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Details
Link-It Detail - Jax Mouse Phenotype - abnormal spleen marginal zone morphology
Debug Stats
  • ### Total Build Time: 61 ms 22.462 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 408 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 377 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 199 bytes
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  • CONCEPT_SEMANTIC_TYPE gt=0 Completed: 0 ms rowSize= 14 bytes
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  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 592 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.514 KB
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  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=52 ms Completed: 52 ms rowSize= 15.150 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.178 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal spleen marginal zone morphology MP:0002362
Definition (1)
any structural anomaly of the zone between the red and white pulp of the spleen containing numerous macrophages and lymphocytes, and a rich plexus of sinusoids supplied by white pulp arterioles carrying blood-borne antigens
Synonyms (1)
"abnormal splenic marginal zone morphology" EXACT
Parents (1)
img abnormal spleen white pulp morphology MP:0002357
Children (3)
img abnormal spleen marginal zone macrophage morphology MP:0008240
img absent spleen marginal zone MP:0008234
img abnormal marginal zone B cell morphology MP:0008180
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img immune system phenotype MP:00053877img abnormal spleen white pulp morphology MP:0002357
img mammalian phenotype MP:0000001img hematopoietic system phenotype MP:00053976img abnormal spleen white pulp morphology MP:0002357
Genes (118)

Species:
human : 118
Page Size
Current 25
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SpeciesGeneGeneIdGene NameEvidence
HumanATP11C286410ATPase, class VI, type 11C
INFERRED
HumanGAPT202309GRB2-binding adaptor protein, transmembrane
INFERRED
HumanGIMAP1170575GTPase, IMAP family member 1
INFERRED
HumanNKX2-3159296
INFERRED
HumanTNFRSF13C115650tumor necrosis factor receptor superfamily, member 13C
INFERRED
HumanSPPL2A84888signal peptide peptidase like 2A
INFERRED
HumanNFKBID84807nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, delta
INFERRED
HumanB3GNT584002UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5
INFERRED
HumanSHARPIN81858SHANK-associated RH domain interactor
INFERRED
HumanDOCK881704dedicator of cytokinesis 8
INFERRED
HumanUNC93B181622unc-93 homolog B1 (C. elegans)
INFERRED
HumanACKR357007atypical chemokine receptor 3
INFERRED
HumanPCID255795PCI domain containing 2
INFERRED
HumanSASH354440SAM and SH3 domain containing 3
INFERRED
HumanSIAE54414sialic acid acetylesterase
INFERRED
HumanTLR851311toll-like receptor 8
Click here to display 45 evidence detail records.
HumanTLR751284toll-like receptor 7
Click here to display 45 evidence detail records.
HumanFOXP350943forkhead box P3
INFERRED
HumanBLNK29760B-cell linker
INFERRED
HumanDLL128514delta-like 1 (Drosophila)
INFERRED
HumanTNFRSF13B23495tumor necrosis factor receptor superfamily, member 13B
INFERRED
HumanSPEN23013spen homolog, transcriptional regulator (Drosophila)
INFERRED
HumanIKZF322806IKAROS family zinc finger 3 (Aiolos)
Click here to display 45 evidence detail records.
HumanRRAS222800related RAS viral (r-ras) oncogene homolog 2
INFERRED
HumanTREX111277three prime repair exonuclease 1
Click here to display 45 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0002362abnormal spleen marginal zone morphology0self