Solute carrier family 25 member 51-like

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August undefined, 2024

WebFor 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 … WebDec 8, 2024 · Orthologous to human SLC25A13 (solute carrier family 25 member 13). [provided by Alliance of Genome Resources, Apr 2024] Expression Biased expression in liver E18 (RPKM 28.1), liver adult (RPKM 15.6) and 12 other tissues See more ... See all (51) citations in PubMed. GeneRIFs: ...

Solute carrier family 25 member 51b - Wikidata

WebSolute 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 … WebMay 31, 2024 · The solute carrier family 25 (SLC25) drives the import of a large diversity of metabolites into mitochondria, a key cellular structure involved in many metabolic functions. Mutations of the mitochondrial glutamate carrier SLC25A22 (also named GC1 ) have been identified in early epilepti … ravens wing branford

SLC25A46 Gene - GeneCards S2546 Protein S2546 Antibody

WebApr 10, 2024 · Selective macroautophagy/autophagy maintains cellular homeostasis through the lysosomal degradation of specific cellular proteins or organelles. The pro-survival effect of selective autophagy has been well-characterized, but the mechanism by which it drives cell death is still poorly understood. Here, we use a quantitative proteomic … WebMay 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 … WebSep 4, 2013 · ATG16 autophagy related 16-like 1: rs10210302: 2: SLC11A1: 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: ravenswing blackburn

84-1244-23 MCAR1, NT (SLC25A51, MCART1, Solute carrier family 25 member …

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

WebSolute carrier family 25 member 51 (Q21121355) From Wikidata. Jump to navigation Jump to search. mammalian protein found in Homo sapiens. mitochondrial carrier triple repeat … ravens wine glassesWebFeb 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, ... simpe editing want package

"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 SLC25 Mitochondrial Carrier Family: Structure and Mechanism

WebMar 21, 2024 · Complete information for SLC25A1P5 gene (Pseudogene), Solute Carrier Family 25 Member 1 Pseudogene 5, including: function, proteins, disorders, pathways, … WebJan 8, 2024 · Orthologous to several human genes including SLC25A51 (solute carrier family 25 member 51). [provided by Alliance of Genome Resources, Apr 2024] Slc25a51 …

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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 29, 2024 · SLC25A35 belongs to the SLC25 family of mitochondrial carrier proteins (Haitina et al., 2006 [PubMed 16949250]). [supplied by OMIM, Mar 2008] Expression. …

WebOct 27, 2024 · In a 9-year-old boy with mitochondrial DNA depletion syndrome-19 (MTDPS19; 618972 ), Punzi et al. (2024) identified compound heterozygous mutations in the SLC25A10 gene ( 606794.0001 and 606794.0002 ). The mutations were found by trio-based whole-exome sequencing and segregated with the disorder in the family. WebMar 29, 2024 · SLC25A4 solute carrier family 25 member 4 [ Homo sapiens (human) ] Gene ID: 291, updated on 29-Mar-2024. Download Datasets Summary. Go to the top of the page Help. Official ... HIV-1 Vpr peptides 27-51 and 71-82 …

WebJan 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 … 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 …

WebSLC25A22. Solute carrier family 25 member 22 is a protein that in humans is encoded by the SLC25A22 gene. This gene encodes a mitochondrial glutamate carrier. Mutations in …

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. ravens wing healing centerWebApr 14, 2024 · The pro-ferroptotic genes of Transferrin Receptor (TFR1), Solute Carrier Family 39 Member 14 (SLC39A14), Haem Oxygenase-1 (HMOX-1), Acyl-CoA Synthetase Long-chain Family Member 4 (ACSL4), Cyclooxygenase 2 (COX-2) and mitochondrial Voltage-dependent Anion Channels (VDACs) were up-regulated; the anti-ferroptotic … simpeg githubWebWith 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 … ravens wineryWebMay 18, 2010 · Solute carrier family 21 member 15; Gene names. Name. SLCO5A1. Synonyms. OATP5A1, SLC21A15. Organism names. Organism. ... 1.20.1250.20 MFS … simpegnew bnnWebApr 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 … ravenswing care home blackburnWebAug 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 … ravenswing cow parsleyWebMar 21, 2024 · GeneCards Summary for SLC25A38 Gene. SLC25A38 (Solute Carrier Family 25 Member 38) is a Protein Coding gene. Diseases associated with SLC25A38 include … ravenswing care home