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Details
Link-It Detail - Jax Mouse Phenotype - abnormal calcium ion homeostasis
Debug Stats
  • ### Total Build Time: 59 ms 21.616 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 392 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 312 bytes
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  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
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  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 579 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.496 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.578 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=52 ms Completed: 52 ms rowSize= 15.975 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.170 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal calcium ion homeostasis MP:0004231
Definition (1)
anomaly in the processes involved in the maintenance of an internal equilibrium of calcium ions within the body or between a cell and its external environment
Parents (1)
img abnormal ion homeostasis MP:0001765
Children (3)
img abnormal platelet calcium level MP:0004865
img abnormal renal calcium reabsorbtion MP:0010111
img abnormal circulating calcium level MP:0001562
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053765img abnormal ion homeostasis MP:0001765
Genes (75)

Species:
human : 75
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Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanCISD2493856CDGSH iron sulfur domain 2
Click here to display 48 evidence detail records.
HumanMPZL3196264myelin protein zero-like 3
INFERRED
HumanSLC34A3142680solute carrier family 34 (type II sodium/phosphate contransporter), member 3
INFERRED
HumanCATSPER1117144cation channel, sperm associated 1
Click here to display 48 evidence detail records.
HumanORAI184876ORAI calcium release-activated calcium modulator 1
INFERRED
HumanPLVAP83483plasmalemma vesicle associated protein
INFERRED
HumanFAM20C56975family with sequence similarity 20, member C
INFERRED
HumanTRPV556302transient receptor potential cation channel, subfamily V, member 5
Click here to display 48 evidence detail records.
HumanTRPV655503transient receptor potential cation channel, subfamily V, member 6
Click here to display 48 evidence detail records.
HumanBLOC1S455330biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino
INFERRED
HumanTMEM38B55151transmembrane protein 38B
Click here to display 48 evidence detail records.
HumanTRPM454795transient receptor potential cation channel, subfamily M, member 4
Click here to display 48 evidence detail records.
HumanWWOX51741WW domain containing oxidoreductase
INFERRED
HumanPLCE151196phospholipase C, epsilon 1
Click here to display 48 evidence detail records.
HumanSLC39A229986solute carrier family 39 (zinc transporter), member 2
Click here to display 48 evidence detail records.
HumanCLEC2D29121C-type lectin domain family 2, member D
INFERRED
HumanSLC24A225769solute carrier family 24 (sodium/potassium/calcium exchanger), member 2
Click here to display 48 evidence detail records.
HumanPLCL223228phospholipase C-like 2
Click here to display 48 evidence detail records.
HumanHSPA4L22824heat shock 70kDa protein 4-like
INFERRED
HumanRAPGEF411069Rap guanine nucleotide exchange factor (GEF) 4
Click here to display 48 evidence detail records.
HumanSLC26A110861solute carrier family 26 (anion exchanger), member 1
INFERRED
HumanCLDN1610686claudin 16
INFERRED
HumanSLC34A210568solute carrier family 34 (type II sodium/phosphate contransporter), member 2
INFERRED
HumanKL9365klotho
INFERRED
HumanCLDN109071claudin 10
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004231abnormal calcium ion homeostasis0self