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Details
Link-It Detail - Jax Mouse Phenotype - abnormal kinocilium morphology
Debug Stats
  • ### Total Build Time: 26 ms 16.452 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 388 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 271 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 187 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=6 ms Completed: 6 ms rowSize= 584 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.538 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 4.266 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=14 ms Completed: 14 ms rowSize= 7.939 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.168 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal kinocilium morphology MP:0011060
Definition (1)
any structural anomaly of the nonmotile primary cilium that is found at the apical surface of auditory receptor cells
Synonyms (1)
"abnormal kinocilia morphology" EXACT
Parents (1)
img abnormal hair cell morphology MP:0000045
Children (3)
img abnormal vestibular hair cell kinocilium morphology MP:0011064
img abnormal inner hair cell kinocilium morphology MP:0011061
img abnormal outer hair cell kinocilium morphology MP:0011062
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036318img abnormal hair cell morphology MP:0000045
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036319img abnormal hair cell morphology MP:0000045
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053776img abnormal hair cell morphology MP:0000045
Genes (10)

Species:
human : 10
SpeciesGeneGeneIdGene NameEvidence
HumanGRXCR1389207glutaredoxin, cysteine rich 1
INFERRED
HumanUSH1G124590Usher syndrome 1G (autosomal recessive)
INFERRED
HumanTMPRSS364699transmembrane protease, serine 3
img Jax MP, Pubmed Id: 21454591, MOUSE PHENOTYPE ID: MGI:2155445
img Jax MP, Pubmed Id: 14981357, MOUSE PHENOTYPE ID: MGI:97492
HumanCDH2364072cadherin-related 23
INFERRED
HumanCELSR19620cadherin, EGF LAG seven-pass G-type receptor 1
INFERRED
HumanMKKS8195McKusick-Kaufman syndrome
INFERRED
HumanPAX87849paired box 8
img Jax MP, Pubmed Id: 14981357, MOUSE PHENOTYPE ID: MGI:97492
img Jax MP, Pubmed Id: 21454591, MOUSE PHENOTYPE ID: MGI:2155445
HumanPTK75754protein tyrosine kinase 7
INFERRED
HumanIGF1R3480insulin-like growth factor 1 receptor
INFERRED
HumanFGF102255fibroblast growth factor 10
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0011060abnormal kinocilium morphology0self