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Details
Link-It Detail - Jax Mouse Phenotype - abnormal intestinal peristalsis
Debug Stats
  • ### Total Build Time: 44 ms 55.105 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 390 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 321 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= 589 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 1.023 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=9 ms Completed: 9 ms rowSize= 1.586 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=19 ms Completed: 19 ms rowSize= 49.913 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.169 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal intestinal peristalsis MP:0003289
Definition (1)
altered intestinal movement characterized by waves of alternate circular contraction and relaxation of the muscular walls of the bowel that move bowel contents forward
Parents (1)
img abnormal gastrointestinal motility MP:0011082
Children (2)
img intestinal hypoperistalsis MP:0003290
img interstinal hyperperistalsis MP:0003291
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img digestive/alimentary phenotype MP:00053815img abnormal gastrointestinal motility MP:0011082
Genes (19)

Species:
human : 19
SpeciesGeneGeneIdGene NameEvidence
HumanNKX2-3159296
img Jax MP, Pubmed Id: 18586037, MOUSE PHENOTYPE ID: MGI:106012
img Jax MP, Pubmed Id: 19914172, MOUSE PHENOTYPE ID: MGI:2447072
img Jax MP, Pubmed Id: 11371512, MOUSE PHENOTYPE ID: MGI:97783
img Jax MP, Pubmed Id: 21949878, MOUSE PHENOTYPE ID: MGI:1338038
img Jax MP, Pubmed Id: 10926756, MOUSE PHENOTYPE ID: MGI:97348
img Jax MP, Pubmed Id: 10675330, MOUSE PHENOTYPE ID: MGI:97902
img Jax MP, Pubmed Id: 9606187, MOUSE PHENOTYPE ID: MGI:108174
img Jax MP, Pubmed Id: 16227613, MOUSE PHENOTYPE ID: MGI:97902
HumanAEBP2121536AE binding protein 2
img Jax MP, Pubmed Id: 10675330, MOUSE PHENOTYPE ID: MGI:97902
img Jax MP, Pubmed Id: 18586037, MOUSE PHENOTYPE ID: MGI:106012
img Jax MP, Pubmed Id: 11371512, MOUSE PHENOTYPE ID: MGI:97783
img Jax MP, Pubmed Id: 16227613, MOUSE PHENOTYPE ID: MGI:97902
img Jax MP, Pubmed Id: 21949878, MOUSE PHENOTYPE ID: MGI:1338038
img Jax MP, Pubmed Id: 9606187, MOUSE PHENOTYPE ID: MGI:108174
img Jax MP, Pubmed Id: 19914172, MOUSE PHENOTYPE ID: MGI:2447072
img Jax MP, Pubmed Id: 10926756, MOUSE PHENOTYPE ID: MGI:97348
HumanKIF26A26153kinesin family member 26A
img Jax MP, Pubmed Id: 21949878, MOUSE PHENOTYPE ID: MGI:1338038
img Jax MP, Pubmed Id: 11371512, MOUSE PHENOTYPE ID: MGI:97783
img Jax MP, Pubmed Id: 10926756, MOUSE PHENOTYPE ID: MGI:97348
img Jax MP, Pubmed Id: 10675330, MOUSE PHENOTYPE ID: MGI:97902
img Jax MP, Pubmed Id: 16227613, MOUSE PHENOTYPE ID: MGI:97902
img Jax MP, Pubmed Id: 9606187, MOUSE PHENOTYPE ID: MGI:108174
img Jax MP, Pubmed Id: 19914172, MOUSE PHENOTYPE ID: MGI:2447072
img Jax MP, Pubmed Id: 18586037, MOUSE PHENOTYPE ID: MGI:106012
