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Details
Link-It Detail - Jax Mouse Phenotype - abnormal glucose homeostasis
Debug Stats
  • ### Total Build Time: 2,275 ms 26.457 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 384 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 270 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 186 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= 575 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 6.034 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.574 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=2,268 ms Completed: 2.268 Seconds rowSize= 16.156 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.166 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal glucose homeostasis MP:0002078
Definition (1)
anomaly in the processes involved in the maintenance of an internal equilibrium of glucose in the fluids and tissues
Synonyms (1)
"abnormal glucose metabolism" NARROW
Parents (1)
img abnormal homeostasis MP:0001764
Children (13)
img abnormal glucagon secretion MP:0003565
img abnormal glucose tolerance MP:0005291
img abnormal insulin clearance MP:0003839
img abnormal insulin secretion MP:0003564
img abnormal glycogen homeostasis MP:0005438
img increased insulin sensitivity MP:0002891
img abnormal gluconeogenesis MP:0003383
img abnormal circulating glucose level MP:0000188
img abnormal circulating glucagon level MP:0002695
img abnormal urine glucose level MP:0001758
img abnormal circulating insulin level MP:0001560
img insulin resistance MP:0005331
img abnormal renal glucose reabsorption MP:0011447
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053764img abnormal homeostasis MP:0001764
Genes (600)

Species:
human : 600
Page Size
Current 25
  Page 1 of 24
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMBOAT4619373membrane bound O-acyltransferase domain containing 4
INFERRED
HumanCISD2493856CDGSH iron sulfur domain 2
Click here to display 398 evidence detail records.
HumanMAFA389692v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog A
INFERRED
HumanILDR2387597immunoglobulin-like domain containing receptor 2
INFERRED
HumanNHLRC1378884NHL repeat containing 1
INFERRED
HumanSLC27A1376497solute carrier family 27 (fatty acid transporter), member 1
Click here to display 398 evidence detail records.
HumanSLC6A19340024solute carrier family 6 (neutral amino acid transporter), member 19
INFERRED
HumanFFAR4338557free fatty acid receptor 4
INFERRED
HumanPTRF284119polymerase I and transcript release factor
INFERRED
HumanSLC13A5284111solute carrier family 13 (sodium-dependent citrate transporter), member 5
Click here to display 398 evidence detail records.
HumanSGMS1259230sphingomyelin synthase 1
INFERRED
HumanPTF1A256297pancreas specific transcription factor, 1a
INFERRED
HumanLCLAT1253558lysocardiolipin acyltransferase 1
INFERRED
HumanRICTOR253260RPTOR independent companion of MTOR, complex 2
Click here to display 398 evidence detail records.
HumanGPRC6A222545G protein-coupled receptor, family C, group 6, member A
Click here to display 398 evidence detail records.
HumanPIKFYVE200576phosphoinositide kinase, FYVE finger containing
INFERRED
HumanCRTC2200186CREB regulated transcription coactivator 2
Click here to display 398 evidence detail records.
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
INFERRED
HumanARX170302aristaless related homeobox
INFERRED
HumanGLIS3169792GLIS family zinc finger 3
INFERRED
HumanSLC30A8169026solute carrier family 30 (zinc transporter), member 8
INFERRED
HumanSGMS2166929sphingomyelin synthase 2
INFERRED
HumanBBS12166379Bardet-Biedl syndrome 12
INFERRED
HumanKLB152831klotho beta
Click here to display 398 evidence detail records.
HumanCCDC80151887coiled-coil domain containing 80
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0002078abnormal glucose homeostasis0self