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Details
Link-It Detail - Jax Mouse Phenotype - abnormal urination
Debug Stats
  • ### Total Build Time: 91 ms 23.598 KB
  • CONCEPT_NAME gt=9 ms Completed: 9 ms rowSize= 364 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 304 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 178 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
  • CONCEPT_NAMESPACE gt=NONE 1 ms Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=6 ms Completed: 6 ms rowSize= 595 bytes
  • CONCEPT_CHILDREN gt=14 ms Completed: 14 ms rowSize= 4.092 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.592 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=51 ms Completed: 51 ms rowSize= 15.206 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.156 KB
  • CONCEPT_ANCILLARY gt=2 ms Completed: 2 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal urination MP:0001756
Definition (1)
anomaly in the process in which parasympathetic nerves stimulate the bladder wall muscle to contract resulting in the expulsion of urine from the body
Synonyms (1)
"abnormal micturition" EXACT
Parents (1)
img abnormal renal/urinary system physiology MP:0005502
Children (9)
img decreased urine flow rate MP:0011432
img urinary incontinence MP:0003280
img anuria MP:0003624
img polyuria MP:0001762
img ischuria MP:0003622
img dysuria MP:0003621
img abnormal urination pattern MP:0001761
img oliguria MP:0003620
img increased urine flow rate MP:0011431
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img renal/urinary system phenotype MP:00053674img abnormal renal/urinary system physiology MP:0005502
Genes (119)

Species:
human : 119
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCISD2493856CDGSH iron sulfur domain 2
INFERRED
HumanOIT3170392oncoprotein induced transcript 3
INFERRED
HumanSLC26A7115111solute carrier family 26 (anion exchanger), member 7
INFERRED
HumanWNT3A89780wingless-type MMTV integration site family, member 3A
Click here to display 7 evidence detail records.
HumanGLIS284662GLIS family zinc finger 2
INFERRED
HumanSLC4A1183959solute carrier family 4, sodium borate transporter, member 11
INFERRED
HumanWNK465266WNK lysine deficient protein kinase 4
INFERRED
HumanWNK165125WNK lysine deficient protein kinase 1
INFERRED
HumanTRPV459341transient receptor potential cation channel, subfamily V, member 4
INFERRED
HumanSLC4A557835solute carrier family 4 (sodium bicarbonate cotransporter), member 5
INFERRED
HumanTMEM2757393transmembrane protein 27
INFERRED
HumanAGTRAP57085angiotensin II receptor-associated protein
INFERRED
HumanSLC2A956606solute carrier family 2 (facilitated glucose transporter), member 9
INFERRED
HumanTRPV556302transient receptor potential cation channel, subfamily V, member 5
INFERRED
HumanTRPV655503transient receptor potential cation channel, subfamily V, member 6
INFERRED
HumanPI4K2A55361phosphatidylinositol 4-kinase type 2 alpha
INFERRED
HumanLIN7C55327lin-7 homolog C (C. elegans)
INFERRED
HumanFXYD453828FXYD domain containing ion transport regulator 4
INFERRED
HumanATP6V0A450617ATPase, H+ transporting, lysosomal V0 subunit a4
INFERRED
HumanTFCP2L129842transcription factor CP2-like 1
INFERRED
HumanWWTR125937WW domain containing transcription regulator 1
INFERRED
HumanNEDD4L23327neural precursor cell expressed, developmentally down-regulated 4-like, E3 ubiquitin protein ligase
INFERRED
HumanDKK122943dickkopf WNT signaling pathway inhibitor 1
INFERRED
HumanSIX210736SIX homeobox 2
INFERRED
HumanVAV310451vav 3 guanine nucleotide exchange factor
Click here to display 7 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001756abnormal urination0self