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15 records found for search term Slc38a8
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RGD IDSymbolNameDescriptionChrStartStopSpeciesAnnotationsMatchType
1560237Slc38a8solute carrier family 38, member 8ENCODES a protein that exhibits monoatomic cation transmembrane transporter activity (inferred); neutral L-amino acid transmembrane transporter activity (inferred); secondary active transmembrane transporter activity (inferred); INVOLVED IN aspartate metabolic process (ortholog); neuron projection d196443252464468852Rat57symbol , PhenoGengene, protein-coding, VALIDATED [RefSeq]
1618141Slc38a8solute carrier family 38, member 8Predicted to enable L-amino acid transmembrane transporter activity. Acts upstream of or within several processes, including aspartate metabolic process; nervous system development; and retinal pigment epithelium development. Predicted to be located in axon and cell cortex. Predicted to be active in8120206313120228503Mouse66symbol , old_gene_name , PhenoGen , descriptiongene, protein-coding, VALIDATED [RefSeq]
2290191SLC38A8solute carrier family 38 member 8This gene encodes a putative sodium-dependent amino-acid/proton antiporter. The protein has eleven transmembrane domains, an extracellular N-terminus and an intracellular C-terminal tail. The protein is a member of the SLC38 sodium-coupled neutral amino acid transporter family of proteins. Mutations168400966784043372Human87symbol , old_gene_name , COSMIC , Human Proteome Mapgene, protein-coding, REVIEWED [RefSeq]
8994392Slc38a8solute carrier family 38 member 8INVOLVED IN aspartate metabolic process (ortholog); neuron projection development (ortholog); optic nerve development (ortholog); ASSOCIATED WITH Foveal Hypoplasia (ortholog); foveal hypoplasia 2 (ortholog); genetic disease (ortholog)NW_004955564233796252565Chinchilla13symbolgene, protein-coding, MODEL [RefSeq]
11942769SLC38A8solute carrier family 38 member 8ENCODES a protein that exhibits L-amino acid transmembrane transporter activity (inferred); INVOLVED IN aspartate metabolic process (ortholog); neuron projection development (ortholog); optic nerve development (ortholog); ASSOCIATED WITH Foveal Hypoplasia (ortholog); foveal hypoplasia 2 (ortholog); 166467678764709083Bonobo20symbolgene, protein-coding, MODEL [RefSeq]
12208408SLC38A8solute carrier family 38 member 8INVOLVED IN aspartate metabolic process (ortholog); neuron projection development (ortholog); optic nerve development (ortholog); ASSOCIATED WITH Foveal Hypoplasia (ortholog); foveal hypoplasia 2 (ortholog); genetic disease (ortholog); FOUND IN membrane (inferred)56828986468308381Dog19symbolgene, protein-coding, MODEL [RefSeq]
12615999Slc38a8solute carrier family 38 member 8ENCODES a protein that exhibits L-amino acid transmembrane transporter activity (inferred); INVOLVED IN aspartate metabolic process (ortholog); neuron projection development (ortholog); optic nerve development (ortholog); ASSOCIATED WITH Foveal Hypoplasia (ortholog); foveal hypoplasia 2 (ortholog); NW_00493664137571073778939Squirrel19symbolgene, protein-coding, MODEL [RefSeq]
155248292slc38a8Tropical Clawed Frogsymbolgene, null
14033050SLC38A8solute carrier family 38 member 8INVOLVED IN aspartate metabolic process (ortholog); neuron projection development (ortholog); optic nerve development (ortholog); ASSOCIATED WITH Foveal Hypoplasia (ortholog); foveal hypoplasia 2 (ortholog); genetic disease (ortholog); FOUND IN membrane (inferred)Pig19symbolgene, protein-coding, MODEL [RefSeq]
18779678SLC38A8solute carrier family 38 member 8INVOLVED IN aspartate metabolic process (ortholog); neuron projection development (ortholog); optic nerve development (ortholog); ASSOCIATED WITH Foveal Hypoplasia (ortholog); foveal hypoplasia 2 (ortholog); genetic disease (ortholog)Green Monkey13symbolgene, protein-coding, MODEL [RefSeq]
18904904Slc38a8solute carrier family 38 member 8ENCODES a protein that exhibits L-amino acid transmembrane transporter activity (inferred); INVOLVED IN aspartate metabolic process (ortholog); neuron projection development (ortholog); optic nerve development (ortholog); ASSOCIATED WITH Foveal Hypoplasia (ortholog); foveal hypoplasia 2 (ortholog); Naked Mole-Rat19symbolgene, protein-coding, MODEL [RefSeq]
625865627Slc38a8solute carrier family 38 member 8INVOLVED IN aspartate metabolic process (ortholog); neuron projection development (ortholog); optic nerve development (ortholog); ASSOCIATED WITH Foveal Hypoplasia (ortholog); foveal hypoplasia 2 (ortholog); genetic disease (ortholog)Black Rat13symbolgene, protein-coding, MODEL [RefSeq]
20865934SLC38A8solute carrier family 38 member 8ENCODES a protein that exhibits L-amino acid transmembrane transporter activity (inferred); INVOLVED IN amino acid transmembrane transport (inferred); L-alpha-amino acid transmembrane transport (inferred); FOUND IN membrane (inferred)Green Monkey5symbolgene, protein-coding
155248291slc38a8.LAfrican Clawed Frogsymbolgene, null
16570975AC040169.4novel transcript, antisense to SLC38A8Humannamegene, lncrna