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Details
Link-It Detail - Jax Mouse Phenotype - impaired hearing
Debug Stats
  • ### Total Build Time: 582 ms 24.110 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 360 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 198 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 172 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=11 ms Completed: 11 ms rowSize= 582 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 3.274 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=5 ms Completed: 5 ms rowSize= 1.581 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=551 ms Completed: 551 ms rowSize= 16.675 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.154 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
impaired hearing MP:0006325
Definition (1)
reduced ability to perceive auditory stimuli
Synonyms (1)
"hearing loss" RELATED
Parents (1)
img abnormal hearing physiology MP:0001963
Children (7)
img unilateral deafness MP:0004699
img deafness MP:0001967
img mixed hearing impairment MP:0006327
img sensorineural hearing impairment MP:0006329
img conductive hearing impairment MP:0006326
img nonsyndromic hearing impairment MP:0006328
img syndromic hearing impairment MP:0006330
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053775img abnormal hearing physiology MP:0001963
Genes (135)

Species:
human : 135
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanGRXCR1389207glutaredoxin, cysteine rich 1
Click here to display 142 evidence detail records.
HumanCEACAM16388551carcinoembryonic antigen-related cell adhesion molecule 16
INFERRED
HumanSLC26A5375611solute carrier family 26 (anion exchanger), member 5
Click here to display 142 evidence detail records.
HumanPTPRQ374462protein tyrosine phosphatase, receptor type, Q
INFERRED
HumanOTOG340990otogelin
Click here to display 142 evidence detail records.
HumanTMIE259236transmembrane inner ear
INFERRED
HumanSLC17A8246213solute carrier family 17 (vesicular glutamate transporter), member 8
INFERRED
HumanLHFPL5222662lipoma HMGIC fusion partner-like 5
INFERRED
HumanLRTOMT220074leucine rich transmembrane and O-methyltransferase domain containing
INFERRED
HumanSTRC161497stereocilin
Click here to display 142 evidence detail records.
HumanOTOS150677otospiralin
INFERRED
HumanOTOA146183otoancorin
Click here to display 142 evidence detail records.
HumanUSH1G124590Usher syndrome 1G (autosomal recessive)
INFERRED
HumanTMC1117531transmembrane channel-like 1
Click here to display 142 evidence detail records.
HumanGPR9884059G protein-coupled receptor 98
INFERRED
HumanSLC4A1183959solute carrier family 4, sodium borate transporter, member 11
Click here to display 142 evidence detail records.
HumanESPN83715espin
INFERRED
HumanDNAJC580331DnaJ (Hsp40) homolog, subfamily C, member 5
Click here to display 142 evidence detail records.
HumanFBXO1180204F-box protein 11
Click here to display 142 evidence detail records.
HumanTMPRSS364699transmembrane protease, serine 3
INFERRED
HumanCDH2364072cadherin-related 23
Click here to display 142 evidence detail records.
HumanTRPV459341transient receptor potential cation channel, subfamily V, member 4
Click here to display 142 evidence detail records.
HumanSALL457167sal-like 4 (Drosophila)
Click here to display 142 evidence detail records.
HumanFAM20C56975family with sequence similarity 20, member C
Click here to display 142 evidence detail records.
HumanBARHL156751BarH-like homeobox 1
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0006325impaired hearing0self