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Details
Link-It Detail - Jax Mouse Phenotype - abnormal vitamin homeostasis
Debug Stats
  • ### Total Build Time: 126 ms 23.144 KB
  • CONCEPT_NAME gt=8 ms Completed: 8 ms rowSize= 384 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 370 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=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=5 ms Completed: 5 ms rowSize= 575 bytes
  • CONCEPT_CHILDREN gt=74 ms Completed: 74 ms rowSize= 1.930 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.574 KB
  • CONCEPT_RELATIONSHIPS gt=2 ms Completed: 2 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=31 ms Completed: 31 ms rowSize= 17.031 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.166 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal vitamin homeostasis MP:0004019
Definition (1)
anomaly in the processes involved in the maintenance of an internal equilibrium of organic substances found in food and are not synthesized by the body and are necessary in trace amounts for normal metabolic function
Parents (1)
img abnormal homeostasis MP:0001764
Children (4)
img abnormal vitamin A metabolism MP:0011233
img abnormal vitamin level MP:0005400
img abnormal response to vitamins MP:0003639
img abnormal vitamin absorption MP:0001671
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053764img abnormal homeostasis MP:0001764
Genes (50)

Species:
human : 50
Page Size
Current 25
  Page 1 of 2
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanKCP375616kielin/chordin-like protein
INFERRED
HumanRDH10157506retinol dehydrogenase 10 (all-trans)
INFERRED
HumanSLC34A3142680solute carrier family 34 (type II sodium/phosphate contransporter), member 3
INFERRED
HumanRBP7116362retinol binding protein 7, cellular
INFERRED
HumanSTRA664220stimulated by retinoic acid 6
INFERRED
HumanFAM20C56975family with sequence similarity 20, member C
INFERRED
HumanTRPV556302transient receptor potential cation channel, subfamily V, member 5
INFERRED
HumanTRPV655503transient receptor potential cation channel, subfamily V, member 6
INFERRED
HumanBCMO153630beta-carotene 15,15'-monooxygenase 1
img Jax MP, Pubmed Id: 20200446, MOUSE PHENOTYPE ID: MGI:1341903
img Jax MP, Pubmed Id: 17855355, MOUSE PHENOTYPE ID: MGI:1926923
HumanSIK323387SIK family kinase 3
INFERRED
HumanCLDN1610686claudin 16
INFERRED
HumanMTHFS105885,10-methenyltetrahydrofolate synthetase (5-formyltetrahydrofolate cyclo-ligase)
INFERRED
HumanSLC34A210568solute carrier family 34 (type II sodium/phosphate contransporter), member 2
INFERRED
HumanAKR1A110327aldo-keto reductase family 1, member A1 (aldehyde reductase)
INFERRED
HumanSLC23A19963solute carrier family 23 (ascorbic acid transporter), member 1
img Jax MP, Pubmed Id: 17855355, MOUSE PHENOTYPE ID: MGI:1926923
img Jax MP, Pubmed Id: 20200446, MOUSE PHENOTYPE ID: MGI:1341903
HumanSLC23A29962solute carrier family 23 (ascorbic acid transporter), member 2
INFERRED
HumanKL9365klotho
INFERRED
HumanLRAT9227lecithin retinol acyltransferase (phosphatidylcholine--retinol O-acyltransferase)
INFERRED
HumanRGN9104regucalcin
INFERRED
HumanALDH1A28854aldehyde dehydrogenase 1 family, member A2
INFERRED
HumanDGAT18694diacylglycerol O-acyltransferase 1
INFERRED
HumanFGF238074fibroblast growth factor 23
INFERRED
HumanVDR7421vitamin D (1,25- dihydroxyvitamin D3) receptor
INFERRED
HumanTTR7276transthyretin
INFERRED
HumanTTPA7274tocopherol (alpha) transfer protein
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004019abnormal vitamin homeostasis0self