Vitamin D Deficiency Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

36 genes associated with the Vitamin D Deficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ADGRG5 adhesion G protein-coupled receptor G5
C10ORF88 chromosome 10 open reading frame 88
CASR calcium-sensing receptor
CYP24A1 cytochrome P450, family 24, subfamily A, polypeptide 1
CYP27A1 cytochrome P450, family 27, subfamily A, polypeptide 1
CYP27B1 cytochrome P450, family 27, subfamily B, polypeptide 1
CYP2R1 cytochrome P450, family 2, subfamily R, polypeptide 1
CYP3A4 cytochrome P450, family 3, subfamily A, polypeptide 4
DAB1 Dab, reelin signal transducer, homolog 1 (Drosophila)
DHCR7 7-dehydrocholesterol reductase
FCER1A Fc fragment of IgE, high affinity I, receptor for; alpha polypeptide
FCER1G Fc fragment of IgE, high affinity I, receptor for; gamma polypeptide
FLG filaggrin
GC group-specific component (vitamin D binding protein)
HERC2 HECT and RLD domain containing E3 ubiquitin protein ligase 2
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
IFNL3 interferon, lambda 3
IL13 interleukin 13
IL13RA1 interleukin 13 receptor, alpha 1
IL4 interleukin 4
IL4R interleukin 4 receptor
IRF4 interferon regulatory factor 4
KMT2C lysine (K)-specific methyltransferase 2C
LACC1 laccase (multicopper oxidoreductase) domain containing 1
MC1R melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor)
MCM6 minichromosome maintenance complex component 6
MED16 mediator complex subunit 16
MED24 mediator complex subunit 24
MS4A2 membrane-spanning 4-domains, subfamily A, member 2
NADSYN1 NAD synthetase 1
PLCB1 phospholipase C, beta 1 (phosphoinositide-specific)
PTH parathyroid hormone
RBFOX1 RNA binding protein, fox-1 homolog (C. elegans) 1
RXRG retinoid X receptor, gamma
TYRP1 tyrosinase-related protein 1
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor