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Details
Link-It Detail - Jax Mouse Phenotype - impaired somite development
Debug Stats
  • ### Total Build Time: 101 ms 20.058 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 382 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 257 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=11 ms Completed: 11 ms rowSize= 582 bytes
  • CONCEPT_CHILDREN gt=9 ms Completed: 9 ms rowSize= 1.029 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=8 ms Completed: 8 ms rowSize= 1.572 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=63 ms Completed: 63 ms rowSize= 14.954 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.165 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
impaired somite development MP:0009768
Definition (1)
atypical process of somite formation with the result of fewer or none of these cell masses being formed
Parents (1)
img abnormal somite development MP:0001688
Children (2)
img incomplete somite formation MP:0001689
img failure of somite differentiation MP:0001690
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img embryogenesis phenotype MP:00053806img abnormal somite development MP:0001688
Genes (94)

Species:
human : 94
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSCXA100129885scleraxis homolog A (mouse)
INFERRED
HumanSCXB642658scleraxis homolog B (mouse)
INFERRED
HumanNRARP441478NOTCH-regulated ankyrin repeat protein
INFERRED
HumanMSGN1343930mesogenin 1
INFERRED
HumanMESP2145873mesoderm posterior 2 homolog (mouse)
INFERRED
HumanRAD9B144715RAD9 homolog B (S. pombe)
Click here to display 21 evidence detail records.
HumanRIPPLY2134701ripply transcriptional repressor 2
INFERRED
HumanWNT3A89780wingless-type MMTV integration site family, member 3A
INFERRED
HumanHES784667hairy and enhancer of split 7 (Drosophila)
INFERRED
HumanEHMT179813euchromatic histone-lysine N-methyltransferase 1
INFERRED
HumanPALB279728partner and localizer of BRCA2
INFERRED
HumanRNASEH2B79621ribonuclease H2, subunit B
Click here to display 21 evidence detail records.
HumanEPB41L557669erythrocyte membrane protein band 4.1 like 5
INFERRED
HumanWDR3557539WD repeat domain 35
Click here to display 21 evidence detail records.
HumanMIB157534mindbomb E3 ubiquitin protein ligase 1
INFERRED
HumanPOGLUT156983protein O-glucosyltransferase 1
INFERRED
HumanMESP155897mesoderm posterior 1 homolog (mouse)
INFERRED
HumanSUPT20H55578suppressor of Ty 20 homolog (S. cerevisiae)
INFERRED
HumanRRN354700RRN3 RNA polymerase I transcription factor homolog (S. cerevisiae)
INFERRED
HumanDACT151339dishevelled-binding antagonist of beta-catenin 1
Click here to display 21 evidence detail records.
HumanLEF151176lymphoid enhancer-binding factor 1
INFERRED
HumanHSD17B1251144hydroxysteroid (17-beta) dehydrogenase 12
INFERRED
HumanEPN129924epsin 1
INFERRED
HumanDLL128514delta-like 1 (Drosophila)
INFERRED
HumanTENM426011teneurin transmembrane protein 4
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0009768impaired somite development0self