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Details
Link-It Detail - Jax Mouse Phenotype - abnormal food intake
Debug Stats
  • ### Total Build Time: 337 ms 22.377 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 368 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 262 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 180 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=3 ms Completed: 3 ms rowSize= 579 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 2.339 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 1.577 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=324 ms Completed: 324 ms rowSize= 15.802 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.158 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal food intake MP:0005449
Definition (1)
any anomaly in the total number of calories/food amount taken in over time when compared to the normal state
Synonyms (1)
"abnormal energy intake" EXACT
Parents (1)
img abnormal eating behavior MP:0001431
Children (5)
img dysphagia MP:0003158
img aphagia MP:0001438
img abnormal saccharin consumption MP:0002849
img increased food intake MP:0011939
img decreased food intake MP:0011940
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053866img abnormal eating behavior MP:0001431
Genes (315)

Species:
human : 315
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMBOAT4619373membrane bound O-acyltransferase domain containing 4
INFERRED
HumanCISD2493856CDGSH iron sulfur domain 2
INFERRED
HumanBSX390259brain-specific homeobox
Click here to display 111 evidence detail records.
HumanNEGR1257194neuronal growth regulator 1
INFERRED
HumanLCLAT1253558lysocardiolipin acyltransferase 1
INFERRED
HumanRFX6222546regulatory factor X, 6
INFERRED
HumanCERS3204219ceramide synthase 3
INFERRED
HumanGSX2170825GS homeobox 2
INFERRED
HumanPHOSPHO1162466phosphatase, orphan 1
INFERRED
HumanKLB152831klotho beta
Click here to display 111 evidence detail records.
HumanCCDC80151887coiled-coil domain containing 80
Click here to display 111 evidence detail records.
HumanSLC30A7148867solute carrier family 30 (zinc transporter), member 7
INFERRED
HumanGSC145258goosecoid homeobox
INFERRED
HumanSLC32A1140679solute carrier family 32 (GABA vesicular transporter), member 1
Click here to display 111 evidence detail records.
HumanDMBX1127343diencephalon/mesencephalon homeobox 1
Click here to display 111 evidence detail records.
HumanCPT1C126129carnitine palmitoyltransferase 1C
INFERRED
HumanSLC25A25114789solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 25
INFERRED
HumanMOB1B92597MOB kinase activator 1B
INFERRED
HumanPKDCC91461protein kinase domain containing, cytoplasmic
INFERRED
HumanUCN290226urocortin 2
INFERRED
HumanGALP85569galanin-like peptide
INFERRED
HumanRSPO384870R-spondin 3
INFERRED
HumanACSS184532acyl-CoA synthetase short-chain family member 1
Click here to display 111 evidence detail records.
HumanARID5B84159AT rich interactive domain 5B (MRF1-like)
INFERRED
HumanRMI180010RecQ mediated genome instability 1
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0005449abnormal food intake0self