lat2 Gene Set

Dataset GeneRIF Biological Term Annotations
Category structural or functional annotations
Type biological term
Description linker for activation of T cells family, member 2|This gene is one of the contiguous genes at 7q11.23 commonly deleted in Williams syndrome, a multisystem developmental disorder. This gene consists of at least 14 exons, and its alternative splicing generates 3 transcript variants, all encoding the same protein. [provided by RefSeq, Jul 2008] (NCBI Entrez Gene Database, 7462)
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Genes

11 genes co-occuring with the biological term lat2 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Symbol Name
LAT2 linker for activation of T cells family, member 2
RUNX1 runt-related transcription factor 1
RUNX1T1 runt-related transcription factor 1; translocated to, 1 (cyclin D-related)
SLC16A10 solute carrier family 16 (aromatic amino acid transporter), member 10
SLC3A2 solute carrier family 3 (amino acid transporter heavy chain), member 2
SLC7A5 solute carrier family 7 (amino acid transporter light chain, L system), member 5
SLC7A8 solute carrier family 7 (amino acid transporter light chain, L system), member 8
SLCO1A2 solute carrier organic anion transporter family, member 1A2
SLCO1C1 solute carrier organic anion transporter family, member 1C1
SLCO3A1 solute carrier organic anion transporter family, member 3A1
SLCO4A1 solute carrier organic anion transporter family, member 4A1