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Details
Link-It Detail - Jax Mouse Phenotype - abnormal gastrulation
Debug Stats
  • ### Total Build Time: 328 ms 21.099 KB
  • CONCEPT_NAME gt=14 ms Completed: 14 ms rowSize= 370 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 230 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=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=3 ms Completed: 3 ms rowSize= 588 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.472 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.578 KB
  • CONCEPT_RELATIONSHIPS gt=2 ms Completed: 2 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=303 ms Completed: 303 ms rowSize= 15.585 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.159 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal gastrulation MP:0001695
Definition (1)
any anomaly in the development and invagination of the embryonic germ layers
Parents (1)
img abnormal developmental patterning MP:0002084
Children (3)
img abnormal gastrulation movements MP:0002174
img abnormal embryo turning MP:0001700
img failure to gastrulate MP:0001696
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img embryogenesis phenotype MP:00053805img abnormal developmental patterning MP:0002084
Genes (240)

Species:
human : 240
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SpeciesGeneGeneIdGene NameEvidence
HumanSCXA100129885scleraxis homolog A (mouse)
INFERRED
HumanCFC1B653275cripto, FRL-1, cryptic family 1B
INFERRED
HumanSCXB642658scleraxis homolog B (mouse)
INFERRED
HumanCRB2286204crumbs homolog 2 (Drosophila)
INFERRED
HumanDPH3285381diphthamide biosynthesis 3
INFERRED
HumanLAMA1284217laminin, alpha 1
Click here to display 88 evidence detail records.
HumanIPMK253430inositol polyphosphate multikinase
INFERRED
HumanPKD1L1168507polycystic kidney disease 1 like 1
INFERRED
HumanRDH10157506retinol dehydrogenase 10 (all-trans)
INFERRED
HumanCOMMD1150684copper metabolism (Murr1) domain containing 1
INFERRED
HumanTTBK2146057tau tubulin kinase 2
INFERRED
HumanMESP2145873mesoderm posterior 2 homolog (mouse)
Click here to display 88 evidence detail records.
HumanCEP4195681centrosomal protein 41kDa
INFERRED
HumanWNT3A89780wingless-type MMTV integration site family, member 3A
Click here to display 88 evidence detail records.
HumanDISP184976dispatched homolog 1 (Drosophila)
INFERRED
HumanATAD3B83858ATPase family, AAA domain containing 3B
INFERRED
HumanKDM879831lysine (K)-specific demethylase 8
INFERRED
HumanPALB279728partner and localizer of BRCA2
Click here to display 88 evidence detail records.
HumanSRD5A379644steroid 5 alpha-reductase 3
INFERRED
HumanSMURF264750SMAD specific E3 ubiquitin protein ligase 2
Click here to display 88 evidence detail records.
HumanNSD164324nuclear receptor binding SET domain protein 1
INFERRED
HumanSOX1764321SRY (sex determining region Y)-box 17
INFERRED
HumanEXOC460412exocyst complex component 4
Click here to display 88 evidence detail records.
HumanOVOL258495ovo-like 2 (Drosophila)
INFERRED
HumanGRHL357822grainyhead-like 3 (Drosophila)
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001695abnormal gastrulation0self