abnormal renal filtration rate Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description altered ability of the kidneys to remove substances from the plasma for excretion in a specific period of time (Mammalian Phenotype Ontology, MP_0005556)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005556
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Genes

25 gene mutations causing the abnormal renal filtration rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADCY6 adenylate cyclase 6
ADM adrenomedullin
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
AGXT alanine-glyoxylate aminotransferase
APRT adenine phosphoribosyltransferase
ARHGDIA Rho GDP dissociation inhibitor (GDI) alpha
ASL argininosuccinate lyase
BRAF B-Raf proto-oncogene, serine/threonine kinase
CRIM1 cysteine rich transmembrane BMP regulator 1 (chordin-like)
GUCA2B guanylate cyclase activator 2B (uroguanylin)
HNF1A HNF1 homeobox A
HP haptoglobin
KCNK5 potassium channel, two pore domain subfamily K, member 5
LEPR leptin receptor
LIN7C lin-7 homolog C (C. elegans)
MAS1 MAS1 proto-oncogene, G protein-coupled receptor
PIK3C2A phosphatidylinositol-4-phosphate 3-kinase, catalytic subunit type 2 alpha
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1
SLC14A1 solute carrier family 14 (urea transporter), member 1 (Kidd blood group)
SLC23A1 solute carrier family 23 (ascorbic acid transporter), member 1
SLC4A1 solute carrier family 4 (anion exchanger), member 1 (Diego blood group)
SLC5A2 solute carrier family 5 (sodium/glucose cotransporter), member 2
UMOD uromodulin
VAV2 vav 2 guanine nucleotide exchange factor
VAV3 vav 3 guanine nucleotide exchange factor