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Details
Link-It Detail - Jax Mouse Phenotype - abnormal liver parenchyma morphology
Debug Stats
  • ### Total Build Time: 29 ms 20.722 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 400 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 235 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 196 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= 580 bytes
  • CONCEPT_CHILDREN gt=6 ms Completed: 6 ms rowSize= 1.034 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.577 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=19 ms Completed: 19 ms rowSize= 15.414 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.174 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal liver parenchyma morphology MP:0008986
Definition (1)
any structural anomaly of the functional units of the liver including the lobules
Synonyms (1)
"abnormal hepatic parenchyma morphology" EXACT
Parents (1)
img abnormal liver morphology MP:0000598
Children (2)
img abnormal portal lobule morphology MP:0008992
img abnormal liver lobule morphology MP:0008987
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img liver/biliary system phenotype MP:00053705img abnormal liver morphology MP:0000598
Genes (162)

Species:
human : 162
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanGIMAP1-GIMAP5100527949
Click here to display 13 evidence detail records.
HumanSLC13A5284111solute carrier family 13 (sodium-dependent citrate transporter), member 5
INFERRED
HumanAQP11282679aquaporin 11
INFERRED
HumanRDH10157506retinol dehydrogenase 10 (all-trans)
Click here to display 13 evidence detail records.
HumanHFE2148738hemochromatosis type 2 (juvenile)
INFERRED
HumanTWIST2117581twist basic helix-loop-helix transcription factor 2
INFERRED
HumanTHEM4117145thioesterase superfamily member 4
INFERRED
HumanCTHRC1115908collagen triple helix repeat containing 1
INFERRED
HumanBICC180114bicaudal C homolog 1 (Drosophila)
Click here to display 13 evidence detail records.
HumanSAV160485salvador homolog 1 (Drosophila)
INFERRED
HumanPCTP58488phosphatidylcholine transfer protein
INFERRED
HumanGPAM57678glycerol-3-phosphate acyltransferase, mitochondrial
INFERRED
HumanRPTOR57521regulatory associated protein of MTOR, complex 1
INFERRED
HumanBIRC657448baculoviral IAP repeat containing 6
INFERRED
HumanTTC7A57217tetratricopeptide repeat domain 7A
INFERRED
HumanPNPLA257104patatin-like phospholipase domain containing 2
INFERRED
HumanBIN355909bridging integrator 3
INFERRED
HumanHR55806hair growth associated
INFERRED
HumanUACA55075uveal autoantigen with coiled-coil domains and ankyrin repeats
INFERRED
HumanPHIP55023pleckstrin homology domain interacting protein
INFERRED
HumanZDHHC1354503zinc finger, DHHC-type containing 13
INFERRED
HumanAZIN151582antizyme inhibitor 1
Click here to display 13 evidence detail records.
HumanVPS5451542vacuolar protein sorting 54 homolog (S. cerevisiae)
INFERRED
HumanGOLM151280golgi membrane protein 1
INFERRED
HumanFOXP350943forkhead box P3
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0008986abnormal liver parenchyma morphology0self