Solute carrier family 15 member 4
WebJun 15, 2024 · In a 14-year-old Japanese girl with IPS, Tsuge et al. (2015) identified compound heterozygosity for novel missense mutations in the SLC27A4 gene ( 604194.0008, 604194.0009 ). The authors stated that this was the first report of a Japanese patient with IPS.
Solute carrier family 15 member 4
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WebLOC127866289 solute carrier family 15 member 4-like [] Gene ID: 127866289, updated on 7-Dec-2024. Summary Other designations. solute carrier ... WebFeb 2, 2024 · (a) Aligned structure of solute carrier family 4, sodium borate transporter, member 11 protein wildtype (891 aa, grey colour) and energy-minimised wildtype (cyan colour). ( b ) Aligned structure of SLC4A11 protein mutant type (grey colour) and energy-minimised mutant type (red colour).
WebDec 8, 2024 · NM_145648.4 → NP_663623.1 solute carrier family 15 member 4. See identical proteins and their annotated locations for NP_663623.1. Status: VALIDATED. … WebFeb 28, 2013 · Solute carrier family 15 member 4 (SLC15A4; PHT1) Download PDF. Download PDF. Published: 28 February 2013; Solute carrier family 15 member 4 …
WebOct 5, 2024 · SOLUTE CARRIER FAMILY 12 (POTASSIUM/CHLORIDE TRANSPORTER), ... In a French Canadian patient with ACCPN , Howard et al. (2002) found that 1 chromosome 15 allele carried the predominant French Canadian mutation ... In 4 affected members of a Japanese family (family 2) with axonal Charcot-Marie-Tooth disease type 2II (CMT2II ... WebDec 21, 2024 · 613350 - SOLUTE CARRIER FAMILY 52 (RIBOFLAVIN TRANSPORTER), ... In 3 affected members of a consanguineous Turkish family with Brown-Vialetto-Van Laere syndrome, ... Cassandra L. Kniffin - updated : 4/15/2010 Creation Date: ...
WebNov 8, 2024 · Predicted to be active in membrane. Is expressed in central nervous system and retina. Orthologous to human SLC45A4 (solute carrier family 45 member 4). [provided by Alliance of Genome Resources, Apr 2024] Expression Ubiquitous expression in adrenal adult (RPKM 15.9), ovary adult (RPKM 14.7) and 28 other tissues See more Orthologs …
WebMar 21, 2024 · SLC15A3 (Solute Carrier Family 15 Member 3) is a Protein Coding gene. Diseases associated with SLC15A3 include Hypotrichosis 4.Among its related pathways are Transport of inorganic cations/anions … siatech long beachWebThe 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 … sia techinfoWebAug 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 … siatech logoWebSolute 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 … siatech mycroschoolWebApr 1, 2016 · Innate immunity in shrimp is important in resisting bacterial infection. The NF-κB pathway is pivotal in such an immune response. This study cloned and functionally … sia technologies colombesWebsolute carrier family 15, member 4. Synonyms: PTR4, C130069N12Rik, PHT1. Order Alleles. ... All available products are supplied via our member's centres or partnerships. When … siatech californiaWebMonika 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 … the people harbour