apolipoproteins b Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description disease cluster belonging to disease group metabolic (Genetic Association Database)
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Genes

26 genes associated with the disease apolipoproteins b in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
C2CD5 C2 calcium-dependent domain containing 5
CCBE1 collagen and calcium binding EGF domains 1
DNAJC13 DnaJ (Hsp40) homolog, subfamily C, member 13
EFNB2 ephrin-B2
EPHA4 EPH receptor A4
FRMPD4 FERM and PDZ domain containing 4
HP haptoglobin
HPR haptoglobin-related protein
KLHL14 kelch-like family member 14
LRP1B low density lipoprotein receptor-related protein 1B
MGAT4C MGAT4 family, member C
MYO16 myosin XVI
PDE1C phosphodiesterase 1C, calmodulin-dependent 70kDa
PDE4D phosphodiesterase 4D, cAMP-specific
PLA2R1 phospholipase A2 receptor 1, 180kDa
PLCB1 phospholipase C, beta 1 (phosphoinositide-specific)
PTPRK protein tyrosine phosphatase, receptor type, K
RBFOX1 RNA binding protein, fox-1 homolog (C. elegans) 1
SH3GL2 SH3-domain GRB2-like 2
SLC25A26 solute carrier family 25 (S-adenosylmethionine carrier), member 26
SLC41A2 solute carrier family 41 (magnesium transporter), member 2
STIM1 stromal interaction molecule 1
TRIM44 tripartite motif containing 44
TRMT11 tRNA methyltransferase 11 homolog (S. cerevisiae)
TRPM3 transient receptor potential cation channel, subfamily M, member 3
TSPAN5 tetraspanin 5