Solute carrier family 25 member 51-like

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August undefined, 2024

WebAug 26, 2024 · Microcephaly, Amish Type. Rosenberg et al. (2002) found a homozygous mutation in the SLC25A19 gene (G177A: 606521.0001) to be the cause of Amish-type microcephaly (MCPHA; 607196), also known as thiamine metabolism dysfunction syndrome-3 (THMD3). Thiamine Metabolism Dysfunction Syndrome 4. By homozygosity … WebFeb 5, 2024 · SLC25A15 solute carrier family 25 member 15 [ (human)] Gene ID: 10166, updated on 5-Feb-2024. Summary. This gene is a ... We suggest including HHH syndrome in the differential diagnosis of patients found to have stroke-like lesions on brain MRI. expression, reconstitution, ...

Immune Infiltrates in Hepatocellular Carcinoma JHC

WebMonika 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 on their distant homology to the bacterial Mg 2 + channel MgtE, all have been linked to Mg 2 + transport. There is only very limited knowledge on the molecular biology and exact … WebSolute carrier family 39 members (SLC39As) have been identified as zinc metal ion transporting proteins, and their dysregulation has been proven to induce cellular zinc dyshomeostasis and exhibit various oncogenic properties in multiple malignancies, such as lung, cervical, and pancreatic cancers. 6–11 For instance, SLC39A4 accelerates epithelial … bishopthorpe

The SLC25 Mitochondrial Carrier Family: Structure and …

WebApr 4, 2024 · The protein encoded by this gene belongs to the family of calcium-binding mitochondrial carriers, with a characteristic mitochondrial carrier domain at the C-terminus. These proteins are found in the inner membranes of mitochondria, and function as transport proteins. They shuttle metabolites, nucleotides and cofactors through the mitochondrial … WebGene ID: 100909697, discontinued on 16-Nov-2024. Summary. DISCONTINUED: This record was withdrawn by the Rat Genome Database (RGD). Other designations. mitochondrial … WebThe SLC25A24 gene provides instructions for producing a protein that is a member of the solute carrier (SLC) family of proteins. Proteins in the SLC family transport various compounds across the membranes surrounding the cell and its component parts. The protein produced from the SLC25A24 gene transports molecules across the inner … bishop thornton north yorkshire

SLC25A51 solute carrier family 25 member 51 [ (horse)]

SLC25A38 Gene - GeneCards S2538 Protein S2538 Antibody

WebWith 53 members, the mitochondrial carrier family (solute carrier family 25, SLC25) is the largest solute transporter family in humans. They transport solutes across the impermeable inner membrane of mitochondria for important cellular processes, such as oxidative phosphorylation of fats and sugars, amino acid catabolism and interconversion, synthesis … http://cucurbitgenomics.org/feature/gene/Carg02784 bishopthorpe parish council meeting minutesWebMay 9, 2014 · The human genome encodes 53 members of the solute carrier family 25 (SLC25), also called the mitochondrial carrier family, many of which have been shown to … bishopthorpe palace york postcode

"WebFor instance, the sodium- and chloride-de- 400 human solute carriers into 47 families.1 pendent neurotransmitter transporter family (SLC6) According to this classification, … " - Solute carrier family 25 member 51-like

Solute carrier family 25 member 51-like

The human gene SLC25A29, of solute carrier family 25, encodes a ...

WebAmong the DEG, there were five solute carriers: Solute carrier family 25 member 36 (SLC25A36), solute carrier family 37 member 1 (SLC37A1), solute carrier family 45 member 3 (SLC45A3), solute carrier family 52 member 3 (SLC52A3), and solute carrier family 6 member 20 (SLC6A20). WebGene ID: 100066182, updated on 16-Aug-2024. Summary Other designations. solute carrier family 25 member 51, mitochondrial carrier triple repeat protein-like protein, …

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WebApr 9, 2024 · The mitochondrial solute carrier SLC25A5 at Xq24 is a novel candidate gene for non-syndromic intellectual disability. Vandewalle J, et al. Hum Genet, 2013 Oct. PMID … Websolute carrier family 25 member 44: Location: Cucurbita_argyrosperma_scaffold_008 : 47135 .. 48181 (+) Genome Viewer Gene Expression Sequences The following sequences are available for this feature: Gene sequence (with intron) Legend: polypeptide exon CDS. Hold the cursor ...

