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Details
Link-It Detail - Jax Mouse Phenotype - abnormal circulating sodium level
Debug Stats
  • ### Total Build Time: 61 ms 19.651 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 394 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 319 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 179 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 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= 1.032 KB
  • CONCEPT_CHILDREN gt=7 ms Completed: 7 ms rowSize= 1.037 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 4.293 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=42 ms Completed: 42 ms rowSize= 11.103 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.171 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal circulating sodium level MP:0001776
Definition (1)
any anomaly in the concentration in the blood of sodium, the most plentiful extracellular ion in the body and the principal determinant of extracellular fluid volume
Synonyms (1)
"abnormal sodium level" EXACT
Parents (2)
img abnormal sodium ion homeostasis MP:0011977
img abnormal circulating mineral level MP:0006357
Children (2)
img decreased circulating sodium level MP:0005634
img increased circulating sodium level MP:0005633
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053766img abnormal sodium ion homeostasis MP:0011977
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 (21)

Species:
human : 21
SpeciesGeneGeneIdGene NameEvidence
HumanWNK165125WNK lysine deficient protein kinase 1
INFERRED
HumanTMEM2757393transmembrane protein 27
INFERRED
HumanWWOX51741WW domain containing oxidoreductase
INFERRED
HumanSLCO1B328234solute carrier organic anion transporter family, member 1B3
INFERRED
HumanNEDD4L23327neural precursor cell expressed, developmentally down-regulated 4-like, E3 ubiquitin protein ligase
INFERRED
HumanHSPA4L22824heat shock 70kDa protein 4-like
INFERRED
HumanTXNIP10628thioredoxin interacting protein
INFERRED
HumanSLC4A48671solute carrier family 4 (sodium bicarbonate cotransporter), member 4
INFERRED
HumanBSND7809Bartter syndrome, infantile, with sensorineural deafness (Barttin)
INFERRED
HumanSLC12A16557solute carrier family 12 (sodium/potassium/chloride transporter), member 1
INFERRED
HumanSLC5A26524solute carrier family 5 (sodium/glucose cotransporter), member 2
INFERRED
HumanSCNN1G6340sodium channel, non-voltage-gated 1, gamma subunit
INFERRED
HumanSCNN1B6338sodium channel, non-voltage-gated 1, beta subunit
INFERRED
HumanNR3C24306nuclear receptor subfamily 3, group C, member 2
INFERRED
HumanKCNJ13758potassium inwardly-rectifying channel, subfamily J, member 1
INFERRED
HumanKCNE13753potassium voltage-gated channel, Isk-related family, member 1
INFERRED
HumanGUCA2B2981guanylate cyclase activator 2B (uroguanylin)
INFERRED
HumanSLC26A31811solute carrier family 26 (anion exchanger), member 3
INFERRED
HumanCYP11A11583cytochrome P450, family 11, subfamily A, polypeptide 1
img Jax MP, Pubmed Id: 12145347, MOUSE PHENOTYPE ID: MGI:88582
HumanBBS4585Bardet-Biedl syndrome 4
INFERRED
HumanAVPR2554arginine vasopressin receptor 2
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001776abnormal circulating sodium level0self