Solute carrier family 25 member 51-like
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). 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 …
Solute carrier family 25 member 51-like
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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: 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 …
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. WebGene ID: 100909697, discontinued on 16-Nov-2024. Summary. DISCONTINUED: This record was withdrawn by the Rat Genome Database (RGD). Other designations. mitochondrial …
WebDescription: Homo sapiens solute carrier family 25 member 13 (SLC25A13), transcript variant 3, non-coding RNA. (from RefSeq NR_027662) RefSeq Summary (NM_014251): This gene is a member of the mitochondrial carrier family. The encoded protein contains four EF-hand Ca(2+) binding motifs in the N-terminal domain, and localizes to mitochondria. 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 …
WebMar 21, 2024 · GeneCards Summary for SLC25A46 Gene. SLC25A46 (Solute Carrier Family 25 Member 46) is a Protein Coding gene. Diseases associated with SLC25A46 include Pontocerebellar Hypoplasia, Type 1E and Neuropathy, Hereditary Motor And Sensory, Type Vib, With Optic Atrophy .
WebNov 7, 2024 · Welcome to the Family: Identification of the NAD + Transporter of Animal Mitochondria as Member of the Solute Carrier Family SLC25. Ziegler M, et al. … how is allergy skin test doneWebMar 21, 2024 · SLC25A35 belongs to the SLC25 family of mitochondrial carrier proteins (Haitina et al., 2006 [PubMed 16949250]).[supplied by OMIM, Mar 2008] GeneCards … high innate immunogenicityWebアズワンの【AXEL】84-1244-23 MCAR1, NT (SLC25A51, MCART1, Solute carrier family 25 member 51, Mitochondrial carrier triple repeat protein 1) 200ul 038261のコーナーです … high in music 3 crosswordWebMonika 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 … how is allotment done in hni categoryWebsolute 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. … how is a llc formedWebAug 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 … how is allergy testing done on kidsThe solute carrier (SLC) group of membrane transport proteins include over 400 members organized into 66 families. Most members of the SLC group are located in the cell membrane. The SLC gene nomenclature system was originally proposed by the HUGO Gene Nomenclature Committee (HGNC) and is the basis for the official HGNC names of the genes that encode these transporters. A more general transmembrane transporter classification can be found in TCDB da… high in marathi