WebJan 18, 2024 · Significant different expression was observed in voltage-gated ion channels (potassium voltage-gated channel subfamily A member 1, KCNA1; potassium voltage-gated channel subfamily C member 3, KCNC3; potassium two pore domain channel subfamily K member 1, KCNK1; sodium voltage-gated channel α subunit t9, SCN9A), transporters … WebOct 28, 2024 · The C-terminal half of aralar shares 28 to 29% identity with proteins of the mitochondrial solute carrier family, including oxoglutarate/malate carrier (604165), ADP/ATP translocase-2 (300150), UCP1 (113730), and tricarboxylate carrier (190315). Like the other mitochondrial carrier proteins, the C-terminal region of aralar contains 6 …

WebMay 22, 2024 · A variety of metabolites, nucleotides, and cofactors are transported across the inner mitochondrial membrane (IMM) by a superfamily of membrane transporters which are known as the mitochondrial carrier family (MCF) or the solute carrier family 25 (SLC25 protein family). In humans, the MCF has 53 members encoded by nuclear genes. WebMar 21, 2024 · GeneCards Summary for SLC25A38 Gene. SLC25A38 (Solute Carrier Family 25 Member 38) is a Protein Coding gene. Diseases associated with SLC25A38 include Anemia, Sideroblastic, 2, Pyridoxine-Refractory and Sideroblastic Anemia . An important paralog of this gene is SLC25A45.

WebMar 21, 2024 · GeneCards Summary for SLC25A38 Gene. SLC25A38 (Solute Carrier Family 25 Member 38) is a Protein Coding gene. Diseases associated with SLC25A38 include …

WebMar 29, 2024 · The protein encoded by this gene is a member of a transmembrane protein family that transports small molecules across membranes. The encoded protein has been found in lysosomal membranes, where it can transport catabolites from the lysosomes to the cytoplasm. This protein has been shown to be an effective transporter of the cytotoxic … bishopthorpe palace staffWebMay 18, 2010 · Solute carrier family 21 member 15; Gene names. Name. SLCO5A1. Synonyms. OATP5A1, SLC21A15. Organism names. Organism. ... 1.20.1250.20 MFS … bishopthorpe infant school yorkWebsolute carrier family 25 member 51b; solute carrier family 25 member 51-like; edit. Language Label Description Also known as; English: ... Protein found in Danio rerio. … bishopthorpe palace interiorWebFor instance, the sodium- and chloride-de- 400 human solute carriers into 47 families.1 pendent neurotransmitter transporter family (SLC6) According to this classification, members of a family consists of important neurosignaling proteins, such share a similar substrate and at least 20–25% as the dopamine and serotonin transporters.30,31 … bishopthorpe infant schoolWebSolute carrier family 25 (mitochondrial carrier; Graves disease autoantigen), member 16 is a protein in humans that is encoded by the SLC25A16 gene. This gene encodes a protein that contains three tandemly repeated mitochondrial carrier protein domains. bishopthorpe palace yorkWebSolute carrier family 39 (zinc transporter), member 14 (SLC39A14), is a member of the family of zinc transporters that functionally control intracellular zinc influx and efflux from intracellular compartments as well as between the extracellular and intracellular environment. 8 SLC39A14 encodes Zrt/IRT-like protein 14 (ZIP14), which is a zinc- and … bishopthorpe palace addressWebMay 7, 2024 · 610823 - SOLUTE CARRIER FAMILY 25, MEMBER 42; SLC25A42 - SLC25A42 In a 16-year-old boy, born of consanguineous Saudi parents, with recurrent metabolic crises with variable encephalomyopathic features and neurologic regression (MECREN; 618416), Shamseldin et al. (2016) identified a homozygous missense mutation in the SLC25A42 … dark souls scholar of the first sin g2a