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Details
Link-It Detail - Jax Mouse Phenotype - abnormal intestinal absorption
Debug Stats
  • ### Total Build Time: 27 ms 21.121 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 388 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 249 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 186 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= 573 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.955 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.570 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=22 ms Completed: 22 ms rowSize= 14.920 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.168 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal intestinal absorption MP:0001666
Definition (1)
any anomaly in the quantity or rate of any nutrient taken up from the contents of the intestine
Synonyms (1)
"abnormal nutrient absorption" EXACT
Parents (1)
img abnormal digestion MP:0001664
Children (4)
img abnormal vitamin absorption MP:0001671
img abnormal carbohydrate absorption MP:0001667
img abnormal intestinal mineral absorption MP:0001670
img abnormal intestinal lipid absorption MP:0005342
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img digestive/alimentary phenotype MP:00053815img abnormal digestion MP:0001664
Genes (49)

Species:
human : 49
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanTMPRSS6164656transmembrane protease, serine 6
INFERRED
HumanSLC30A7148867solute carrier family 30 (zinc transporter), member 7
INFERRED
HumanSLC34A3142680solute carrier family 34 (type II sodium/phosphate contransporter), member 3
Click here to display 22 evidence detail records.
HumanHSD3B780270hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7
INFERRED
HumanMOGAT280168monoacylglycerol O-acyltransferase 2
INFERRED
HumanABCG864241ATP-binding cassette, sub-family G (WHITE), member 8
INFERRED
HumanABCG564240ATP-binding cassette, sub-family G (WHITE), member 5
INFERRED
HumanTRPV655503transient receptor potential cation channel, subfamily V, member 6
INFERRED
HumanSLC2A829988solute carrier family 2 (facilitated glucose transporter), member 8
INFERRED
HumanNPC1L129881NPC1-like 1
INFERRED
HumanATE111101arginyltransferase 1
Click here to display 22 evidence detail records.
HumanSLC23A19963solute carrier family 23 (ascorbic acid transporter), member 1
INFERRED
HumanCLOCK9575clock circadian regulator
Click here to display 22 evidence detail records.
HumanGCNT39245glucosaminyl (N-acetyl) transferase 3, mucin type
Click here to display 22 evidence detail records.
HumanMBTPS18720membrane-bound transcription factor peptidase, site 1
INFERRED
HumanSOAT28435sterol O-acyltransferase 2
INFERRED
HumanNR0B28431nuclear receptor subfamily 0, group B, member 2
INFERRED
HumanVDR7421vitamin D (1,25- dihydroxyvitamin D3) receptor
INFERRED
HumanTFRC7037transferrin receptor (p90, CD71)
INFERRED
HumanSLC15A16564solute carrier family 15 (oligopeptide transporter), member 1
Click here to display 22 evidence detail records.
HumanSLC10A26555solute carrier family 10 (sodium/bile acid cotransporter), member 2
INFERRED
HumanRSC1A16248regulatory solute carrier protein, family 1, member 1
INFERRED
HumanRBP25948retinol binding protein 2, cellular
INFERRED
HumanPNLIPRP25408pancreatic lipase-related protein 2
INFERRED
HumanPNLIP5406pancreatic lipase
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001666abnormal intestinal absorption0self