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WormBase Tree Display for Gene: HGNC:11066

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Name Class

HGNC:11066IdentityNameCGC_nameSlc7a8Inferred_automaticallyAGR_import
Other_nameRGD:1345085
L-type amino acid transporter 2
Lat2
LPI-PC1
hLAT2
integral membrane protein E16H
large neutral amino acids transporter small subunit 2
solute carrier family 7 (amino acid transporter light chain, L system), member 8
solute carrier family 7 (amino acid transporter, L-type), member 8
solute carrier family 7 (cationic amino acid transporter, y+ system), member 8
Public_nameSlc7a8
DB_infoDatabaseHGNCid11066
AGRcURIHGNC:11066
EnsEMBLENSEMBL_geneIDENSG00000092068
UniProtUniProt_ACQ9UHI5
SpeciesHomo sapiens
StatusLive
Gene_infoBiotypeSO:0001217
OrthologWBGene00000002Caenorhabditis elegansFrom_analysisEnsEMBL-Compara
Inparanoid
OMA
OrthoFinder
OrthoInspector
Panther
SonicParanoid
WBGene00000004Caenorhabditis elegansFrom_analysisInparanoid
OMA
OrthoFinder
OrthoInspector
Panther
SonicParanoid
WBGene00000003Caenorhabditis elegansFrom_analysisEnsEMBL-Compara
OMA
Panther
Structured_descriptionAutomated_descriptionEnables several functions, including neutral amino acid transmembrane transporter activity; thyroid hormone transmembrane transporter activity; and toxin transmembrane transporter activity. Involved in L-alanine import across plasma membrane; L-leucine import across plasma membrane; and thyroid hormone transport. Located in plasma membrane. Part of basolateral plasma membrane and microvillus membrane. [provided by Alliance of Genome Resources, Apr 2022]Inferred_automaticallyAGR_import