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Details
Link-It Detail - Jax Mouse Phenotype - sensorineural hearing impairment
Debug Stats
  • ### Total Build Time: 26 ms 18.973 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 392 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 262 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 189 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= 571 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 583 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.570 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=13 ms Completed: 13 ms rowSize= 14.138 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.170 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
sensorineural hearing impairment MP:0006329
Definition (1)
a form of hearing impairment due to a lesion of the auditory division of cranial nerve VIII or the inner ear
Synonyms (1)
"perceptive hearing impairment" RELATED
Parents (1)
img impaired hearing MP:0006325
Children (1)
img sensorineural hearing loss MP:0004740
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053776img impaired hearing MP:0006325
Genes (28)

Species:
human : 28
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSLC17A8246213solute carrier family 17 (vesicular glutamate transporter), member 8
INFERRED
HumanGJB610804gap junction protein, beta 6, 30kDa
INFERRED
HumanSLC19A210560solute carrier family 19 (thiamine transporter), member 2
INFERRED
HumanSLC12A69990solute carrier family 12 (potassium/chloride transporter), member 6
INFERRED
HumanLARGE9215like-glycosyltransferase
INFERRED
HumanKCNQ49132potassium voltage-gated channel, KQT-like subfamily, member 4
INFERRED
HumanSYNJ28871synaptojanin 2
INFERRED
HumanTHRB7068thyroid hormone receptor, beta
INFERRED
HumanPSAP5660prosaposin
INFERRED
HumanPOU3F45456POU class 3 homeobox 4
INFERRED
HumanSLC26A45172solute carrier family 26 (anion exchanger), member 4
INFERRED
HumanNGFR4804nerve growth factor receptor
INFERRED
HumanNDP4693Norrie disease (pseudoglioma)
INFERRED
HumanKCNMA13778potassium large conductance calcium-activated channel, subfamily M, alpha member 1
INFERRED
HumanIGF13479insulin-like growth factor 1 (somatomedin C)
INFERRED
HumanIDUA3425iduronidase, alpha-L-
INFERRED
HumanGATA32625GATA binding protein 3
INFERRED
HumanGABRB32562gamma-aminobutyric acid (GABA) A receptor, beta 3
INFERRED
HumanGABRB22561gamma-aminobutyric acid (GABA) A receptor, beta 2
INFERRED
HumanGABRA52558gamma-aminobutyric acid (GABA) A receptor, alpha 5
INFERRED
HumanFGFR32261fibroblast growth factor receptor 3
INFERRED
HumanCOL11A21302collagen, type XI, alpha 2
INFERRED
HumanCOL4A41286collagen, type IV, alpha 4
INFERRED
HumanCOL4A31285collagen, type IV, alpha 3 (Goodpasture antigen)
INFERRED
HumanCDKN2D1032cyclin-dependent kinase inhibitor 2D (p19, inhibits CDK4)
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0006329sensorineural hearing impairment0self