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Details
Link-It Detail - Jax Mouse Phenotype - abnormal mineral level
Debug Stats
  • ### Total Build Time: 33 ms 21.336 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 372 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 251 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= 583 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.920 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.582 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=25 ms Completed: 25 ms rowSize= 15.352 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.160 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal mineral level MP:0000192
Definition (1)
any anomaly in the concentration of any inorganic substance that has importance in body functions
Parents (1)
img abnormal mineral homeostasis MP:0005636
Children (4)
img abnormal circulating mineral level MP:0006357
img abnormal copper level MP:0003952
img abnormal iron level MP:0001770
img abnormal selenium level MP:0001775
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053765img abnormal mineral homeostasis MP:0005636
Genes (185)

Species:
human : 185
Page Size
Current 25
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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
HumanCOMMD1150684copper metabolism (Murr1) domain containing 1
INFERRED
HumanSLC30A7148867solute carrier family 30 (zinc transporter), member 7
INFERRED
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
HumanSPIC121599Spi-C transcription factor (Spi-1/PU.1 related)
INFERRED
HumanBTBD9114781BTB (POZ) domain containing 9
INFERRED
HumanFOXP293986forkhead box P2
INFERRED
HumanPLVAP83483plasmalemma vesicle associated protein
INFERRED
HumanCYBRD179901cytochrome b reductase 1
INFERRED
HumanWNK465266WNK lysine deficient protein kinase 4
INFERRED
HumanWNK165125WNK lysine deficient protein kinase 1
INFERRED
HumanTMEM2757393transmembrane protein 27
INFERRED
HumanTTC7A57217tetratricopeptide repeat domain 7A
Click here to display 15 evidence detail records.
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
HumanANKH56172ANKH inorganic pyrophosphate transport regulator
INFERRED
HumanSLC39A455630solute carrier family 39 (zinc transporter), member 4
INFERRED
HumanTRPV655503transient receptor potential cation channel, subfamily V, member 6
Click here to display 15 evidence detail records.
HumanSTEAP355240STEAP family member 3, metalloreductase
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000192abnormal mineral level0self