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Details
Link-It Detail - Jax Mouse Phenotype - abnormal susceptibility to weight gain
Debug Stats
  • ### Total Build Time: 39 ms 20.832 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 404 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 287 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=0 Completed: 0 ms rowSize= 575 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 1.047 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.563 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=31 ms Completed: 31 ms rowSize= 15.665 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.176 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal susceptibility to weight gain MP:0011117
Definition (1)
anomaly in body weight over time when compared to the average increase in weight on the same diet, with equal energy (calorie) intake
Parents (1)
img abnormal body weight MP:0001259
Children (2)
img decreased susceptibility to weight gain MP:0010182
img increased susceptibility to weight gain MP:0005455
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img growth/size phenotype MP:00053786img abnormal body weight MP:0001259
Genes (185)

Species:
human : 185
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMBOAT4619373membrane bound O-acyltransferase domain containing 4
INFERRED
HumanFFAR4338557free fatty acid receptor 4
INFERRED
HumanSLC13A5284111solute carrier family 13 (sodium-dependent citrate transporter), member 5
img Jax MP, Pubmed Id: 21803289, MOUSE PHENOTYPE ID: MGI:3037150
HumanLCLAT1253558lysocardiolipin acyltransferase 1
INFERRED
HumanRICTOR253260RPTOR independent companion of MTOR, complex 2
INFERRED
HumanPIKFYVE200576phosphoinositide kinase, FYVE finger containing
INFERRED
HumanSLC30A8169026solute carrier family 30 (zinc transporter), member 8
INFERRED
HumanSGMS2166929sphingomyelin synthase 2
INFERRED
HumanBBS12166379Bardet-Biedl syndrome 12
INFERRED
HumanKLB152831klotho beta
INFERRED
HumanCCDC80151887coiled-coil domain containing 80
INFERRED
HumanGPBAR1151306G protein-coupled bile acid receptor 1
INFERRED
HumanSLC32A1140679solute carrier family 32 (GABA vesicular transporter), member 1
INFERRED
HumanCPT1C126129carnitine palmitoyltransferase 1C
INFERRED
HumanRLN3117579relaxin 3
INFERRED
HumanOMA1115209OMA1 zinc metallopeptidase
INFERRED
HumanSLC25A25114789solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 25
INFERRED
HumanTP53INP194241tumor protein p53 inducible nuclear protein 1
INFERRED
HumanGALP85569galanin-like peptide
INFERRED
HumanMFSD2A84879major facilitator superfamily domain containing 2A
INFERRED
HumanARID5B84159AT rich interactive domain 5B (MRF1-like)
INFERRED
HumanMOGAT280168monoacylglycerol O-acyltransferase 2
INFERRED
HumanRMI180010RecQ mediated genome instability 1
INFERRED
HumanADIPOR279602adiponectin receptor 2
INFERRED
HumanFTO79068fat mass and obesity associated
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0011117abnormal susceptibility to weight gain0self