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Solute carrier family 17 member 9

WebThe gene for HP59 contains, entirely within its coding region, the Sialin Gene SLC17A5. Member 5, also known as SLC17A5 or sialin is a lysosomal membrane sialic acid transport protein which in humans is encoded by the SLC17A5 gene on Chromosome 6 [9] [10] [11] WebChromosome: 17. Map Location: 17 A1 17 8.61 cM. Summary: Related Services of SLC22A2 CRISPR guide RNA. mRNA Protein Product Price Select: NM_013667.2: NP_038695.1: solute carrier family 22 member 2: starting from $99.00: NM_013667.3: ... solute carrier family 22 member 2 isoform X1: starting from $99.00:

Solute carrier family - Wikipedia

WebJan 5, 2024 · Orthologous to human SLC17A9 (solute carrier family 17 member 9). [provided by Alliance of Genome Resources, Apr 2024] Other designations. solute carrier … WebMay 24, 2004 · Solute carrier family 17 member 9. Gene names. Name. SLC17A9. Synonyms. C20orf59. Organism names. Organism. Homo sapiens (Human) Taxonomic … firth of tay sure is choppy crossword https://bavarianintlprep.com

SLC35E3 Gene - GeneCards S35E3 Protein S35E3 Antibody

WebMay 26, 2016 · 182309 - solute carrier family 34 (type ii sodium/phosphate cotransporter), member 1; slc34a1 - solute carrier family 17, member 2, formerly; slc17a2, formerly;; sodium/phosphate transport 2, kidney; npt2;; renal sodium/phosphate transport protein 2;; … WebFeb 2, 2024 · Recently, we have identified seven genes that have prognostic power for the overall survival in OC, namely Guanylate Binding Protein 5 (GBP5), Insulin Receptor Substrate 2 (IRS2), Keratin 4 (KRT4), long intergenic non-protein coding RNA 707 (LINC00707), Mitochondrial Ribosomal Protein L55 (MRPL55), Ribosome Biogenesis Regulator 1 … WebDec 14, 2024 · Solute carrier family 15 (SLC15) members are H +-coupled oligopeptide cotransporters. SLC15A2 (also known as PEPT2) and SLC15A4 (also known as PHT1) are two representatives that transport nucleotide-binding oligomerization domain containing 2 (NOD2) ligands in the plasma membrane of epithelial cells and innate immune cells, like … firth of forth scotland map

SOLUTE CARRIER FAMILY 17 (ACIDIC SUGAR TRANSPORTER), …

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Solute carrier family 17 member 9

LOC111966661 solute carrier family 17 member 9 [ (Arctic char)]

WebTNF Family; Cytokines & Cytokine Receptors; Growth Factor; Cell Culture Related; Biosimilar Drug Targets; Tool proteins; Other Recombinant Protein; NGS Library Prep. DNA Library Prep; RNA Library Prep; Adapters; NGS Related Products; Clinical Consumables & Raw Materials. COVID-19 Sample Collection; Saliva Collection; Blood Collection; Urine ... Websolute carrier family 2, facilitated glucose transporter member 8 isoform 2: starting from $99.00: NM_019488.5: NP_062361.1: solute carrier family 2, facilitated glucose transporter member 8 isoform 1: starting from $99.00: NM_019488.4: NP_062361.1: solute carrier family 2, facilitated glucose transporter member 8: starting from $99.00

Solute carrier family 17 member 9

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WebJul 13, 2010 · Solute carrier family 2, facilitated glucose transporter member 9 Curated. Alternative names. Glucose transporter type 9 1 publication (GLUT-9 1 publication) Urate … Webアズワンの【AXEL】84-5065-22 SLC5A9 (Sodium/glucose Cotransporter 4, Solute Carrier Family 5 (Sodium/glucose Cotransporter), Member 9) 100ul 492161のコーナーです。AXELは研究開発、医療介護、生産現場、食品衛生など幅広い分野に750万点以上の品揃えでお応えする商品サイト。3000円以上ご注文で送料無料。

Web非结合性 17; Alexa Fluor 488 1; ... ch211-240l14.4 antibody, zgc:92098 antibody, 2310024J23Rik antibody, AL024256 antibody, solute carrier family 30 member 9 antibody, solute carrier family 30 (zinc transporter), member 9 antibody, ZIP metal ion transporter family antibody, solute carrier family 30 (zinc transporter), ... WebSep 1, 2024 · SLC7A11 (Solute Carrier Family 7 Member 11, xCT) forms system cystine/glutamate antiporter (x c-) with CD98 and is mainly expressed in the brain, macrophages, and cell lines, and acts as a Na +-independent transporter of extracellular anionic cystine and intracellular glutamate (Fotiadis et al., 2013).

WebGene ID: 107656994, updated on 13-Jun-2024. Summary Other designations. solute carrier family 17 member 9-like WebApr 19, 2012 · In affected members of an Iranian family with thiamine-responsive megaloblastic anemia syndrome (TRMA; 249270 ), Diaz et al. (1999) identified a 2-bp deletion involving 429T and 430T of the SLC19A2 gene. Three affected members of the family were studied and found to be homozygous. Two sets of parents and 1 unaffected …

WebSep 22, 2024 · SLC17A9 solute carrier family 17 member 9 Gene ID: 63910, updated on 22-Sep-2024 Gene type: protein coding Also known as: ... This gene encodes a member of a …

WebMar 21, 2024 · GeneCards Summary for SLC35E3 Gene. SLC35E3 (Solute Carrier Family 35 Member E3) is a Protein Coding gene. Diseases associated with SLC35E3 include Congenital Disorder Of Glycosylation, Type Iic and Cardiac Valvular Dysplasia, X-Linked . An important paralog of this gene is SLC35E2B. firth of forth special protection areaWebJun 1, 2001 · Recommended name. Solute carrier family 12 member 9. Alternative names. Cation-chloride cotransporter 6 ( hCCC6) Cation-chloride cotransporter-interacting protein … firth of forth sightseeing cruiseWebNov 27, 2024 · The transport of materials across membranes is a vital process for all aspects of cellular function, including growth, metabolism, and communication. Protein transporters are the molecular gates that control this movement and serve as key points of regulation for these processes, thus representing an attractive class of therapeutic … firth of forth offshore wind farmcamping l\u0027hermitage de chevignyWebSolute carrier family 22 member 9 is a protein that in humans is encoded by the SLC22A9 gene. See also. SLC22A9+protein,+human at the US National Library of Medicine Medical Subject Headings (MeSH) ... This page was last edited … firth of solwayWebMar 4, 2024 · SLC17A9 (solute carrier family 17 member 9) functions as an ATP transporter in lysosomes as well as other secretory vesicles. SLC17A9 inhibition or silence leads to … firth of tay bridgeWebSep 18, 2024 · In 6 affected members of highly consanguineous Arab-Israeli family with renal hypouricemia-2 (RHUC2; 612076), originally reported by Bahat et al. (2009), Dinour et al. (2010) identified a homozygous c.224T-G transversion in the SLC2A9 gene, resulting in a leu75-to-arg (L75R) substitution at a conserved residue in the long isoform (L46R in the … camping lounger back pillow cushion