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Details
Link-It Detail - Jax Mouse Phenotype - abnormal small intestine morphology
Debug Stats
  • ### Total Build Time: 258 ms 23.857 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 398 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 294 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 183 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= 584 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 3.340 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.581 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=252 ms Completed: 252 ms rowSize= 16.194 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.173 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal small intestine morphology MP:0000496
Definition (1)
any structural anomaly of the portion of the digestive tube between the stomach and the cecum, consisting of the duodenum, ileum and jejunum
Synonyms (1)
"small intestine dysplasia" EXACT
Parents (1)
img abnormal intestine morphology MP:0000477
Children (7)
img abnormal small intestine crypts of Lieberkuhn morphology MP:0004841
img abnormal small intestinal villus morphology MP:0008108
img abnormal duodenum morphology MP:0003271
img abnormal jejunum morphology MP:0004002
img abnormal ileum morphology MP:0002581
img abnormal small intestine placement MP:0000497
img small intestinal prolapse MP:0000500
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img digestive/alimentary phenotype MP:00053815img abnormal intestine morphology MP:0000477
Genes (138)

Species:
human : 138
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanAREGB727738amphiregulin B
Click here to display 101 evidence detail records.
HumanENPP7339221ectonucleotide pyrophosphatase/phosphodiesterase 7
INFERRED
HumanYIPF6286451Yip1 domain family, member 6
Click here to display 101 evidence detail records.
HumanPTF1A256297pancreas specific transcription factor, 1a
INFERRED
HumanSLC51A200931solute carrier family 51, alpha subunit
Click here to display 101 evidence detail records.
HumanPIKFYVE200576phosphoinositide kinase, FYVE finger containing
INFERRED
HumanNKX2-3159296
Click here to display 101 evidence detail records.
HumanRC3H1149041ring finger and CCCH-type domains 1
INFERRED
HumanTWIST2117581twist basic helix-loop-helix transcription factor 2
Click here to display 101 evidence detail records.
HumanPYGO290780pygopus homolog 2 (Drosophila)
Click here to display 101 evidence detail records.
HumanGADD45GIP190480growth arrest and DNA-damage-inducible, gamma interacting protein 1
INFERRED
HumanNKD185407naked cuticle homolog 1 (Drosophila)
Click here to display 101 evidence detail records.
HumanTNS364759tensin 3
INFERRED
HumanSAV160485salvador homolog 1 (Drosophila)
INFERRED
HumanHR55806hair growth associated
INFERRED
HumanSLC39A455630solute carrier family 39 (zinc transporter), member 4
INFERRED
HumanFERMT155612fermitin family member 1
INFERRED
HumanLGR455366leucine-rich repeat containing G protein-coupled receptor 4
INFERRED
HumanATG16L155054autophagy related 16-like 1 (S. cerevisiae)
INFERRED
HumanRNF4354894ring finger protein 43
INFERRED
HumanTDP251567tyrosyl-DNA phosphodiesterase 2
INFERRED
HumanCLEC1B51266C-type lectin domain family 1, member B
Click here to display 101 evidence detail records.
HumanICOS29851inducible T-cell co-stimulator
Click here to display 101 evidence detail records.
HumanBSCL226580Berardinelli-Seip congenital lipodystrophy 2 (seipin)
Click here to display 101 evidence detail records.
HumanSPDEF25803SAM pointed domain containing ETS transcription factor
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0000496abnormal small intestine morphology0self