HumanTAGLN6876transgelin
img Jax MP, Pubmed Id: 21949878, MOUSE PHENOTYPE ID: MGI:1338038
img Jax MP, Pubmed Id: 10926756, MOUSE PHENOTYPE ID: MGI:97348
img Jax MP, Pubmed Id: 11371512, MOUSE PHENOTYPE ID: MGI:97783
img Jax MP, Pubmed Id: 10675330, MOUSE PHENOTYPE ID: MGI:97902
img Jax MP, Pubmed Id: 16227613, MOUSE PHENOTYPE ID: MGI:97902
img Jax MP, Pubmed Id: 9606187, MOUSE PHENOTYPE ID: MGI:108174
img Jax MP, Pubmed Id: 19914172, MOUSE PHENOTYPE ID: MGI:2447072
img Jax MP, Pubmed Id: 18586037, MOUSE PHENOTYPE ID: MGI:106012
HumanSMTN6525smoothelin
INFERRED
HumanRET5979ret proto-oncogene
img Jax MP, Pubmed Id: 21949878, MOUSE PHENOTYPE ID: MGI:1338038
img Jax MP, Pubmed Id: 19914172, MOUSE PHENOTYPE ID: MGI:2447072
img Jax MP, Pubmed Id: 11371512, MOUSE PHENOTYPE ID: MGI:97783
img Jax MP, Pubmed Id: 16227613, MOUSE PHENOTYPE ID: MGI:97902
img Jax MP, Pubmed Id: 10675330, MOUSE PHENOTYPE ID: MGI:97902
img Jax MP, Pubmed Id: 10926756, MOUSE PHENOTYPE ID: MGI:97348
img Jax MP, Pubmed Id: 18586037, MOUSE PHENOTYPE ID: MGI:106012
img Jax MP, Pubmed Id: 9606187, MOUSE PHENOTYPE ID: MGI:108174
HumanPSAP5660prosaposin
img Jax MP, Pubmed Id: 10926756, MOUSE PHENOTYPE ID: MGI:97348
img Jax MP, Pubmed Id: 11371512, MOUSE PHENOTYPE ID: MGI:97783
img Jax MP, Pubmed Id: 16227613, MOUSE PHENOTYPE ID: MGI:97902
img Jax MP, Pubmed Id: 19914172, MOUSE PHENOTYPE ID: MGI:2447072
img Jax MP, Pubmed Id: 21949878, MOUSE PHENOTYPE ID: MGI:1338038
img Jax MP, Pubmed Id: 10675330, MOUSE PHENOTYPE ID: MGI:97902
img Jax MP, Pubmed Id: 18586037, MOUSE PHENOTYPE ID: MGI:106012
img Jax MP, Pubmed Id: 9606187, MOUSE PHENOTYPE ID: MGI:108174
HumanPRKG15592protein kinase, cGMP-dependent, type I
img Jax MP, Pubmed Id: 16227613, MOUSE PHENOTYPE ID: MGI:97902
img Jax MP, Pubmed Id: 19914172, MOUSE PHENOTYPE ID: MGI:2447072
img Jax MP, Pubmed Id: 9606187, MOUSE PHENOTYPE ID: MGI:108174
img Jax MP, Pubmed Id: 18586037, MOUSE PHENOTYPE ID: MGI:106012
img Jax MP, Pubmed Id: 21949878, MOUSE PHENOTYPE ID: MGI:1338038
img Jax MP, Pubmed Id: 10926756, MOUSE PHENOTYPE ID: MGI:97348
img Jax MP, Pubmed Id: 10675330, MOUSE PHENOTYPE ID: MGI:97902
img Jax MP, Pubmed Id: 11371512, MOUSE PHENOTYPE ID: MGI:97783
HumanPRKAR1A5573protein kinase, cAMP-dependent, regulatory, type I, alpha
INFERRED
HumanNTSR14923neurotensin receptor 1 (high affinity)
INFERRED
HumanNRTN4902neurturin
INFERRED
HumanMYH114629myosin, heavy chain 11, smooth muscle
INFERRED
HumanGUCY1B32983guanylate cyclase 1, soluble, beta 3
INFERRED
HumanGFRA22675GDNF family receptor alpha 2
INFERRED
HumanGFRA12674GDNF family receptor alpha 1
INFERRED
HumanGDNF2668glial cell derived neurotrophic factor
INFERRED
HumanEGFR1956epidermal growth factor receptor
INFERRED
HumanDLX21746distal-less homeobox 2
INFERRED
HumanCHRNB21141cholinergic receptor, nicotinic, beta 2 (neuronal)
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0003289abnormal intestinal peristalsis0self