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Details
Link-It Detail - Jax Mouse Phenotype - abnormal cochlear outer hair cell morphology
Debug Stats
  • ### Total Build Time: 127 ms 30.155 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 416 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
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  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 180 bytes
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  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 3.396 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 8.367 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=109 ms Completed: 109 ms rowSize= 15.284 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.182 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal cochlear outer hair cell morphology MP:0004399
Definition (1)
any structural anomaly in the sensory cells of the organ of Corti which are in synaptic contact with sensory as well as efferent fibers of the auditory nerve; there are three rows of columnar outer hair cells largely surrounded by cortilymph and supporting phalangeal cells; the apical end of each cell is anchored to the cuticular plate and about 100 stereocilia arranged in a V-shaped pattern extend from the cell's surface through the cuticular plate into the tectorial membrane
Synonyms (1)
"abnormal cochlear OHCs" EXACT
Parents (1)
img abnormal cochlear hair cell morphology MP:0002622
Children (7)
img abnormal cochlear OHC efferent innervation pattern MP:0004632
img short cochlear outer hair cells MP:0004466
img abnormal cochlear OHC afferent innervation pattern MP:0004747
img absent cochlear outer hair cells MP:0004403
img cochlear outer hair cell degeneration MP:0004404
img abnormal cochlear outer hair cell number MP:0004400
img abnormal outer hair cell stereociliary bundle morphology MP:0004527
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036319img abnormal cochlear hair cell morphology MP:0002622
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363110img abnormal cochlear hair cell morphology MP:0002622
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053777img abnormal cochlear hair cell morphology MP:0002622
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053778img abnormal cochlear hair cell morphology MP:0002622
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053779img abnormal cochlear hair cell morphology MP:0002622
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:000537710img abnormal cochlear hair cell morphology MP:0002622
Genes (118)

Species:
human : 118
Page Size
Current 25
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SpeciesGeneGeneIdGene NameEvidence
HumanGRXCR1389207glutaredoxin, cysteine rich 1
INFERRED
HumanHES5388585hairy and enhancer of split 5 (Drosophila)
INFERRED
HumanSLC26A5375611solute carrier family 26 (anion exchanger), member 5
Click here to display 50 evidence detail records.
HumanPTPRQ374462protein tyrosine phosphatase, receptor type, Q
INFERRED
HumanLHFPL5222662lipoma HMGIC fusion partner-like 5
INFERRED
HumanLRTOMT220074leucine rich transmembrane and O-methyltransferase domain containing
INFERRED
HumanCYS1192668cystin 1
INFERRED
HumanSYNE4163183spectrin repeat containing, nuclear envelope family member 4
Click here to display 50 evidence detail records.
HumanSTRC161497stereocilin
INFERRED
HumanUSH1G124590Usher syndrome 1G (autosomal recessive)
INFERRED
HumanTMC1117531transmembrane channel-like 1
INFERRED
HumanSLITRK684189SLIT and NTRK-like family, member 6
INFERRED
HumanGPR9884059G protein-coupled receptor 98
INFERRED
HumanESPN83715espin
INFERRED
HumanFAT479633FAT atypical cadherin 4
INFERRED
HumanSMURF264750SMAD specific E3 ubiquitin protein ligase 2
INFERRED
HumanTMPRSS364699transmembrane protease, serine 3
INFERRED
HumanCDH2364072cadherin-related 23
Click here to display 50 evidence detail records.
HumanVANGL257216VANGL planar cell polarity protein 2
Click here to display 50 evidence detail records.
HumanCHRNA1057053cholinergic receptor, nicotinic, alpha 10 (neuronal)
INFERRED
HumanBARHL156751BarH-like homeobox 1
INFERRED
HumanHR55806hair growth associated
INFERRED
HumanCHD755636chromodomain helicase DNA binding protein 7
INFERRED
HumanCHRNA955584cholinergic receptor, nicotinic, alpha 9 (neuronal)
INFERRED
HumanMKS154903Meckel syndrome, type 1
Click here to display 50 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004399abnormal cochlear outer hair cell morphology0self