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Details
Link-It Detail - Jax Mouse Phenotype - abnormal circulating magnesium level
Debug Stats
  • ### Total Build Time: 19 ms 17.324 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 400 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 205 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 182 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= 1.035 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 1.043 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 4.296 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=17 ms Completed: 17 ms rowSize= 8.863 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.174 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal circulating magnesium level MP:0001771
Definition (1)
any anomaly in the blood concentration of magnesium
Synonyms (1)
"abnormal magnesium level" EXACT
Parents (2)
img abnormal magnesium ion homeostasis MP:0011979
img abnormal circulating mineral level MP:0006357
Children (2)
img increased circulating magnesium level MP:0010092
img decreased circulating magnesium level MP:0010093
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053766img abnormal magnesium ion homeostasis MP:0011979
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053767img abnormal circulating mineral level MP:0006357
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053766img abnormal circulating mineral level MP:0006357
Genes (12)

Species:
human : 12
SpeciesGeneGeneIdGene NameEvidence
HumanTRPM6140803transient receptor potential cation channel, subfamily M, member 6
INFERRED
HumanWNK465266WNK lysine deficient protein kinase 4
INFERRED
HumanSLC2A956606solute carrier family 2 (facilitated glucose transporter), member 9
INFERRED
HumanSTK3927347serine threonine kinase 39
INFERRED
HumanCLDN1610686claudin 16
INFERRED
HumanCLDN109071claudin 10
INFERRED
HumanSLC12A36559solute carrier family 12 (sodium/chloride transporter), member 3
INFERRED
HumanSLC12A16557solute carrier family 12 (sodium/potassium/chloride transporter), member 1
img Jax MP, Pubmed Id: 17215439, MOUSE PHENOTYPE ID: MGI:103150
img Jax MP, Pubmed Id: 12488435, MOUSE PHENOTYPE ID: MGI:2151253
HumanCASR846calcium-sensing receptor
INFERRED
HumanCALCA796calcitonin-related polypeptide alpha
img Jax MP, Pubmed Id: 12488435, MOUSE PHENOTYPE ID: MGI:2151253
img Jax MP, Pubmed Id: 17215439, MOUSE PHENOTYPE ID: MGI:103150
HumanBBS4585Bardet-Biedl syndrome 4
INFERRED
HumanAKR1B1231aldo-keto reductase family 1, member B1 (aldose reductase)
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001771abnormal circulating magnesium level0self