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Details
Link-It Detail - Jax Mouse Phenotype - abnormal ependyma motile cilium morphology
Debug Stats
  • ### Total Build Time: 16 ms 20.149 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 412 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 412 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 199 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=2 ms Completed: 2 ms rowSize= 583 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.062 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 1.574 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=7 ms Completed: 7 ms rowSize= 14.621 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.180 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal ependyma motile cilium morphology MP:0011059
Definition (1)
any structural anomaly of the tiny, motile hair-like projections from the epithelial cells that line the ventricles in the brain and the central canal of the spinal cord, which beat in concert and to move cerebrospinal fluid around the central nervous system
Synonyms (1)
"abnormal ependyma motile cilia morphology" EXACT
Parents (1)
img abnormal ependyma morphology MP:0002653
Children (2)
img abnormal spinal cord motile cilium morphology MP:0011058
img abnormal brain ependyma motile cilium morphology MP:0011056
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036315img abnormal ependyma morphology MP:0002653
Genes (12)

Species:
human : 12
SpeciesGeneGeneIdGene NameEvidence
HumanKIF19124602kinesin family member 19
INFERRED
HumanARL684100ADP-ribosylation factor-like 6
INFERRED
HumanCOL18A180781collagen, type XVIII, alpha 1
INFERRED
HumanULK454986unc-51 like kinase 4
INFERRED
HumanMKS154903Meckel syndrome, type 1
img Jax MP, Pubmed Id: 18032602, MOUSE PHENOTYPE ID: MGI:1277215
img Jax MP, Pubmed Id: 23454480, MOUSE PHENOTYPE ID: MGI:3584243
img Jax MP, Pubmed Id: 18250199, MOUSE PHENOTYPE ID: MGI:2389007
img Jax MP, Pubmed Id: 11909969, MOUSE PHENOTYPE ID: MGI:1924407
HumanDPCD25911deleted in primary ciliary dyskinesia homolog (mouse)
img Jax MP, Pubmed Id: 23454480, MOUSE PHENOTYPE ID: MGI:3584243
img Jax MP, Pubmed Id: 18250199, MOUSE PHENOTYPE ID: MGI:2389007
img Jax MP, Pubmed Id: 11909969, MOUSE PHENOTYPE ID: MGI:1924407
img Jax MP, Pubmed Id: 18032602, MOUSE PHENOTYPE ID: MGI:1277215
HumanRFX45992regulatory factor X, 4 (influences HLA class II expression)
INFERRED
HumanPFDN55204prefoldin subunit 5
INFERRED
HumanODF24957outer dense fiber of sperm tails 2
INFERRED
HumanFOXJ12302forkhead box J1
INFERRED
HumanCDC42998cell division cycle 42
INFERRED
HumanBBS1582Bardet-Biedl syndrome 1
img Jax MP, Pubmed Id: 23454480, MOUSE PHENOTYPE ID: MGI:3584243
img Jax MP, Pubmed Id: 18032602, MOUSE PHENOTYPE ID: MGI:1277215
img Jax MP, Pubmed Id: 18250199, MOUSE PHENOTYPE ID: MGI:2389007
img Jax MP, Pubmed Id: 11909969, MOUSE PHENOTYPE ID: MGI:1924407
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0011059abnormal ependyma motile cilium morphology0self