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Details
Link-It Detail - Jax Mouse Phenotype - abnormal Kupffer cell morphology
Debug Stats
  • ### Total Build Time: 51 ms 25.435 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 392 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 263 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 181 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=3 ms Completed: 3 ms rowSize= 1.031 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=26 ms Completed: 26 ms rowSize= 12.362 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=17 ms Completed: 17 ms rowSize= 9.902 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.170 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal Kupffer cell morphology MP:0008114
Definition (1)
any structural anomaly of the phagocytic macrophages residing on the luminal surface of the hepatic sinusoids
Synonyms (1)
"abnormal Kupffer's cell" EXACT
Parents (2)
img abnormal macrophage morphology MP:0002446
img abnormal liver sinusoid morphology MP:0008989
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img immune system phenotype MP:00053877img abnormal macrophage morphology MP:0002446
img mammalian phenotype MP:0000001img hematopoietic system phenotype MP:00053979img abnormal macrophage morphology MP:0002446
img mammalian phenotype MP:0000001img immune system phenotype MP:00053879img abnormal macrophage morphology MP:0002446
img mammalian phenotype MP:0000001img hematopoietic system phenotype MP:000539710img abnormal macrophage morphology MP:0002446
img mammalian phenotype MP:0000001img immune system phenotype MP:000538710img abnormal macrophage morphology MP:0002446
img mammalian phenotype MP:0000001img hematopoietic system phenotype MP:000539711img abnormal macrophage morphology MP:0002446
img mammalian phenotype MP:0000001img liver/biliary system phenotype MP:00053708img abnormal liver sinusoid morphology MP:0008989
img mammalian phenotype MP:0000001img liver/biliary system phenotype MP:00053707img abnormal liver sinusoid morphology MP:0008989
img mammalian phenotype MP:0000001img cardiovascular system phenotype MP:00053857img abnormal liver sinusoid morphology MP:0008989
Genes (16)

Species:
human : 16
SpeciesGeneGeneIdGene NameEvidence
HumanUACA55075uveal autoantigen with coiled-coil domains and ankyrin repeats
Click here to display 19 evidence detail records.
HumanZDHHC1354503zinc finger, DHHC-type containing 13
Click here to display 19 evidence detail records.
HumanRFX55993regulatory factor X, 5 (influences HLA class II expression)
Click here to display 19 evidence detail records.
HumanPRKAG15571protein kinase, AMP-activated, gamma 1 non-catalytic subunit
Click here to display 19 evidence detail records.
HumanNGFR4804nerve growth factor receptor
Click here to display 19 evidence detail records.
HumanNEU14758sialidase 1 (lysosomal sialidase)
Click here to display 19 evidence detail records.
HumanNAGLU4669N-acetylglucosaminidase, alpha
Click here to display 19 evidence detail records.
HumanMANBA4126mannosidase, beta A, lysosomal
Click here to display 19 evidence detail records.
HumanMAN2B14125mannosidase, alpha, class 2B, member 1
Click here to display 19 evidence detail records.
HumanLIPA3988lipase A, lysosomal acid, cholesterol esterase
Click here to display 19 evidence detail records.
HumanCTBS1486chitobiase, di-N-acetyl-
Click here to display 19 evidence detail records.
HumanCSF11435colony stimulating factor 1 (macrophage)
Click here to display 19 evidence detail records.
HumanCP1356ceruloplasmin (ferroxidase)
Click here to display 19 evidence detail records.
HumanCCR51234chemokine (C-C motif) receptor 5 (gene/pseudogene)
Click here to display 19 evidence detail records.
HumanCCR11230chemokine (C-C motif) receptor 1
Click here to display 19 evidence detail records.
HumanENTPD5957ectonucleoside triphosphate diphosphohydrolase 5
Click here to display 19 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0008114abnormal Kupffer cell morphology0self