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Details
Link-It Detail - Jax Mouse Phenotype - abnormal developmental patterning
Debug Stats
  • ### Total Build Time: 400 ms 23.604 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 394 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 222 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 211 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= 590 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 4.259 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.580 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=390 ms Completed: 390 ms rowSize= 15.066 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.171 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal developmental patterning MP:0002084
Definition (1)
abnormal systematic arrangement of the developing body along an axis
Synonyms (1)
"embryogenesis: developmental patterning abnormalities" EXACT
Parents (1)
img abnormal embryogenesis/ development MP:0001672
Children (9)
img abnormal primitive streak morphology MP:0002231
img abnormal rostral-caudal axis patterning MP:0005221
img abnormal dorsal-ventral axis patterning MP:0001704
img abnormal gastrulation MP:0001695
img mirror image duplication MP:0009470
img abnormal prechordal plate morphology MP:0004387
img abnormal triploblastic development MP:0001674
img abnormal proximal-distal axis patterning MP:0001705
img abnormal left-right axis patterning MP:0001706
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img embryogenesis phenotype MP:00053804img abnormal embryogenesis/ development MP:0001672
Genes (432)

Species:
human : 432
Page Size
Current 25
  Page 1 of 18
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSCXA100129885scleraxis homolog A (mouse)
INFERRED
HumanCFC1B653275cripto, FRL-1, cryptic family 1B
INFERRED
HumanSCXB642658scleraxis homolog B (mouse)
INFERRED
HumanNOTO344022notochord homeobox
INFERRED
HumanMSGN1343930mesogenin 1
INFERRED
HumanRSPO2340419R-spondin 2
INFERRED
HumanCRB2286204crumbs homolog 2 (Drosophila)
INFERRED
HumanDPH3285381diphthamide biosynthesis 3
INFERRED
HumanLAMA1284217laminin, alpha 1
INFERRED
HumanIPMK253430inositol polyphosphate multikinase
INFERRED
HumanSP8221833Sp8 transcription factor
INFERRED
HumanFLCN201163folliculin
INFERRED
HumanARL13B200894ADP-ribosylation factor-like 13B
INFERRED
HumanDAND5199699DAN domain family member 5, BMP antagonist
INFERRED
HumanPKD1L1168507polycystic kidney disease 1 like 1
INFERRED
HumanRDH10157506retinol dehydrogenase 10 (all-trans)
INFERRED
HumanAMOT154796angiomotin
Click here to display 136 evidence detail records.
HumanCOMMD1150684copper metabolism (Murr1) domain containing 1
INFERRED
HumanTTBK2146057tau tubulin kinase 2
INFERRED
HumanMESP2145873mesoderm posterior 2 homolog (mouse)
INFERRED
HumanPRICKLE1144165prickle homolog 1 (Drosophila)
INFERRED
HumanRIPPLY2134701ripply transcriptional repressor 2
INFERRED
HumanPIFO128344primary cilia formation
INFERRED
HumanCEP4195681centrosomal protein 41kDa
INFERRED
HumanWNT3A89780wingless-type MMTV integration site family, member 3A
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0002084abnormal developmental patterning0self