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Details
Link-It Detail - Jax Mouse Phenotype - abnormal serotonin level
Debug Stats
  • ### Total Build Time: 222 ms 20.947 KB
  • CONCEPT_NAME gt=8 ms Completed: 8 ms rowSize= 376 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
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  • CONCEPT_PARENTS gt=12 ms Completed: 12 ms rowSize= 577 bytes
  • CONCEPT_CHILDREN gt=9 ms Completed: 9 ms rowSize= 1.479 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.576 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=186 ms Completed: 186 ms rowSize= 15.094 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.162 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal serotonin level MP:0005322
Definition (1)
anomaly in the amount of biochemical messenger and regulator, found in the CNS, gastrointestinal tract, and produced by platelets that mediates neurotransmission, gastrointestinal motility, hemostasis, and cardiovascular integrity
Synonyms (1)
"abnormal hydroxytryptamine level" EXACT
Parents (1)
img abnormal hormone level MP:0003953
Children (3)
img abnormal platelet serotonin level MP:0004723
img increased serotonin level MP:0010069
img decreased serotonin level MP:0010070
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053765img abnormal hormone level MP:0003953
Genes (59)

Species:
human : 59
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSLC35D3340146solute carrier family 35, member D3
INFERRED
HumanTAAR1134864trace amine associated receptor 1
INFERRED
HumanTPH2121278tryptophan hydroxylase 2
Click here to display 65 evidence detail records.
HumanFOXP293986forkhead box P2
Click here to display 65 evidence detail records.
HumanHPS384343Hermansky-Pudlak syndrome 3
INFERRED
HumanDTNBP184062dystrobrevin binding protein 1
INFERRED
HumanBLOC1S563915biogenesis of lysosomal organelles complex-1, subunit 5, muted
INFERRED
HumanCELF660677CUGBP, Elav-like family member 6
INFERRED
HumanBLOC1S455330biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino
INFERRED
HumanFEV54738FEV (ETS oncogene family)
INFERRED
HumanDISC127185disrupted in schizophrenia 1
INFERRED
HumanBLOC1S626258biogenesis of lysosomal organelles complex-1, subunit 6, pallidin
INFERRED
HumanSLC7A1123657solute carrier family 7 (anionic amino acid transporter light chain, xc- system), member 11
INFERRED
HumanLPHN323284latrophilin 3
INFERRED
HumanMFN29927mitofusin 2
INFERRED
HumanGTF2IRD19569GTF2I repeat domain containing 1
Click here to display 65 evidence detail records.
HumanMAGED19500melanoma antigen family D, 1
Click here to display 65 evidence detail records.
HumanAP3D18943adaptor-related protein complex 3, delta 1 subunit
INFERRED
HumanAP3B18546adaptor-related protein complex 3, beta 1 subunit
INFERRED
HumanZNF1487707zinc finger protein 148
INFERRED
HumanUBE3A7337ubiquitin protein ligase E3A
INFERRED
HumanTPH17166tryptophan hydroxylase 1
Click here to display 65 evidence detail records.
HumanTNF7124tumor necrosis factor
Click here to display 65 evidence detail records.
HumanTH7054tyrosine hydroxylase
Click here to display 65 evidence detail records.
HumanTDO26999tryptophan 2,3-dioxygenase
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0005322abnormal serotonin level0self