Solute carrier family 17 member 9

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August undefined, 2024

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 … WebUn-conjugated 17; Alexa Fluor 488 1; ... ch211-240l14.4 antibody, zgc:92098 antibody, 2310024J23Rik antibody, AL024256 antibody, solute carrier family 30 member 9 …

SLC35E3 Gene - GeneCards S35E3 Protein S35E3 Antibody

WebNov 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 … http://www.informatics.jax.org/marker/MGI:1919107 churchill retail park andover

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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 … WebOther members work as antiporters (exchangers) that typically contain a single substrate-binding site with an alternating access mode of transport, while a few members exhibit channel-like properties. Dysfunction of SLCs is correlated with numerous human diseases and therefore they are potential therapeutic drug targets. WebDec 1, 2010 · SLC9A3R1 is a cytoplasmic protein. SLC9A3R1 translocates from the cytoplasm to the apical cell membrane in a PODXL-dependent manner. SLC9A3R1 colocalizes with actin in microvilli-rich apical regions of the syncytiotrophoblast. SLC9A3R1 has been found in microvilli, ruffling membrane and filopodia of HeLa cells. churchill results today

Solute carrier transporters: the metabolic gatekeepers of immune …

Slc17a9 (solute carrier family 17 member 9) - Rat Genome Database

WebMar 21, 2024 · SLC16A9 (Solute Carrier Family 16 Member 9) is a Protein Coding gene. Diseases associated with SLC16A9 include Gout . Gene Ontology (GO) annotations … WebSep 12, 2024 · Despite some members of the SLC superfamily displaying weak sequence similarities and even though much structural knowledge still needs to be elucidated, solute carriers show some common structural features [1, 7, 11].Most members of this superfamily locate in the cell membrane, though some of them are found in the mitochondria or other … churchill retirement banburyWebJul 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 … churchill restaurant north bay ontario

"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 17 member 9

Solute carrier family 17 member 9

SOLUTE CARRIER FAMILY 19 (THIAMINE TRANSPORTER), MEMBER 2; SLC19A2

WebMar 29, 2024 · SLC17A6 solute carrier family 17 member 6 [ (human)] Gene ID: 57084, updated on 29-Mar-2024. Summary. Predicted to enable ... solute carrier family 17 … WebSolute 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 …

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WebAug 14, 2024 · 609840 - SOLUTE CARRIER FAMILY 24 (SODIUM/POTASSIUM/CALCIUM EXCHANGER), MEMBER 4; SLC24A4 - SODIUM/POTASSIUM/CALCIUM EXCHANGER 4; NCKX4 ... Pedersen et al. (2024) identified a 21-bp duplication in exon 17 of the SLC24A4 gene as the cause of AI in Samoyeds. WebApr 28, 2024 · In an African-American girl, born of unrelated parents, with BILAPES, Kleyner et al. (2024) identified compound heterozygous frameshift mutations in the SLC30A9 gene ( 604604.0002 and 604604.0003 ). The mutations, which were found by whole-exome sequencing and confirmed by Sanger sequencing, were each inherited from an unaffected …

WebSLC9A3 solute carrier family 9 member A3 [ (takin)] Gene ID: 128066142, updated on 28-Feb-2024. Summary Other designations. sodium/hydrogen ... WebSep 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 …

WebMay 24, 2004 · Solute carrier family 17 member 9. Gene names. Name. SLC17A9. Synonyms. C20orf59. Organism names. Organism. Homo sapiens (Human) Taxonomic … 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;; …

WebDec 8, 2024 · MFS_SLC17A5; Solute carrier family 17 member 5 (also called sialin) of the Major Facilitator Superfamily of transporters; NM_001382636.1 → NP_001369565.1 sialin …

churchill retirement bagshotWebSolute carrier family 9, subfamily A, member 3 (SLC9A3)/sodium-hydrogen exchanger member 3 (NHE3) dysregulation and dilated intercellular spaces in patients with … churchill restaurant alderley edgeWebsolute 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 churchill restaurant perthWebMar 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. churchill retirement abingdonWebJan 10, 2024 · Aims:The solute carrier family 2 (SLC2) genes are comprised of 14 members which are essential for the maintenance of glucose uptake and survival of tumour cells. This study was performed to investigate the associations of SLC2 family gene expression with mortality in acute myeloid leukemia (AML).Methods:Clinical features and SLC2 family … devon partnership trust jobsWebThe 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] devonpct.physiotoolsonlineWebApr 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 … churchill retirement aylesbury