Logo arc image image
GATACA
  • Pin/Unpin Search
  • Pin/Unpin Details
Status:
Global Actions
Concepts: 0 (0)   Selected: 0 (0
Clear All Selections
 
Search
Text Search Results
Text Search Query:
none
Text Search Options:
none

Guided Help

Text Search Results
GraphTree Minimize or Maximize this Category
 Disease: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Anatomy: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Gene: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Jax Mouse Phenotype: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Human Phenotype: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Biological Processes: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Cellular Component: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Gene Ontology: Molecular Function: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Pathway: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 Drug: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Genomic Expression Atlas --
      Microarray Datasets: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 PubMed: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
GraphTree Minimize or Maximize this Category
 CoExpression Atlas: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 CoExpression: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Minimize or Maximize this Category
 Interactions: 0
No results.
 Concepts (w/Genes): 0 (0)   Selected (w/genes): 0 (0)
Details
Link-It Detail - Jax Mouse Phenotype - abnormal circulating mineral level
Debug Stats
  • ### Total Build Time: 263 ms 25.131 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 396 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 383 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 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=0 Completed: 0 ms rowSize= 1.016 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 3.801 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.922 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=241 ms Completed: 241 ms rowSize= 15.315 KB
  • CONCEPT_XREFS gt=22 ms Completed: 22 ms rowSize= 1.172 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal circulating mineral level MP:0006357
Definition (1)
any anomaly in the concentration in the blood of any naturally occurring, homogeneous inorganic solid substance having a definite chemical composition and highly ordered atomic arrangement that is required for growth and survival
Parents (2)
img abnormal mineral level MP:0000192
img abnormal blood homeostasis MP:0009642
Children (8)
img abnormal circulating copper level MP:0006348
img abnormal circulating potassium level MP:0002668
img abnormal circulating magnesium level MP:0001771
img abnormal circulating sulfate level MP:0002851
img abnormal circulating calcium level MP:0001562
img abnormal circulating iron level MP:0004152
img abnormal circulating phosphate level MP:0001565
img abnormal circulating sodium level MP:0001776
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053766img abnormal mineral level MP:0000192
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053765img abnormal blood homeostasis MP:0009642
Genes (137)

Species:
human : 137
Page Size
Current 25
  Page 1 of 6
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanGPRC6A222545G protein-coupled receptor, family C, group 6, member A
INFERRED
HumanMPZL3196264myelin protein zero-like 3
INFERRED
HumanTMPRSS6164656transmembrane protease, serine 6
INFERRED
HumanPHOSPHO1162466phosphatase, orphan 1
INFERRED
HumanSLC30A7148867solute carrier family 30 (zinc transporter), member 7
Click here to display 10 evidence detail records.
HumanHFE2148738hemochromatosis type 2 (juvenile)
INFERRED
HumanSLC34A3142680solute carrier family 34 (type II sodium/phosphate contransporter), member 3
INFERRED
HumanTRPM6140803transient receptor potential cation channel, subfamily M, member 6
INFERRED
HumanBTBD9114781BTB (POZ) domain containing 9
INFERRED
HumanFOXP293986forkhead box P2
Click here to display 10 evidence detail records.
HumanPLVAP83483plasmalemma vesicle associated protein
INFERRED
HumanWNK465266WNK lysine deficient protein kinase 4
INFERRED
HumanWNK165125WNK lysine deficient protein kinase 1
INFERRED
HumanTMEM2757393transmembrane protein 27
INFERRED
HumanTTC7A57217tetratricopeptide repeat domain 7A
INFERRED
HumanFAM20C56975family with sequence similarity 20, member C
INFERRED
HumanSLC2A956606solute carrier family 2 (facilitated glucose transporter), member 9
INFERRED
HumanTRPV556302transient receptor potential cation channel, subfamily V, member 5
INFERRED
HumanTRPV655503transient receptor potential cation channel, subfamily V, member 6
INFERRED
HumanSTEAP355240STEAP family member 3, metalloreductase
INFERRED
HumanEXOC654536exocyst complex component 6
INFERRED
HumanFXYD453828FXYD domain containing ion transport regulator 4
INFERRED
HumanWWOX51741WW domain containing oxidoreductase
INFERRED
HumanRHCG51458Rh family, C glycoprotein
INFERRED
HumanATP6V0A450617ATPase, H+ transporting, lysosomal V0 subunit a4
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0006357abnormal circulating mineral level0self