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Details
Link-It Detail - Jax Mouse Phenotype - absent spleen
Debug Stats
  • ### Total Build Time: 103 ms 14.672 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 354 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 240 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 175 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=11 ms Completed: 11 ms rowSize= 581 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=10 ms Completed: 10 ms rowSize= 2.915 KB
  • CONCEPT_RELATIONSHIPS gt=2 ms Completed: 2 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=68 ms Completed: 68 ms rowSize= 9.135 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.151 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
absent spleen MP:0000690
Definition (1)
missing organ that functions to filter blood and to store red corpuscles and platelets
Synonyms (1)
"absence of spleen" EXACT
Parents (1)
img abnormal spleen morphology MP:0000689
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img immune system phenotype MP:00053876img abnormal spleen morphology MP:0000689
img mammalian phenotype MP:0000001img hematopoietic system phenotype MP:00053975img abnormal spleen morphology MP:0000689
Genes (15)

Species:
human : 15
SpeciesGeneGeneIdGene NameEvidence
HumanCFC1B653275cripto, FRL-1, cryptic family 1B
Click here to display 31 evidence detail records.
HumanNKX2-3159296
Click here to display 31 evidence detail records.
HumanCFC155997cripto, FRL-1, cryptic family 1
Click here to display 31 evidence detail records.
HumanMKS154903Meckel syndrome, type 1
Click here to display 31 evidence detail records.
HumanFOXN18456forkhead box N1
Click here to display 31 evidence detail records.
HumanKAT6A7994K(lysine) acetyltransferase 6A
Click here to display 31 evidence detail records.
HumanWT17490Wilms tumor 1
Click here to display 31 evidence detail records.
HumanTCF216943transcription factor 21
Click here to display 31 evidence detail records.
HumanSOX116664SRY (sex determining region Y)-box 11
Click here to display 31 evidence detail records.
HumanPKD25311polycystic kidney disease 2 (autosomal dominant)
Click here to display 31 evidence detail records.
HumanTLX13195T-cell leukemia homeobox 1
Click here to display 31 evidence detail records.
HumanELAVL11994ELAV (embryonic lethal, abnormal vision, Drosophila)-like 1 (Hu antigen R)
Click here to display 31 evidence detail records.
HumanMEGF81954multiple EGF-like-domains 8
Click here to display 31 evidence detail records.
HumanDNAH51767dynein, axonemal, heavy chain 5
Click here to display 31 evidence detail records.
HumanNKX3-2579
Click here to display 31 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000690absent spleen0self