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Details
Link-It Detail - Jax Mouse Phenotype - decreased salivation
Debug Stats
  • ### Total Build Time: 19 ms 15.861 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 368 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 207 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 170 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 589 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 567 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.941 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=18 ms Completed: 18 ms rowSize= 9.761 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.158 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
decreased salivation MP:0000623
Definition (1)
reduction in the flow, secretion, or amount of saliva
Synonyms (1)
"sialoschesis" EXACT
Parents (1)
img abnormal salivary gland physiology MP:0005310
Children (1)
img xerostomia MP:0000624
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img endocrine/exocrine gland phenotype MP:00053795img abnormal salivary gland physiology MP:0005310
img mammalian phenotype MP:0000001img digestive/alimentary phenotype MP:00053815img abnormal salivary gland physiology MP:0005310
Genes (16)

Species:
human : 16
SpeciesGeneGeneIdGene NameEvidence
HumanTRAF3IP210758TRAF3 interacting protein 2
INFERRED
HumanTRPC17220transient receptor potential cation channel, subfamily C, member 1
Click here to display 26 evidence detail records.
HumanST146768suppression of tumorigenicity 14 (colon carcinoma)
Click here to display 26 evidence detail records.
HumanSLC12A26558solute carrier family 12 (sodium/potassium/chloride transporter), member 2
Click here to display 26 evidence detail records.
HumanSLC9A16548solute carrier family 9, subfamily A (NHE1, cation proton antiporter 1), member 1
Click here to display 26 evidence detail records.
HumanOPRK14986opioid receptor, kappa 1
Click here to display 26 evidence detail records.
HumanNKX3-14824
Click here to display 26 evidence detail records.
HumanITPR33710inositol 1,4,5-trisphosphate receptor, type 3
Click here to display 26 evidence detail records.
HumanID33399inhibitor of DNA binding 3, dominant negative helix-loop-helix protein
Click here to display 26 evidence detail records.
HumanE2F11869E2F transcription factor 1
Click here to display 26 evidence detail records.
HumanCHRM51133cholinergic receptor, muscarinic 5
Click here to display 26 evidence detail records.
HumanCHRM31131cholinergic receptor, muscarinic 3
Click here to display 26 evidence detail records.
HumanCHRM11128cholinergic receptor, muscarinic 1
Click here to display 26 evidence detail records.
HumanBBS4585Bardet-Biedl syndrome 4
Click here to display 26 evidence detail records.
HumanBBS2583Bardet-Biedl syndrome 2
Click here to display 26 evidence detail records.
HumanAQP5362aquaporin 5
Click here to display 26 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000623decreased salivation0self