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Details
Link-It Detail - Jax Mouse Phenotype - abnormal vitamin D level
Debug Stats
  • ### Total Build Time: 85 ms 14.555 KB
  • CONCEPT_NAME gt=9 ms Completed: 9 ms rowSize= 376 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 455 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 184 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=6 ms Completed: 6 ms rowSize= 589 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=15 ms Completed: 15 ms rowSize= 1.588 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=51 ms Completed: 51 ms rowSize= 10.086 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.162 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal vitamin D level MP:0011228
Definition (1)
any anomaly in the concentration of vitamin D, any of a group of related, fat-soluble compounds that are derived from delta-5,7 steroids and play a central role in calcium metabolism; specific forms of vitamin D include calciferol (ergocalciferol; vitamin D2) and cholecalciferol (calciol; vitamin D3)
Synonyms (1)
"abnormal vitamin D3 level" NARROW
Parents (1)
img abnormal fat-soluble vitamin level MP:0005401
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053767img abnormal fat-soluble vitamin level MP:0005401
Genes (16)

Species:
human : 16
SpeciesGeneGeneIdGene NameEvidence
HumanSLC34A3142680solute carrier family 34 (type II sodium/phosphate contransporter), member 3
Click here to display 32 evidence detail records.
HumanFAM20C56975family with sequence similarity 20, member C
Click here to display 32 evidence detail records.
HumanTRPV556302transient receptor potential cation channel, subfamily V, member 5
Click here to display 32 evidence detail records.
HumanTRPV655503transient receptor potential cation channel, subfamily V, member 6
Click here to display 32 evidence detail records.
HumanCLDN1610686claudin 16
Click here to display 32 evidence detail records.
HumanSLC34A210568solute carrier family 34 (type II sodium/phosphate contransporter), member 2
Click here to display 32 evidence detail records.
HumanKL9365klotho
Click here to display 32 evidence detail records.
HumanFGF238074fibroblast growth factor 23
Click here to display 32 evidence detail records.
HumanVDR7421vitamin D (1,25- dihydroxyvitamin D3) receptor
Click here to display 32 evidence detail records.
HumanSLC34A16569solute carrier family 34 (type II sodium/phosphate contransporter), member 1
Click here to display 32 evidence detail records.
HumanPHEX5251phosphate regulating endopeptidase homolog, X-linked
Click here to display 32 evidence detail records.
HumanGC2638group-specific component (vitamin D binding protein)
Click here to display 32 evidence detail records.
HumanGALNT32591UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 3 (GalNAc-T3)
Click here to display 32 evidence detail records.
HumanEPHB62051EPH receptor B6
Click here to display 32 evidence detail records.
HumanCYP27A11593cytochrome P450, family 27, subfamily A, polypeptide 1
Click here to display 32 evidence detail records.
HumanCYP24A11591cytochrome P450, family 24, subfamily A, polypeptide 1
Click here to display 32 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0011228abnormal vitamin D level0self