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Details
Link-It Detail - Jax Mouse Phenotype - decreased cochlear hair cell number
Debug Stats
  • ### Total Build Time: 33 ms 68.697 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 398 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 281 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 195 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= 1.032 KB
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.504 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 11.032 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=21 ms Completed: 21 ms rowSize= 52.958 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.173 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
decreased cochlear hair cell number MP:0004408
Definition (1)
decreased number of the sensory epithelial cells of the cochlea, which are normally in synaptic contact with the auditory nerve
Synonyms (1)
"decreased auditory hair cell number" RELATED
Parents (2)
img abnormal cochlear hair cell number MP:0004406
img decreased sensory neuron number MP:0000966
Children (3)
img decreased cochlear outer hair cell number MP:0004402
img absent cochlear hair cells MP:0004405
img decreased cochlear inner hair cell number MP:0004396
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363110img abnormal cochlear hair cell number MP:0004406
img mammalian phenotype MP:0000001img nervous system phenotype MP:000363111img abnormal cochlear hair cell number MP:0004406
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053778img abnormal cochlear hair cell number MP:0004406
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053779img abnormal cochlear hair cell number MP:0004406
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:000537710img abnormal cochlear hair cell number MP:0004406
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:000537711img abnormal cochlear hair cell number MP:0004406
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036318img decreased sensory neuron number MP:0000966
img mammalian phenotype MP:0000001img nervous system phenotype MP:00036317img decreased sensory neuron number MP:0000966
Genes (39)

Species:
human : 39
Page Size
Current 25
  Page 1 of 2
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSLC26A5375611solute carrier family 26 (anion exchanger), member 5
INFERRED
HumanSLC17A8246213solute carrier family 17 (vesicular glutamate transporter), member 8
INFERRED
HumanCYS1192668cystin 1
INFERRED
HumanSRRM484530serine/arginine repetitive matrix 4
INFERRED
HumanTMPRSS364699transmembrane protease, serine 3
INFERRED
HumanCDH2364072cadherin-related 23
img Jax MP, Pubmed Id: 12194867, MOUSE PHENOTYPE ID: MGI:1347464
img Jax MP, Pubmed Id: 21165622, MOUSE PHENOTYPE ID: MGI:2183924
img Jax MP, Pubmed Id: 9668038, MOUSE PHENOTYPE ID: MGI:105368
img Jax MP, Pubmed Id: 22159122, MOUSE PHENOTYPE ID: MGI:96433
img Jax MP
img Jax MP, Pubmed Id: 20502675, MOUSE PHENOTYPE ID: MGI:2682003
img Jax MP, Pubmed Id: 9133426, MOUSE PHENOTYPE ID: MGI:1890219
img Jax MP, Pubmed Id: 17712420, MOUSE PHENOTYPE ID: MGI:1351641
img Jax MP, Pubmed Id: 22235191, MOUSE PHENOTYPE ID: MGI:1891346
img Jax MP, Pubmed Id: 17287518, MOUSE PHENOTYPE ID: MGI:104556
img Jax MP, Pubmed Id: 19363478, MOUSE PHENOTYPE ID: MGI:3619440
HumanHR55806hair growth associated
INFERRED
HumanMYO3A53904myosin IIIA
img Jax MP, Pubmed Id: 22235191, MOUSE PHENOTYPE ID: MGI:1891346
img Jax MP, Pubmed Id: 20502675, MOUSE PHENOTYPE ID: MGI:2682003
