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Details
Link-It Detail - Jax Mouse Phenotype - abnormal circulating creatinine level
Debug Stats
  • ### Total Build Time: 144 ms 19.943 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 402 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 276 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 183 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=2 ms Completed: 2 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=8 ms Completed: 8 ms rowSize= 592 bytes
  • CONCEPT_CHILDREN gt=7 ms Completed: 7 ms rowSize= 1.045 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.591 KB
  • CONCEPT_RELATIONSHIPS gt=2 ms Completed: 2 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=116 ms Completed: 116 ms rowSize= 14.569 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.175 KB
  • CONCEPT_ANCILLARY gt=2 ms Completed: 2 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal circulating creatinine level MP:0005328
Definition (1)
anomaly in the blood concentration of this product of creatine catabolism; abnormal levels indicative of renal dysfunction
Synonyms (1)
"abnormal creatinine level" EXACT
Parents (1)
img abnormal circulating amino acid level MP:0005311
Children (2)
img decreased circulating creatinine level MP:0005554
img increased circulating creatinine level MP:0005553
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053766img abnormal circulating amino acid level MP:0005311
Genes (80)

Species:
human : 80
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED
HumanNEK8284086NIMA-related kinase 8
INFERRED
HumanAQP11282679aquaporin 11
INFERRED
HumanCYS1192668cystin 1
INFERRED
HumanGLIS284662GLIS family zinc finger 2
INFERRED
HumanWDR8384292WD repeat domain 83
INFERRED
HumanUNC93B181622unc-93 homolog B1 (C. elegans)
INFERRED
HumanCOL18A180781collagen, type XVIII, alpha 1
INFERRED
HumanSLC4A557835solute carrier family 4 (sodium bicarbonate cotransporter), member 5
INFERRED
HumanC1GALT156913core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1
INFERRED
HumanSLC2A956606solute carrier family 2 (facilitated glucose transporter), member 9
INFERRED
HumanLGR455366leucine-rich repeat containing G protein-coupled receptor 4
INFERRED
HumanSLC47A155244solute carrier family 47 (multidrug and toxin extrusion), member 1
INFERRED
HumanRRM2B50484ribonucleotide reductase M2 B (TP53 inducible)
INFERRED
HumanTBK129110TANK-binding kinase 1
INFERRED
HumanGPSM126086G-protein signaling modulator 1
INFERRED
HumanCD2AP23607CD2-associated protein
INFERRED
HumanIKZF322806IKAROS family zinc finger 3 (Aiolos)
INFERRED
HumanCCNI10983cyclin I
INFERRED
HumanSLC34A210568solute carrier family 34 (type II sodium/phosphate contransporter), member 2
INFERRED
HumanMAFB9935v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog B
INFERRED
HumanIL27RA9466interleukin 27 receptor, alpha
INFERRED
HumanLARGE9215like-glycosyltransferase
INFERRED
HumanNPHS27827nephrosis 2, idiopathic, steroid-resistant (podocin)
INFERRED
HumanBSND7809Bartter syndrome, infantile, with sensorineural deafness (Barttin)
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0005328abnormal circulating creatinine level0self