alkaline phosphatase Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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23 genes associated with the disease alkaline phosphatase in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ABCB11 ATP-binding cassette, sub-family B (MDR/TAP), member 11
ABHD12 abhydrolase domain containing 12
ABO ABO blood group (transferase A, alpha 1-3-N-acetylgalactosaminyltransferase; transferase B, alpha 1-3-galactosyltransferase)
ADAMTS13 ADAM metallopeptidase with thrombospondin type 1 motif, 13
C12ORF43 chromosome 12 open reading frame 43
CACFD1 calcium channel flower domain containing 1
CLEC9A C-type lectin domain family 9, member A
CNGA3 cyclic nucleotide gated channel alpha 3
FADS2 fatty acid desaturase 2
FAM13A family with sequence similarity 13, member A
FUT2 fucosyltransferase 2 (secretor status included)
GCNT2 glucosaminyl (N-acetyl) transferase 2, I-branching enzyme (I blood group)
GGT1 gamma-glutamyltransferase 1
GPLD1 glycosylphosphatidylinositol specific phospholipase D1
JMJD1C jumonji domain containing 1C
LRRC75B leucine rich repeat containing 75B
NBPF3 neuroblastoma breakpoint family, member 3
PDZRN4 PDZ domain containing ring finger 4
PNPLA3 patatin-like phospholipase domain containing 3
SEMA5A sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A
ST3GAL4 ST3 beta-galactoside alpha-2,3-sialyltransferase 4
ST8SIA6 ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 6
UNC13C unc-13 homolog C (C. elegans)