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Details
Link-It Detail - Jax Mouse Phenotype - abnormal dosage compensation, by inactivation of X chromosome
Debug Stats
  • ### Total Build Time: 27 ms 37.136 KB
  • CONCEPT_NAME gt=12 ms Completed: 12 ms rowSize= 450 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 362 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 192 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=3 ms Completed: 3 ms rowSize= 583 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 1.568 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=8 ms Completed: 8 ms rowSize= 32.667 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.198 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal dosage compensation, by inactivation of X chromosome MP:0010382
Definition (1)
anomaly in the process of compensating for the two-fold variation in X-chromosome:autosome ratios between sexes by a global inactivation of all, or most of, the genes on one of the X-chromosomes in the XX sex
Synonyms (1)
"abnormal X chromosome inactivation" EXACT
Parents (1)
img abnormal dosage compensation MP:0010381
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img cellular phenotype MP:00053845img abnormal dosage compensation MP:0010381
Genes (3)

Species:
human : 3
SpeciesGeneGeneIdGene NameEvidence
HumanRLIM51132ring finger protein, LIM domain interacting
img Jax MP, Pubmed Id: 10520993, MOUSE PHENOTYPE ID: MGI:1336196
img Jax MP, Pubmed Id: 21389056, MOUSE PHENOTYPE ID: MGI:3055028
img Jax MP, Pubmed Id: 20962847, MOUSE PHENOTYPE ID: MGI:1342291
img Jax MP, Pubmed Id: 21852535, MOUSE PHENOTYPE ID: MGI:104735
img Jax MP, Pubmed Id: 15668296, MOUSE PHENOTYPE ID: MGI:98974
img Jax MP, Pubmed Id: 16549272, MOUSE PHENOTYPE ID: MGI:99918
img Jax MP, Pubmed Id: 12952890, MOUSE PHENOTYPE ID: MGI:98974
img Jax MP, Pubmed Id: 15668296, MOUSE PHENOTYPE ID: MGI:98974
img Jax MP, Pubmed Id: 12952890, MOUSE PHENOTYPE ID: MGI:98974
img Jax MP, Pubmed Id: 12930754, MOUSE PHENOTYPE ID: MGI:3043979
img Jax MP, Pubmed Id: 22606329, MOUSE PHENOTYPE ID: MGI:1919834
img Jax MP, Pubmed Id: 21389056, MOUSE PHENOTYPE ID: MGI:98974
img Jax MP, Pubmed Id: 12952890, MOUSE PHENOTYPE ID: MGI:98974
img Jax MP, Pubmed Id: 10520993, MOUSE PHENOTYPE ID: MGI:1336196
HumanCUL4B8450cullin 4B
img Jax MP, Pubmed Id: 15668296, MOUSE PHENOTYPE ID: MGI:98974
img Jax MP, Pubmed Id: 21389056, MOUSE PHENOTYPE ID: MGI:3055028
img Jax MP, Pubmed Id: 20962847, MOUSE PHENOTYPE ID: MGI:1342291
img Jax MP, Pubmed Id: 21389056, MOUSE PHENOTYPE ID: MGI:98974
img Jax MP, Pubmed Id: 10520993, MOUSE PHENOTYPE ID: MGI:1336196
img Jax MP, Pubmed Id: 12952890, MOUSE PHENOTYPE ID: MGI:98974
img Jax MP, Pubmed Id: 21852535, MOUSE PHENOTYPE ID: MGI:104735
img Jax MP, Pubmed Id: 12952890, MOUSE PHENOTYPE ID: MGI:98974
img Jax MP, Pubmed Id: 12952890, MOUSE PHENOTYPE ID: MGI:98974
img Jax MP, Pubmed Id: 10520993, MOUSE PHENOTYPE ID: MGI:1336196
img Jax MP, Pubmed Id: 12930754, MOUSE PHENOTYPE ID: MGI:3043979
img Jax MP, Pubmed Id: 15668296, MOUSE PHENOTYPE ID: MGI:98974
img Jax MP, Pubmed Id: 22606329, MOUSE PHENOTYPE ID: MGI:1919834
img Jax MP, Pubmed Id: 16549272, MOUSE PHENOTYPE ID: MGI:99918
HumanMECP24204methyl CpG binding protein 2 (Rett syndrome)
img Jax MP, Pubmed Id: 12952890, MOUSE PHENOTYPE ID: MGI:98974
img Jax MP, Pubmed Id: 12952890, MOUSE PHENOTYPE ID: MGI:98974
img Jax MP, Pubmed Id: 10520993, MOUSE PHENOTYPE ID: MGI:1336196
img Jax MP, Pubmed Id: 10520993, MOUSE PHENOTYPE ID: MGI:1336196
img Jax MP, Pubmed Id: 15668296, MOUSE PHENOTYPE ID: MGI:98974
img Jax MP, Pubmed Id: 21852535, MOUSE PHENOTYPE ID: MGI:104735
img Jax MP, Pubmed Id: 12930754, MOUSE PHENOTYPE ID: MGI:3043979
img Jax MP, Pubmed Id: 21389056, MOUSE PHENOTYPE ID: MGI:98974
img Jax MP, Pubmed Id: 16549272, MOUSE PHENOTYPE ID: MGI:99918
img Jax MP, Pubmed Id: 12952890, MOUSE PHENOTYPE ID: MGI:98974
img Jax MP, Pubmed Id: 21389056, MOUSE PHENOTYPE ID: MGI:3055028
img Jax MP, Pubmed Id: 20962847, MOUSE PHENOTYPE ID: MGI:1342291
img Jax MP, Pubmed Id: 15668296, MOUSE PHENOTYPE ID: MGI:98974
img Jax MP, Pubmed Id: 22606329, MOUSE PHENOTYPE ID: MGI:1919834
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0010382abnormal dosage compensation, by inactivation of X chromosome0self