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Details
Link-It Detail - Jax Mouse Phenotype - abnormal somite development
Debug Stats
  • ### Total Build Time: 1,646 ms 24.788 KB
  • CONCEPT_NAME gt=6 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= 281 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 198 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=6 ms Completed: 6 ms rowSize= 591 bytes
  • CONCEPT_CHILDREN gt=24 ms Completed: 24 ms rowSize= 3.781 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.581 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=1,597 ms Completed: 1.597 Seconds rowSize= 16.698 KB
  • CONCEPT_XREFS gt=10 ms Completed: 10 ms rowSize= 1.165 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal somite development MP:0001688
Definition (1)
any anomaly in the formation of any of the paired, metamerically arranged cell masses formed in the embryonic paraxial mesoderm
Synonyms (1)
"abnormal metablastic segment development" EXACT
Parents (1)
img abnormal embryonic tissue morphology MP:0002085
Children (8)
img abnormal left-right axis symmetry of the somites MP:0005224
img abnormal somite shape MP:0001691
img impaired somite development MP:0009768
img abnormal anterior-posterior polarity of the somites MP:0005223
img abnormal somite size MP:0005222
img fused somites MP:0011733
img delayed somite formation MP:0003794
img abnormal rostral-caudal patterning of the somites MP:0008530
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img embryogenesis phenotype MP:00053805img abnormal embryonic tissue morphology MP:0002085
Genes (196)

Species:
human : 196
Page Size
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SpeciesGeneGeneIdGene NameEvidence
HumanCOMMD3-BMI1100532731
Click here to display 188 evidence detail records.
HumanSCXA100129885scleraxis homolog A (mouse)
INFERRED
HumanSCXB642658scleraxis homolog B (mouse)
INFERRED
HumanNRARP441478NOTCH-regulated ankyrin repeat protein
Click here to display 188 evidence detail records.
HumanEVX2344191even-skipped homeobox 2
Click here to display 188 evidence detail records.
HumanNOTO344022notochord homeobox
Click here to display 188 evidence detail records.
HumanMSGN1343930mesogenin 1
INFERRED
HumanCRB2286204crumbs homolog 2 (Drosophila)
Click here to display 188 evidence detail records.
HumanRDH10157506retinol dehydrogenase 10 (all-trans)
INFERRED
HumanMESP2145873mesoderm posterior 2 homolog (mouse)
Click here to display 188 evidence detail records.
HumanRAD9B144715RAD9 homolog B (S. pombe)
INFERRED
HumanRIPPLY2134701ripply transcriptional repressor 2
INFERRED
HumanWNT3A89780wingless-type MMTV integration site family, member 3A
Click here to display 188 evidence detail records.
HumanDISP184976dispatched homolog 1 (Drosophila)
Click here to display 188 evidence detail records.
HumanHES784667hairy and enhancer of split 7 (Drosophila)
Click here to display 188 evidence detail records.
HumanMIXL183881Mix paired-like homeobox
Click here to display 188 evidence detail records.
HumanCCM283605cerebral cavernous malformation 2
Click here to display 188 evidence detail records.
HumanTCF7L183439transcription factor 7-like 1 (T-cell specific, HMG-box)
Click here to display 188 evidence detail records.
HumanAMN81693amnion associated transmembrane protein
Click here to display 188 evidence detail records.
HumanEHMT179813euchromatic histone-lysine N-methyltransferase 1
INFERRED
HumanPALB279728partner and localizer of BRCA2
INFERRED
HumanRNASEH2B79621ribonuclease H2, subunit B
INFERRED
HumanWDR1957728WD repeat domain 19
Click here to display 188 evidence detail records.
HumanEPB41L557669erythrocyte membrane protein band 4.1 like 5
Click here to display 188 evidence detail records.
HumanWDR3557539WD repeat domain 35
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001688abnormal somite development0self