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Table 3 NBD risk genes identified in GWAS

From: Emerging genetic complexity and rare genetic variants in neurodegenerative brain diseases

NBD

Risk genes

References

AD

ABCA7, ACE, ADAM10, ADAMTS1, APOE, BIN1, BCKDK, CASS4, CD2AP, CD33, CELF1, CLU, CR1, DSG2, EPHA1, FERMT2, HLA-DRB1, HLA-DRB5, INPP5D, IQCK, KAT8CR1, MEF2C, MS4A6A, NME8, PICALM, PTK2B, SLC24A4, SORL1, WWOX, ZCWPW1

[24,25,26,27,28,29,30]

PD

ACMSD, ASXL3, BCKDK, BRIP1, BST1, C5orf24, CAB39L, CCDC62, CD19, CHRNB1, CLCN3, CRLS1, DDRGK1, DGKQ, DNAH17, DYRK1A, FAM171A2, FAM47E, FAM49B, FBRSL1, FCGR2A, FGF20, FYN, GAK, GBA, GBF1, GPNMB, HIP1, HLA-DQB1, HLA-DRA, HLA-DRB5, INPP5F, KCNIP3, KCNS3, KPNA1, LAMP, LCORL, LINC00693, MAPT, MBNL2, MCCC1/3, MED12L, MEX3C, MIPOL1, NOD2, NUCKS, PAM, RAB29, RAB7L1, RAI1, RIMS1, RIT2, RNF141, RPS12, RPS6KL1, SCAF11, SCARB2, SIPA1L2, SNCA, SPTSSB, SREBF1, STBD1, STK39,STX1B, SYT11, TMEM163, TMEM175, TRIM40, UBAP2, UBTF, VAMP4, VPS13C

[22, 31,32,33]

FTD

BTNL2, C4orf27, CTSC, DPP6, HLA-DRA, HLA-DRB5, HLA-DQA2, IMMP2L, IRF2, MIR548AP, OLFM1, RAB38, RERG, TMEM106B, UNC13A

[21, 34]

ALS

C21orf2, DPP6, FGGY, ITPR2, KIF5A, MOBP, SARM, SCFD1, UNC13A

[23, 35, 36]