abnormal vitamin homeostasis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the processes involved in the maintenance of an internal equilibrium of organic substances found in food and are not synthesized by the body and are necessary in trace amounts for normal metabolic function (Mammalian Phenotype Ontology, MP_0004019)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004019
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Genes

47 gene mutations causing the abnormal vitamin homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCA1 ATP-binding cassette, sub-family A (ABC1), member 1
ABCA4 ATP-binding cassette, sub-family A (ABC1), member 4
ABCB4 ATP-binding cassette, sub-family B (MDR/TAP), member 4
ADH7 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide
AKR1A1 aldo-keto reductase family 1, member A1 (aldehyde reductase)
AKR1B1 aldo-keto reductase family 1, member B1 (aldose reductase)
BCO1 beta-carotene oxygenase 1
CD320 CD320 molecule
CLDN16 claudin 16
CYP24A1 cytochrome P450, family 24, subfamily A, polypeptide 1
CYP27A1 cytochrome P450, family 27, subfamily A, polypeptide 1
CYP7A1 cytochrome P450, family 7, subfamily A, polypeptide 1
DGAT1 diacylglycerol O-acyltransferase 1
FGF23 fibroblast growth factor 23
FOLR1 folate receptor 1 (adult)
GALNT3 polypeptide N-acetylgalactosaminyltransferase 3
GC group-specific component (vitamin D binding protein)
KCP kielin/chordin-like protein
KL klotho
LASP1 LIM and SH3 protein 1
LRAT lecithin retinol acyltransferase (phosphatidylcholine--retinol O-acyltransferase)
MTHFD1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1, methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthetase
MTHFS 5,10-methenyltetrahydrofolate synthetase (5-formyltetrahydrofolate cyclo-ligase)
PHEX phosphate regulating endopeptidase homolog, X-linked
PITPNA phosphatidylinositol transfer protein, alpha
PLTP phospholipid transfer protein
RARG retinoic acid receptor, gamma
RBP1 retinol binding protein 1, cellular
RBP2 retinol binding protein 2, cellular
RBP4 retinol binding protein 4, plasma
RBP7 retinol binding protein 7, cellular
RDH16 retinol dehydrogenase 16 (all-trans)
RGN regucalcin
RHO rhodopsin
SIK3 SIK family kinase 3
SLC19A3 solute carrier family 19 (thiamine transporter), member 3
SLC23A1 solute carrier family 23 (ascorbic acid transporter), member 1
SLC23A2 solute carrier family 23 (ascorbic acid transporter), member 2
SLC34A1 solute carrier family 34 (type II sodium/phosphate cotransporter), member 1
SLC34A2 solute carrier family 34 (type II sodium/phosphate cotransporter), member 2
SLC34A3 solute carrier family 34 (type II sodium/phosphate cotransporter), member 3
STRA6 stimulated by retinoic acid 6
TGIF1 TGFB-induced factor homeobox 1
TRPV5 transient receptor potential cation channel, subfamily V, member 5
TTPA tocopherol (alpha) transfer protein
TTR transthyretin
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor