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Details
Link-It Detail - Jax Mouse Phenotype - abnormal spleen iron level
Debug Stats
  • ### Total Build Time: 75 ms 23.188 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 380 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 212 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 184 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=14 ms Completed: 14 ms rowSize= 1.013 KB
  • CONCEPT_CHILDREN gt=12 ms Completed: 12 ms rowSize= 1.023 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 4.255 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=39 ms Completed: 39 ms rowSize= 14.830 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.164 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal spleen iron level MP:0008739
Definition (1)
anomaly in the amount of iron present in the spleen tissue
Synonyms (1)
"abnormal splenic iron load" EXACT
Parents (2)
img abnormal iron level MP:0001770
img abnormal spleen morphology MP:0000689
Children (2)
img decreased spleen iron level MP:0008808
img increased spleen iron level MP:0008809
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053767img abnormal iron level MP:0001770
img mammalian phenotype MP:0000001img hematopoietic system phenotype MP:00053975img abnormal spleen morphology MP:0000689
img mammalian phenotype MP:0000001img immune system phenotype MP:00053876img abnormal spleen morphology MP:0000689
Genes (26)

Species:
human : 26
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanTMPRSS6164656transmembrane protease, serine 6
img Jax MP, Pubmed Id: 22490684, MOUSE PHENOTYPE ID: MGI:1919003
HumanHFE2148738hemochromatosis type 2 (juvenile)
INFERRED
HumanSPIC121599Spi-C transcription factor (Spi-1/PU.1 related)
INFERRED
HumanANKH56172ANKH inorganic pyrophosphate transport regulator
INFERRED
HumanEXOC654536exocyst complex component 6
INFERRED
HumanSLC40A130061solute carrier family 40 (iron-regulated transporter), member 1
INFERRED
HumanFBXL526234F-box and leucine-rich repeat protein 5
INFERRED
HumanHYAL28692hyaluronoglucosaminidase 2
INFERRED
HumanUROS7390uroporphyrinogen III synthase
INFERRED
HumanTFRC7037transferrin receptor (p90, CD71)
INFERRED
HumanTFR27036transferrin receptor 2
INFERRED
HumanSPTA16708spectrin, alpha, erythrocytic 1 (elliptocytosis 2)
INFERRED
HumanPRKAG15571protein kinase, AMP-activated, gamma 1 non-catalytic subunit
INFERRED
HumanSLC11A24891solute carrier family 11 (proton-coupled divalent metal ion transporter), member 2
INFERRED
HumanMEOX24223mesenchyme homeobox 2
INFERRED
HumanLTF4057lactotransferrin
INFERRED
HumanKCNN43783potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4
INFERRED
HumanIREB23658iron-responsive element binding protein 2
INFERRED
HumanIL103586interleukin 10
INFERRED
HumanHFE3077hemochromatosis
INFERRED
HumanHBB3043hemoglobin, beta
INFERRED
HumanEPB422038erythrocyte membrane protein band 4.2
INFERRED
HumanEPB412035erythrocyte membrane protein band 4.1 (elliptocytosis 1, RH-linked)
INFERRED
HumanCP1356ceruloplasmin (ferroxidase)
INFERRED
HumanANK1286ankyrin 1, erythrocytic
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0008739abnormal spleen iron level0self