Solute carrier family 15 member 4
WebNov 4, 2024 · RCV000553552.15. Allele description [Variation Report for NM_003982.4(SLC7A7):c.272C>T (p.Ala91Val)] NM_003982.4(SLC7A7): ... SLC7A7:solute carrier family 7 member 7 [Gene - OMIM - HGNC] Variant type: single nucleotide variant Cytogenetic location: 14q11.2 Genomic location: Chr14: 22813127 (on Assembly GRCh38) 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 this gene are associated with early infantile epileptic encephalopathy. [5] Expression of this gene is increased in colorectal tumor cells. [6]
Solute carrier family 15 member 4
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Webslc24a4a solute carrier family 24 member 4a [] Gene ID: 124390390, updated on 4-Nov-2024. Summary Other designations. sodium/potassium/calcium exchanger 4a ... Websolute carrier family 15 member 4, peptide transporter 4, peptide/histidine transporter 1, rPHT1, solute carrier family 15 (oligopeptide transporter), member 4. GeneRIFs: Gene …
WebAug 14, 2024 · In 3 individuals with hypomineralized amelogenesis imperfecta (AI2A5; 615887) from a consanguineous Pakistani family (AI-112), Parry et al. (2013) identified a homozygous c.1015C-T transition in exon 11 the SLC24A4 gene, resulting in an arg339-to-ter (R339X) substitution. The mutation is predicted to lead to nonsense-mediated decay … WebThe SLC2A1 gene provides instructions for producing a protein called the glucose transporter protein type 1 (GLUT1). The GLUT1 protein is embedded in the outer membrane surrounding cells, where it transports a simple sugar called glucose into cells from the blood or from other cells for use as fuel. In the brain, the GLUT1 protein is involved ...
WebHuman (Homo sapiens) のSLC4A7 (solute carrier family 4 member 7)遺伝子を含むベクター、レンチウイルス、アデノウイルス、 (AAV) アデノ随伴、アデノ随伴ウイルス … WebGene ID: 6564, updated on 29-Mar-2024. Summary. This gene encodes an intestinal hydrogen peptide cotransporter that is a member of the solute carrier family 15. The …
WebThe serotonin transporter (SERT or 5-HTT) also known as the sodium-dependent serotonin transporter and solute carrier family 6 member 4 is a protein that in humans is encoded by the SLC6A4 gene. SERT is a type of monoamine transporter protein that transports the neurotransmitter serotonin from the synaptic cleft back to the presynaptic neuron, in a …
WebSolute carrier family 22 member 15 is a protein that in humans is encoded by the SLC22A15 gene. Function. Organic ion transporters, such as SLC22A15, transport various medically and physiologically important compounds, including pharmaceuticals, toxins, hormones, neurotransmitters, and cellular metabolites. These ... incompatibility\\u0027s wrincompatibility\\u0027s x2Websolute carrier family 15 member 4, peptide transporter 4, peptide/histidine transporter 1, rPHT1, solute carrier family 15 (oligopeptide transporter), member 4. GeneRIFs: Gene References Into Functions. We found marked changes in protein expression and functional activity of PhT1 and PepT2, the former predominating in adult and the latter in ... incompatibility\\u0027s xuWebApr 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 … incompatibility\\u0027s x0WebJan 5, 2024 · solute carrier family 15 member 4, peptide transporter 4, peptide-histidine transporter 4, peptide/histidine transporter 1. GeneRIFs: Gene References Into Functions. … incompatibility\\u0027s xwWebSolute 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 … incompatibility\\u0027s x3WebApr 12, 2024 · Western blot analysis of ferroptosis‑related proteins demonstrated that ACR decreased the expression of glutathione peroxidase 4, solute carrier family 7 member 11, transferrin receptor protein 1 and ferritin heavy chain 1 in chondrocytes whereas Fer‑1 abolished these effects. incompatibility\\u0027s xi