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Details
Link-It Detail - Jax Mouse Phenotype - abnormal Peyer's patch number
Debug Stats
  • ### Total Build Time: 66 ms 16.119 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 386 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 306 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 192 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=7 ms Completed: 7 ms rowSize= 588 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.029 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=8 ms Completed: 8 ms rowSize= 1.578 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=31 ms Completed: 31 ms rowSize= 10.763 KB
  • CONCEPT_XREFS gt=7 ms Completed: 7 ms rowSize= 1.167 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal Peyer's patch number MP:0008131
Definition (1)
anomaly in the number of the protruding lymphoid tissue located on the mucosa of the small intestine that is composed of densely packed B cell follicles
Synonyms (1)
"abnormal number of Peyer's patches" EXACT
Parents (1)
img abnormal Peyer's patch morphology MP:0000696
Children (2)
img decreased Peyer's patch number MP:0008133
img increased Peyer's patch number MP:0008132
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img immune system phenotype MP:00053877img abnormal Peyer's patch morphology MP:0000696
Genes (22)

Species:
human : 22
SpeciesGeneGeneIdGene NameEvidence
HumanGCSAM257144germinal center-associated, signaling and motility
INFERRED
HumanNKX2-3159296
INFERRED
HumanSPPL2A84888signal peptide peptidase like 2A
INFERRED
HumanNOD264127nucleotide-binding oligomerization domain containing 2
INFERRED
HumanSASH354440SAM and SH3 domain containing 3
INFERRED
HumanDDX5823586DEAD (Asp-Glu-Ala-Asp) box polypeptide 58
INFERRED
HumanCXCL1310563chemokine (C-X-C motif) ligand 13
INFERRED
HumanTOX9760thymocyte selection-associated high mobility group box
INFERRED
HumanTNFRSF11A8792tumor necrosis factor receptor superfamily, member 11a, NFKB activator
INFERRED
HumanTNFRSF1A7132tumor necrosis factor receptor superfamily, member 1A
INFERRED
HumanTNF7124tumor necrosis factor
INFERRED
HumanRELB5971v-rel avian reticuloendotheliosis viral oncogene homolog B
INFERRED
HumanNFKBIA4792nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha
INFERRED
HumanNFKB14790nuclear factor of kappa light polypeptide gene enhancer in B-cells 1
INFERRED
HumanITGA43676integrin, alpha 4 (antigen CD49D, alpha 4 subunit of VLA-4 receptor)
INFERRED
HumanGFRA12674GDNF family receptor alpha 1
INFERRED
HumanCTNNB11499catenin (cadherin-associated protein), beta 1, 88kDa
INFERRED
HumanCCR61235chemokine (C-C motif) receptor 6
INFERRED
HumanCBFB865core-binding factor, beta subunit
INFERRED
HumanRUNX1861runt-related transcription factor 1
INFERRED
HumanCACNB4785calcium channel, voltage-dependent, beta 4 subunit
INFERRED
HumanBCL3602B-cell CLL/lymphoma 3
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0008131abnormal Peyer's patch number0self