decreased circulating creatinine level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description less than the normal blood concentration of this product of creatine catabolism; abnormal levels indicative of renal dysfunction (Mammalian Phenotype Ontology, MP_0005554)
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33 gene mutations causing the decreased circulating creatinine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADORA3 adenosine A3 receptor
BSND barttin CLCNK-type chloride channel accessory beta subunit
CCR2 chemokine (C-C motif) receptor 2
CD44 CD44 molecule (Indian blood group)
CISD2 CDGSH iron sulfur domain 2
CTH cystathionine gamma-lyase
CXCR3 chemokine (C-X-C motif) receptor 3
DNASE1 deoxyribonuclease I
GPR107 G protein-coupled receptor 107
IL10 interleukin 10
IL1R1 interleukin 1 receptor, type I
MARCH9 membrane-associated ring finger (C3HC4) 9
MEP1B meprin A, beta
MYO10 myosin X
MYO7A myosin VIIA
PARP1 poly (ADP-ribose) polymerase 1
PHYKPL 5-phosphohydroxy-L-lysine phospho-lyase
PRKCZ protein kinase C, zeta
RNASE10 ribonuclease, RNase A family, 10 (non-active)
RNF10 ring finger protein 10
SELK selenoprotein K
SETMAR SET domain and mariner transposase fusion gene
SLC12A1 solute carrier family 12 (sodium/potassium/chloride transporter), member 1
SLC34A2 solute carrier family 34 (type II sodium/phosphate cotransporter), member 2
SLC4A5 solute carrier family 4 (sodium bicarbonate cotransporter), member 5
SLC52A2 solute carrier family 52 (riboflavin transporter), member 2
SMAD3 SMAD family member 3
SYK spleen tyrosine kinase
TNFRSF1B tumor necrosis factor receptor superfamily, member 1B
USP21 ubiquitin specific peptidase 21
USP38 ubiquitin specific peptidase 38
WDR83 WD repeat domain 83
WTAP Wilms tumor 1 associated protein