Solute carrier family 35 member e3
WebSLC35F6 → Solute carrier family 35 member F6. Protein also known as : Transport and Golgi organization 9 homolog . Gene name : SLC35F6. Family name : SLC35F solute transporter. Entry whose protein (s) existence is based on evidence at protein level. Displayed isoform: Iso 1. WebSolute carrier family members control essential physiological functions and are tightly linked to human diseases. Solute carrier family 35 member F2 (SLC35F2) is aberrantly activated in several malignancies. However, the biological function and molecular mechanism of SLC35F2 in papillary thyroid carcinoma (PTC) are yet to be fully explored.
Solute carrier family 35 member e3
Did you know?
WebTocopherol (alpha) transfer protein (ataxia (Friedreich-like) with vitamin E deficiency) WebMar 15, 2024 · Microarray data analysis showed that some ferroptosis genes are associated with HCM, such as ATF3, LPCAT3, and solute carrier family 1 member 5 (SLC1A5) . Diabetic Cardiomyopathy. DCM is a pathophysiological condition caused by diabetes that contributes to HF where the decline of myocardial cell function is an important mediating mechanism .
WebGene ID: 104989770, updated on 2-Feb-2024. Summary Other designations. solute carrier family 35 member E3 WebS35E4_HUMAN RecName: Full=Solute carrier family 35 member E4. 0 0 0 0 0 Tips: The Domains on the Default View are decided by the Domain's E-Value. Clicking a check box will display or hide the correlated domain. To view the Gene page, either click on the link to the left or the blue bar above the Protein's graphic. Default ...
WebRecombinant protein of human solute carrier family 35, member A4 (SLC35A4) Supplier Page. Supplier Page from OriGene Technologies for SLC35A4 (NM_080670) Human Recombinant Protein. ... Gene Name solute carrier family 35, member A4; NCBI Full Gene Name solute carrier family 35 member A4; Add to Compare List. WebMar 21, 2024 · SLC35E3 (Solute Carrier Family 35 Member E3) is a Protein Coding gene. Diseases associated with SLC35E3 include Congenital Disorder Of Glycosylation, Type Iic …
WebMar 21, 2024 · GeneCards Summary for SLC35E1 Gene. SLC35E1 (Solute Carrier Family 35 Member E1) is a Protein Coding gene. Diseases associated with SLC35E1 include …
WebSep 15, 2024 · In some embodiments, the activating AR mutation is selected from one or more of one or more of AR gene amplification, one or more activating mutations in the ligand binding domain of AR (optionally selected from H874Y, T877A, T877S, T878A, and F876L), an AR splice variant lacking the ligand binding domain of AR (optionally ARV7 or … lithium americas websiteWebA 22-year-old man was admitted with complaints of dyspnea and hoarseness. Laryngoscopy and computed tomography of the neck revealed a 1.5 x 2-cm solid mass obstructing the trachea. lithium americas winnemucca nvWebOrthologous to human SLC35E3 (solute carrier family 35 member E3). [provided by Alliance of Genome Resources, Apr 2024] Slc35e3 solute carrier family 35, member E3 [ (house … lithium americas ticker symbolWebPR:000015103 solute carrier family 35 member E3 (term hierarchy) InterPro Domains. IPR004853 Sugar phosphate transporter domain. Molecular Reagents less. All nucleic 36. … lithium americas twitterWebSolute carrier family 38 member 9 (SLC38A9) transports leucine from lysosomes into the cytoplasm. Wyant et al 45 found that in cells lacking SLC38A9, lysosomal leucine levels remained essentially unchanged, even though whole-cell leucine levels were reduced compared to the control. lithium americorpWebIPR009262 Solute carrier family 35 member SLC35F1/F2/F6. Molecular Reagents less. All nucleic 16. cDNA 16. Microarray probesets 6. Other Accession IDs less. MGI:2441700 References more. Summaries. All 53. Diseases 1. Gene Ontology 4. Phenotypes 30. Earliest. J:5021 Batchelor AL, et al., improve ssd speedWebsolute carrier family 35, member E2. Synonyms: A530082C11Rik. Order Alleles. IMPC Data Collections. Body Weight Measurements ; ... 5.35% (32 of 598) ... All available products … improve ssis package performance