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Details
Link-It Detail - Jax Mouse Phenotype - complete lethality throughout fetal growth and development
Debug Stats
  • ### Total Build Time: 3,950 ms 23.569 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 444 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 296 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=2 ms Completed: 2 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 604 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 2.938 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=3,935 ms Completed: 3.935 Seconds rowSize= 17.972 KB
  • CONCEPT_XREFS gt=6 ms Completed: 6 ms rowSize= 1.195 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
complete lethality throughout fetal growth and development MP:0011099
Definition (1)
death of all organisms of a given genotype in a population between the completion of organogenesis and birth (Mus: E14 to approximately E18.5)
Parents (1)
img lethality throughout fetal growth and development MP:0006208
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img mortality/aging MP:00107687img lethality throughout fetal growth and development MP:0006208
img mammalian phenotype MP:0000001img mortality/aging MP:00107686img lethality throughout fetal growth and development MP:0006208
Genes (227)

Species:
human : 227
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Current 25
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SpeciesGeneGeneIdGene NameEvidence
HumanRICTOR253260RPTOR independent companion of MTOR, complex 2
Click here to display 380 evidence detail records.
HumanPKD1L1168507polycystic kidney disease 1 like 1
Click here to display 380 evidence detail records.
HumanPHOSPHO1162466phosphatase, orphan 1
Click here to display 380 evidence detail records.
HumanZFPM1161882zinc finger protein, FOG family member 1
Click here to display 380 evidence detail records.
HumanGATA5140628GATA binding protein 5
Click here to display 380 evidence detail records.
HumanTRIM71131405tripartite motif containing 71, E3 ubiquitin protein ligase
Click here to display 380 evidence detail records.
HumanOSR1130497odd-skipped related 1 (Drosophila)
Click here to display 380 evidence detail records.
HumanTWIST2117581twist basic helix-loop-helix transcription factor 2
Click here to display 380 evidence detail records.
HumanFUZ80199fuzzy planar cell polarity protein
Click here to display 380 evidence detail records.
HumanFRAS180144Fraser syndrome 1
Click here to display 380 evidence detail records.
HumanGRHL279977grainyhead-like 2 (Drosophila)
Click here to display 380 evidence detail records.
HumanMYH1479784myosin, heavy chain 14, non-muscle
Click here to display 380 evidence detail records.
HumanTCTN179600tectonic family member 1
Click here to display 380 evidence detail records.
HumanTMEM23179583transmembrane protein 231
Click here to display 380 evidence detail records.
HumanIRX379191iroquois homeobox 3
Click here to display 380 evidence detail records.
HumanPORCN64840porcupine homolog (Drosophila)
Click here to display 380 evidence detail records.
HumanNEUROD458158neuronal differentiation 4
Click here to display 380 evidence detail records.
HumanWDR1957728WD repeat domain 19
Click here to display 380 evidence detail records.
HumanMKL257496MKL/myocardin-like 2
Click here to display 380 evidence detail records.
HumanC1GALT156913core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1
Click here to display 380 evidence detail records.
HumanPARVA55742parvin, alpha
Click here to display 380 evidence detail records.
HumanAMBRA155626autophagy/beclin-1 regulator 1
Click here to display 380 evidence detail records.
HumanPBRM155193polybromo 1
Click here to display 380 evidence detail records.
HumanMKS154903Meckel syndrome, type 1
Click here to display 380 evidence detail records.
HumanSOX1854345SRY (sex determining region Y)-box 18
Click here to display 380 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0011099complete lethality throughout fetal growth and development0self