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Details
Link-It Detail - Jax Mouse Phenotype - abnormal digestion
Debug Stats
  • ### Total Build Time: 112 ms 21.225 KB
  • CONCEPT_NAME gt=9 ms Completed: 9 ms rowSize= 364 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 363 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 185 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=57 ms Completed: 57 ms rowSize= 591 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 1.896 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.588 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=37 ms Completed: 37 ms rowSize= 14.973 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.156 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal digestion MP:0001664
Definition (1)
any anomaly of the physical, chemical, and biochemical processes carried out by multicellular organisms to break down ingested nutrients into components that may be easily absorbed and directed into metabolism
Synonyms (1)
"abnormal digestive function" EXACT
Parents (1)
img abnormal digestive system physiology MP:0001663
Children (4)
img abnormal intestinal absorption MP:0001666
img abnormal digestive secretion MP:0000501
img nausea MP:0003259
img vomiting MP:0003260
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img digestive/alimentary phenotype MP:00053814img abnormal digestive system physiology MP:0001663
Genes (91)

Species:
human : 91
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSLC9A4389015solute carrier family 9, subfamily A (NHE4, cation proton antiporter 4), member 4
INFERRED
HumanPTF1A256297pancreas specific transcription factor, 1a
Click here to display 14 evidence detail records.
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
INFERRED
HumanTRIM50135892tripartite motif containing 50
INFERRED
HumanSLC26A9115019solute carrier family 26 (anion exchanger), member 9
INFERRED
HumanFOXQ194234forkhead box Q1
INFERRED
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
HumanSYTL254843synaptotagmin-like 2
INFERRED
HumanSLC2A829988solute carrier family 2 (facilitated glucose transporter), member 8
INFERRED
HumanNPC1L129881NPC1-like 1
INFERRED
HumanATE111101arginyltransferase 1
INFERRED
HumanKCNE29992potassium voltage-gated channel, Isk-related family, member 2
INFERRED
HumanSLC23A19963solute carrier family 23 (ascorbic acid transporter), member 1
INFERRED
HumanCLOCK9575clock circadian regulator
INFERRED
HumanGCNT39245glucosaminyl (N-acetyl) transferase 3, mucin type
INFERRED
HumanMBTPS18720membrane-bound transcription factor peptidase, site 1
INFERRED
HumanDGAT18694diacylglycerol O-acyltransferase 1
Click here to display 14 evidence detail records.
HumanSOAT28435sterol O-acyltransferase 2
INFERRED
HumanNR0B28431nuclear receptor subfamily 0, group B, member 2
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001664abnormal digestion0self