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Details
Link-It Detail - Jax Mouse Phenotype - abnormal cochlear outer hair cell number
Debug Stats
  • ### Total Build Time: 24 ms 26.089 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 408 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 232 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=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= 599 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.051 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 8.404 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=13 ms Completed: 13 ms rowSize= 13.908 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.178 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
abnormal cochlear outer hair cell number MP:0004400
Definition (1)
abnormal number of the columnar outer hair sensory cells of the organ of Corti
Synonyms (1)
"abnormal auditory outer hair cell number" EXACT
Parents (1)
img abnormal cochlear outer hair cell morphology MP:0004399
Children (2)
img increased cochlear outer hair cell number MP:0004401
img decreased cochlear outer hair cell number MP:0004402
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363110img abnormal cochlear outer hair cell morphology MP:0004399
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363111img abnormal cochlear outer hair cell morphology MP:0004399
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053778img abnormal cochlear outer hair cell morphology MP:0004399
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053779img abnormal cochlear outer hair cell morphology MP:0004399
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:000537710img abnormal cochlear outer hair cell morphology MP:0004399
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:000537711img abnormal cochlear outer hair cell morphology MP:0004399
Genes (43)

Species:
human : 43
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanHES5388585hairy and enhancer of split 5 (Drosophila)
INFERRED
HumanSLC26A5375611solute carrier family 26 (anion exchanger), member 5
INFERRED
HumanCYS1192668cystin 1
INFERRED
HumanTMPRSS364699transmembrane protease, serine 3
INFERRED
HumanCDH2364072cadherin-related 23
INFERRED
HumanVANGL257216VANGL planar cell polarity protein 2
INFERRED
HumanHR55806hair growth associated
INFERRED
HumanCHD755636chromodomain helicase DNA binding protein 7
INFERRED
HumanMYO3A53904myosin IIIA
INFERRED
HumanDLL128514delta-like 1 (Drosophila)
INFERRED
HumanFGF2026281fibroblast growth factor 20
INFERRED
HumanSLC12A710723solute carrier family 12 (potassium/chloride transporter), member 7
INFERRED
HumanSPRY210253sprouty homolog 2 (Drosophila)
INFERRED
HumanNOG9241noggin
INFERRED
HumanCLDN99080claudin 9
INFERRED
HumanCLRN17401clarin 1
INFERRED
HumanUSH2A7399Usher syndrome 2A (autosomal recessive, mild)
INFERRED
HumanTSHR7253thyroid stimulating hormone receptor
INFERRED
HumanTHRB7068thyroid hormone receptor, beta
INFERRED
HumanNR2F17025nuclear receptor subfamily 2, group F, member 1
INFERRED
HumanSLC12A26558solute carrier family 12 (sodium/potassium/chloride transporter), member 2
INFERRED
HumanPTK75754protein tyrosine kinase 7
INFERRED
HumanNOTCH14851notch 1
INFERRED
HumanMYO7A4647myosin VIIA
INFERRED
HumanLFNG3955LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004400abnormal cochlear outer hair cell number0self