Solute carrier family 17 member 9

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

Slc17a9 Mouse Gene Details solute carrier family 17, member 9 ...

WebOct 24, 2014 · 612107 - SOLUTE CARRIER FAMILY 17 (VESICULAR NUCLEOTIDE TRANSPORTER), MEMBER 9; SLC17A9 ... (MFS) domain, general substrate transporter. … 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] sharon sala free books https://benwsteele.com

SLC17A9 solute carrier family 17 member 9 - NIH Genetic …

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. 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 … WebThe 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 official HGNC names of the … popworld leeds opening times

SLC30A9 antibody (ABIN1842031)

Category:Slc12a9 (solute carrier family 12, member 9) - Rat Genome Database

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Solute carrier family 17 member 9

Nutrients Free Full-Text Candidate Genes Involved in Beneficial …

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. 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 …

Solute carrier family 17 member 9

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http://www.informatics.jax.org/marker/MGI:1919107 WebSep 4, 2013 · solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2: rs224589: 12: solute carrier family 11 (proton-coupled divalent metal ion transporters), member 3: rs427020: 12: VDR: vitamin D (1,25- dihydroxyvitamin D3) receptor: rs7975232: 12: LAMP1: lysosomal-associated membrane protein 1: rs12871648: 13: …

Web105355 Ensembl ENSG00000124564 ENSMUSG00000036083 UniProt O00476 n/a RefSeq (mRNA) NM_006632 NM_001098486 NM_001164743 NM_134069 RefSeq (protein) NP_001091956 NP_006623 n/a Location (UCSC) Chr 6: 25.83 – 25.88 Mb Chr 13: 24.02 – 24.04 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Solute carrier … WebIPR044777 Solute carrier family 17 member 9-like. IPR005829 Sugar transporter, conserved site. Molecular Reagents less. All nucleic 33. cDNA 33. Microarray probesets 3. Other Accession IDs less. MGI:2670971 References more. Summaries. All …

WebAnti VGluT1 (vesicular glutamate transporte-1) pAb Antibody (Goat) [Catalog No.: NMD-MSFR106200, NMD-MSFR106210] 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 …

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.

sharon sala new releases 2021WebGene ID: 111966661, updated on 27-Feb-2024. Summary Other designations. solute carrier family 17 member 9 popworld london watling streetWebMar 21, 2024 · SLC16A9 (Solute Carrier Family 16 Member 9) is a Protein Coding gene. Diseases associated with SLC16A9 include Gout . Gene Ontology (GO) annotations … popworld liverpool addressWebSolute 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 … pop world gameWebsolute 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 popworld milton keynes photosWebsolute carrier family 12, member 9 : Slc12a9 : solute carrier family 12 (potassium/chloride transporters), member 9 : Nomenclature updated to reflect human and mouse … sharon saliba wess obituaryWeb24060 Ensembl ENSG00000164414 ENSMUSG00000028293 UniProt P78382 Q61420 RefSeq (mRNA) NM_006416 NM_001168398 NM_011895 RefSeq (protein) NP_001161870 NP_006407 NP_036025 Location (UCSC) Chr 6: 87.47 – 87.51 Mb Chr 4: 34.66 – 34.69 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse CMP-sialic acid transporter … popworld newcastle capacity