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Details
Link-It Detail - Jax Mouse Phenotype - abnormal circulating glucose level
Debug Stats
  • ### Total Build Time: 129 ms 22.611 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 396 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 239 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=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=5 ms Completed: 5 ms rowSize= 1.021 KB
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.039 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.928 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=115 ms Completed: 115 ms rowSize= 15.505 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.172 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal circulating glucose level MP:0000188
Definition (1)
any anomaly in the concentration in the blood of the major monosaccharide of the body
Synonyms (1)
"abnormal blood glucose level" EXACT
Parents (2)
img abnormal blood homeostasis MP:0009642
img abnormal glucose homeostasis MP:0002078
Children (2)
img increased circulating glucose level MP:0005559
img decreased circulating glucose level MP:0005560
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053765img abnormal blood homeostasis MP:0009642
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053765img abnormal glucose homeostasis MP:0002078
Genes (394)

Species:
human : 394
Page Size
Current 25
  Page 1 of 16
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanMBOAT4619373membrane bound O-acyltransferase domain containing 4
INFERRED
HumanMAFA389692v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog A
INFERRED
HumanILDR2387597immunoglobulin-like domain containing receptor 2
INFERRED
HumanFFAR4338557free fatty acid receptor 4
INFERRED
HumanSLC13A5284111solute carrier family 13 (sodium-dependent citrate transporter), member 5
INFERRED
HumanSGMS1259230sphingomyelin synthase 1
INFERRED
HumanPTF1A256297pancreas specific transcription factor, 1a
INFERRED
HumanLCLAT1253558lysocardiolipin acyltransferase 1
INFERRED
HumanRICTOR253260RPTOR independent companion of MTOR, complex 2
INFERRED
HumanGPRC6A222545G protein-coupled receptor, family C, group 6, member A
INFERRED
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
Click here to display 53 evidence detail records.
HumanBBS12166379Bardet-Biedl syndrome 12
INFERRED
HumanKLB152831klotho beta
Click here to display 53 evidence detail records.
HumanCCDC80151887coiled-coil domain containing 80
INFERRED
HumanPPM1L151742protein phosphatase, Mg2+/Mn2+ dependent, 1L
INFERRED
HumanCPT1C126129carnitine palmitoyltransferase 1C
INFERRED
HumanTWIST2117581twist basic helix-loop-helix transcription factor 2
INFERRED
HumanAGAP2116986ArfGAP with GTPase domain, ankyrin repeat and PH domain 2
INFERRED
HumanCTHRC1115908collagen triple helix repeat containing 1
INFERRED
HumanSYTL494121synaptotagmin-like 4
INFERRED
HumanPPP1R15B84919protein phosphatase 1, regulatory subunit 15B
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000188abnormal circulating glucose level0self