15q13 3 copy number variation syndrome Gene Set

Dataset WikiPathways Pathways 2024
Category structural or functional annotations
Type pathway
External Link https://www.wikipathways.org/pathways/WP4942.html
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Genes

20 proteins participating in the 15q13 3 copy number variation syndrome pathway from the WikiPathways Pathways 2024 dataset.

Symbol Name
ARHGAP11B Rho GTPase activating protein 11B
CCL5 chemokine (C-C motif) ligand 5
CHRFAM7A CHRNA7 (cholinergic receptor, nicotinic, alpha 7, exons 5-10) and FAM7A (family with sequence similarity 7A, exons A-E) fusion
CHRNA7 cholinergic receptor, nicotinic, alpha 7 (neuronal)
CREBBP CREB binding protein
FAN1 FANCD2/FANCI-associated nuclease 1
FANCD2 Fanconi anemia, complementation group D2
FYN FYN proto-oncogene, Src family tyrosine kinase
GOLGA8H golgin A8 family, member H
GOLGA8O golgin A8 family, member O
GOLGA8Q golgin A8 family, member Q
GOLGA8R golgin A8 family, member R
GPR75 G protein-coupled receptor 75
GRM6 glutamate receptor, metabotropic 6
KAT2B K(lysine) acetyltransferase 2B
KLF13 Kruppel-like factor 13
MTMR10 myotubularin related protein 10
OTUD7A OTU deubiquitinase 7A
SERPINH1 serpin peptidase inhibitor, clade H (heat shock protein 47), member 1, (collagen binding protein 1)
TRPM1 transient receptor potential cation channel, subfamily M, member 1