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Details
Link-It Detail - Jax Mouse Phenotype - conductive hearing impairment
Debug Stats
  • ### Total Build Time: 64 ms 11.510 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 386 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 246 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 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=12 ms Completed: 12 ms rowSize= 571 bytes
  • CONCEPT_CHILDREN gt=10 ms Completed: 10 ms rowSize= 580 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=9 ms Completed: 9 ms rowSize= 1.570 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=22 ms Completed: 22 ms rowSize= 6.887 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.167 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Jax Mouse Phenotype (1)
conductive hearing impairment MP:0006326
Definition (1)
reduction in the ability to hear due to lesions in the external auditory canal or middle ear
Parents (1)
img impaired hearing MP:0006325
Children (1)
img conductive hearing loss MP:0004739
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053776img impaired hearing MP:0006325
Genes (11)

Species:
human : 11
SpeciesGeneGeneIdGene NameEvidence
HumanDNAJC580331DnaJ (Hsp40) homolog, subfamily C, member 5
img Jax MP, Pubmed Id: 17523175, MOUSE PHENOTYPE ID: MGI:2447280
img Jax MP, Pubmed Id: 16477021, MOUSE PHENOTYPE ID: MGI:892995
HumanSALL457167sal-like 4 (Drosophila)
INFERRED
HumanNOG9241noggin
INFERRED
HumanTFAP2A7020transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
INFERRED
HumanSIX16495SIX homeobox 1
INFERRED
HumanSALL16299sal-like 1 (Drosophila)
INFERRED
HumanRPL386169ribosomal protein L38
INFERRED
HumanPOU3F45456POU class 3 homeobox 4
INFERRED
HumanNAGLU4669N-acetylglucosaminidase, alpha
INFERRED
HumanEYA12138eyes absent homolog 1 (Drosophila)
INFERRED
HumanDLX11745distal-less homeobox 1
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0006326conductive hearing impairment0self