550 O76082 6584 SLC22A5 OCTN2 Renal carnitine transport defect Phosphorylation N T550 O76082 6584 SLC22A5 OCTN2 Renal carnitine transport defect Ubiquitination N K553