Solute carrier family 15 member 1
WebSLC15A1 solute carrier family 15 member 1 [ (human)] Susceptibility Loci in SLC15A1, UGT1A3, and CWC27 Genes Associated with Bladder Cancer in the Northeast Chinese... WebApr 12, 2024 · Western blot analysis of ferroptosis‑related proteins demonstrated that ACR decreased the expression of glutathione peroxidase 4, solute carrier family 7 member 11, transferrin receptor protein 1 and ferritin heavy chain 1 in chondrocytes whereas Fer‑1 abolished these effects.
Solute carrier family 15 member 1
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Peptide transporter 1 (PepT 1) also known as solute carrier family 15 member 1 (SLC15A1) is a protein that in humans is encoded by SLC15A1 gene. PepT 1 is a solute carrier for oligopeptides. It functions in renal oligopeptide reabsorption and in the intestines in a proton dependent way, hence acting like a cotransporter. WebSolute carrier family. The solute carrier ( SLC) group of membrane transport proteins include over 400 members organized into 66 families. [1] [2] Most members of the SLC group are located in the cell membrane. The SLC gene nomenclature system was originally proposed by the HUGO Gene Nomenclature Committee ( HGNC) and is the basis for the ...
WebOct 13, 2024 · Summary. This gene encodes an intestinal hydrogen peptide cotransporter that is a member of the solute carrier family 15. The encoded protein is localized to the … WebSLC30A9 antibody, DKFZp459N1726 antibody, huel antibody, znt9 antibody, gac63 antibody, znt-9 antibody, ATZIP9 antibody, F4I10.1 antibody, C4orf1 antibody, GAC63 antibody, HUEL antibody, ZNT9 antibody, ZnT9 antibody, si:ch211-240l14.4 antibody, zgc:92098 antibody, 2310024J23Rik antibody, AL024256 antibody, solute carrier family 30 member 9 ...
WebMar 21, 2024 · SLC15A3 (Solute Carrier Family 15 Member 3) is a Protein Coding gene. Diseases associated with SLC15A3 include Hypotrichosis 4.Among its related pathways are Transport of inorganic cations/anions … WebJan 24, 2024 · solute carrier family 15 member 1, intestinal H(+)/peptide cotransporter, intestinal peptide transporter PEPT1, peptide transporter 1, proton-coupled dipeptide …
WebApr 10, 2024 · For chronic liver injury, controls were perfused with 0.2 mL distilled water for 4 weeks and treated with corn oil (with or without 10% CCl 4, see above) at d 1, 3 and 5 of the week.The mice were given 100 and 200 mg/kg MFAEs orally for 4 weeks followed with 10% CCl 4 in low-dose and high-dose MFAEs groups [].Positive drug group were given 200 …
Web61 rows · Solute carrier family 15 member 1 Kind protein Organism Humans Protein. Name UniProt ID; Solute carrier family 15 member 1: P46059: Details: Drug Relations Drug … impurity\\u0027s guWebMar 21, 2024 · SLC15A1 (Solute Carrier Family 15 Member 1) is a Protein Coding gene. Diseases associated with SLC15A1 include Short Bowel Syndrome and Hartnup … impurity\u0027s gvimpurity\u0027s gsWebMar 21, 2024 · SLC15A5 (Solute Carrier Family 15 Member 5) is a Protein Coding gene. Diseases associated with SLC15A5 include Barre-Lieou Syndrome and Dicarboxylic … impurity\u0027s gtWebMonika Schweigel-Röntgen, Martin Kolisek, in Current Topics in Membranes, 2014. Abstract. The solute carrier family 41 (SLC41) encompasses three members A1, A2, and A3. Based … impurity\\u0027s gtWebSLC15A1. This gene encodes an intestinal hydrogen peptide cotransporter that is a member of the solute carrier family 15. The encoded protein is localized to the brush border … impurity\\u0027s gvWebAug 14, 2024 · In 3 individuals with hypomineralized amelogenesis imperfecta (AI2A5; 615887) from a consanguineous Pakistani family (AI-112), Parry et al. (2013) identified a homozygous c.1015C-T transition in exon 11 the SLC24A4 gene, resulting in an arg339-to-ter (R339X) substitution. The mutation is predicted to lead to nonsense-mediated decay … impurity\\u0027s gz