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Details
Link-It Detail - Jax Mouse Phenotype - abnormal consumption behavior
Debug Stats
  • ### Total Build Time: 79 ms 20.374 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 386 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 248 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 209 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= 572 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 1.020 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.570 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=77 ms Completed: 77 ms rowSize= 15.091 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.167 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal consumption behavior MP:0002069
Definition (1)
altered ability or inability to eat or drink, or unusual choice or avoidance of foods or drink
Synonyms (1)
"neurological/behavioral: feeding/drinking anomalies" EXACT
Parents (1)
img abnormal behavior MP:0004924
Children (2)
img abnormal drinking behavior MP:0001422
img abnormal eating behavior MP:0001431
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img behavior/neurological phenotype MP:00053864img abnormal behavior MP:0004924
Genes (502)

Species:
human : 502
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCCR2729230chemokine (C-C motif) receptor 2
INFERRED
HumanMBOAT4619373membrane bound O-acyltransferase domain containing 4
INFERRED
HumanCISD2493856CDGSH iron sulfur domain 2
INFERRED
HumanEIF2AK4440275eukaryotic translation initiation factor 2 alpha kinase 4
INFERRED
HumanCCL3L3414062chemokine (C-C motif) ligand 3-like 3
INFERRED
HumanHELT391723helt bHLH transcription factor
INFERRED
HumanBSX390259brain-specific homeobox
INFERRED
HumanNEGR1257194neuronal growth regulator 1
INFERRED
HumanLCLAT1253558lysocardiolipin acyltransferase 1
INFERRED
HumanRFX6222546regulatory factor X, 6
INFERRED
HumanCERS3204219ceramide synthase 3
INFERRED
HumanCYS1192668cystin 1
INFERRED
HumanGSX2170825GS homeobox 2
INFERRED
HumanBBS12166379Bardet-Biedl syndrome 12
INFERRED
HumanPHOSPHO1162466phosphatase, orphan 1
INFERRED
HumanKLB152831klotho beta
INFERRED
HumanCCDC80151887coiled-coil domain containing 80
INFERRED
HumanSLC30A7148867solute carrier family 30 (zinc transporter), member 7
INFERRED
HumanGSC145258goosecoid homeobox
INFERRED
HumanSLC32A1140679solute carrier family 32 (GABA vesicular transporter), member 1
INFERRED
HumanUBR3130507ubiquitin protein ligase E3 component n-recognin 3 (putative)
INFERRED
HumanDMBX1127343diencephalon/mesencephalon homeobox 1
INFERRED
HumanCPT1C126129carnitine palmitoyltransferase 1C
INFERRED
HumanTPH2121278tryptophan hydroxylase 2
INFERRED
HumanSLC25A25114789solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 25
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0002069abnormal consumption behavior0self