img Jax MP, Pubmed Id: 12194867, MOUSE PHENOTYPE ID: MGI:1347464
img Jax MP, Pubmed Id: 22159122, MOUSE PHENOTYPE ID: MGI:96433
img Jax MP, Pubmed Id: 19363478, MOUSE PHENOTYPE ID: MGI:3619440
img Jax MP, Pubmed Id: 17712420, MOUSE PHENOTYPE ID: MGI:1351641
img Jax MP, Pubmed Id: 17287518, MOUSE PHENOTYPE ID: MGI:104556
img Jax MP, Pubmed Id: 21165622, MOUSE PHENOTYPE ID: MGI:2183924
img Jax MP
img Jax MP, Pubmed Id: 9133426, MOUSE PHENOTYPE ID: MGI:1890219
img Jax MP, Pubmed Id: 9668038, MOUSE PHENOTYPE ID: MGI:105368
HumanFGF2026281fibroblast growth factor 20
img Jax MP, Pubmed Id: 12194867, MOUSE PHENOTYPE ID: MGI:1347464
img Jax MP, Pubmed Id: 19363478, MOUSE PHENOTYPE ID: MGI:3619440
img Jax MP, Pubmed Id: 17287518, MOUSE PHENOTYPE ID: MGI:104556
img Jax MP, Pubmed Id: 9668038, MOUSE PHENOTYPE ID: MGI:105368
img Jax MP, Pubmed Id: 20502675, MOUSE PHENOTYPE ID: MGI:2682003
img Jax MP, Pubmed Id: 21165622, MOUSE PHENOTYPE ID: MGI:2183924
img Jax MP
img Jax MP, Pubmed Id: 9133426, MOUSE PHENOTYPE ID: MGI:1890219
img Jax MP, Pubmed Id: 22235191, MOUSE PHENOTYPE ID: MGI:1891346
img Jax MP, Pubmed Id: 17712420, MOUSE PHENOTYPE ID: MGI:1351641
img Jax MP, Pubmed Id: 22159122, MOUSE PHENOTYPE ID: MGI:96433
HumanDFNB3125861deafness, autosomal recessive 31
img Jax MP, Pubmed Id: 22159122, MOUSE PHENOTYPE ID: MGI:96433
img Jax MP, Pubmed Id: 19363478, MOUSE PHENOTYPE ID: MGI:3619440
img Jax MP, Pubmed Id: 9668038, MOUSE PHENOTYPE ID: MGI:105368
img Jax MP
img Jax MP, Pubmed Id: 20502675, MOUSE PHENOTYPE ID: MGI:2682003
img Jax MP, Pubmed Id: 21165622, MOUSE PHENOTYPE ID: MGI:2183924
img Jax MP, Pubmed Id: 17712420, MOUSE PHENOTYPE ID: MGI:1351641
img Jax MP, Pubmed Id: 12194867, MOUSE PHENOTYPE ID: MGI:1347464
img Jax MP, Pubmed Id: 22235191, MOUSE PHENOTYPE ID: MGI:1891346
img Jax MP, Pubmed Id: 9133426, MOUSE PHENOTYPE ID: MGI:1890219
img Jax MP, Pubmed Id: 17287518, MOUSE PHENOTYPE ID: MGI:104556
HumanSLC12A710723solute carrier family 12 (potassium/chloride transporter), member 7
INFERRED
HumanCLDN99080claudin 9
INFERRED
HumanCLRN17401clarin 1
INFERRED
HumanUSH2A7399Usher syndrome 2A (autosomal recessive, mild)
INFERRED
HumanTSHR7253thyroid stimulating hormone receptor
INFERRED
HumanTHRB7068thyroid hormone receptor, beta
INFERRED
HumanSOX26657SRY (sex determining region Y)-box 2
INFERRED
HumanSLC12A26558solute carrier family 12 (sodium/potassium/chloride transporter), member 2
INFERRED
HumanSIX16495SIX homeobox 1
INFERRED
HumanPOU4F35459POU class 4 homeobox 3
INFERRED
HumanNAGLU4669N-acetylglucosaminidase, alpha
img Jax MP, Pubmed Id: 9668038, MOUSE PHENOTYPE ID: MGI:105368
img Jax MP, Pubmed Id: 21165622, MOUSE PHENOTYPE ID: MGI:2183924
img Jax MP, Pubmed Id: 17712420, MOUSE PHENOTYPE ID: MGI:1351641
img Jax MP, Pubmed Id: 12194867, MOUSE PHENOTYPE ID: MGI:1347464
img Jax MP
img Jax MP, Pubmed Id: 22235191, MOUSE PHENOTYPE ID: MGI:1891346
img Jax MP, Pubmed Id: 17287518, MOUSE PHENOTYPE ID: MGI:104556
img Jax MP, Pubmed Id: 19363478, MOUSE PHENOTYPE ID: MGI:3619440
img Jax MP, Pubmed Id: 20502675, MOUSE PHENOTYPE ID: MGI:2682003
img Jax MP, Pubmed Id: 9133426, MOUSE PHENOTYPE ID: MGI:1890219
img Jax MP, Pubmed Id: 22159122, MOUSE PHENOTYPE ID: MGI:96433
HumanMYO7A4647myosin VIIA
INFERRED
HumanLFNG3955LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
INFERRED
HumanLAMA23908laminin, alpha 2
INFERRED
HumanKCNE13753potassium voltage-gated channel, Isk-related family, member 1
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0004408decreased cochlear hair cell number0self