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Details
Link-It Detail - Jax Mouse Phenotype - abnormal fluid intake
Debug Stats
  • ### Total Build Time: 37 ms 21.026 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 370 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 255 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=6 ms Completed: 6 ms rowSize= 581 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.014 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.579 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=22 ms Completed: 22 ms rowSize= 15.952 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.159 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal fluid intake MP:0011947
Definition (1)
significant anomaly in the total amount of fluid taken in over time when compared to the normal state
Parents (1)
img abnormal drinking behavior MP:0001422
Children (2)
img decreased fluid intake MP:0011942
img increased fluid intake MP:0011941
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053866img abnormal drinking behavior MP:0001422
Genes (95)

Species:
human : 95
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED
HumanCISD2493856CDGSH iron sulfur domain 2
INFERRED
HumanCCL3L3414062chemokine (C-C motif) ligand 3-like 3
INFERRED
HumanLCLAT1253558lysocardiolipin acyltransferase 1
INFERRED
HumanPHOSPHO1162466phosphatase, orphan 1
INFERRED
HumanGLIS284662GLIS family zinc finger 2
INFERRED
HumanTRPV459341transient receptor potential cation channel, subfamily V, member 4
INFERRED
HumanMARK457787MAP/microtubule affinity-regulating kinase 4
INFERRED
HumanUNC7957578unc-79 homolog (C. elegans)
INFERRED
HumanPDSS257107prenyl (decaprenyl) diphosphate synthase, subunit 2
INFERRED
HumanSLC2A956606solute carrier family 2 (facilitated glucose transporter), member 9
INFERRED
HumanTRPV556302transient receptor potential cation channel, subfamily V, member 5
INFERRED
HumanHIF1AN55662hypoxia inducible factor 1, alpha subunit inhibitor
INFERRED
HumanFXYD453828FXYD domain containing ion transport regulator 4
INFERRED
HumanATP6V0A450617ATPase, H+ transporting, lysosomal V0 subunit a4
INFERRED
HumanTRIB228951tribbles homolog 2 (Drosophila)
INFERRED
HumanSIRT123411sirtuin 1
INFERRED
HumanNEDD4L23327neural precursor cell expressed, developmentally down-regulated 4-like, E3 ubiquitin protein ligase
INFERRED
HumanPROKR110887prokineticin receptor 1
img Jax MP, Pubmed Id: 16793879, MOUSE PHENOTYPE ID: MGI:1929676
img Jax MP, Pubmed Id: 7477266, MOUSE PHENOTYPE ID: MGI:87966
HumanAGPAT2105551-acylglycerol-3-phosphate O-acyltransferase 2
INFERRED
HumanMTSS19788metastasis suppressor 1
INFERRED
HumanCLDN109071claudin 10
INFERRED
HumanVAMP88673vesicle-associated membrane protein 8
INFERRED
HumanIRS28660insulin receptor substrate 2
INFERRED
HumanUNC5C8633unc-5 homolog C (C. elegans)
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0011947abnormal fluid intake0self