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Details
Link-It Detail - Jax Mouse Phenotype - abnormal intestinal cholesterol absorption
Debug Stats
  • ### Total Build Time: 22 ms 13.551 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 412 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 269 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=5 ms Completed: 5 ms rowSize= 591 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.055 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.943 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=9 ms Completed: 9 ms rowSize= 6.986 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.180 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal intestinal cholesterol absorption MP:0002645
Definition (1)
any anomaly in the ability of the body to take up cholesterol into the blood by absorption from the small intestine
Parents (1)
img abnormal intestinal lipid absorption MP:0005342
Children (2)
img decreased intestinal cholesterol absorption MP:0002647
img increased intestinal cholesterol absorption MP:0002646
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img homeostasis/metabolism phenotype MP:00053766img abnormal intestinal lipid absorption MP:0005342
img mammalian phenotype MP:0000001img digestive/alimentary phenotype MP:00053817img abnormal intestinal lipid absorption MP:0005342
Genes (14)

Species:
human : 14
SpeciesGeneGeneIdGene NameEvidence
HumanHSD3B780270hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7
INFERRED
HumanNPC1L129881NPC1-like 1
INFERRED
HumanSOAT28435sterol O-acyltransferase 2
INFERRED
HumanNR0B28431nuclear receptor subfamily 0, group B, member 2
INFERRED
HumanSLC10A26555solute carrier family 10 (sodium/bile acid cotransporter), member 2
INFERRED
HumanPNLIP5406pancreatic lipase
INFERRED
HumanABCB45244ATP-binding cassette, sub-family B (MDR/TAP), member 4
INFERRED
HumanMUC14582mucin 1, cell surface associated
INFERRED
HumanCYP8B11582cytochrome P450, family 8, subfamily B, polypeptide 1
INFERRED
HumanCYP7A11581cytochrome P450, family 7, subfamily A, polypeptide 1
INFERRED
HumanCEL1056carboxyl ester lipase
INFERRED
HumanCD36948CD36 molecule (thrombospondin receptor)
INFERRED
HumanCCKAR886cholecystokinin A receptor
INFERRED
HumanABCA119ATP-binding cassette, sub-family A (ABC1), member 1
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0002645abnormal intestinal cholesterol absorption0self