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Details
Link-It Detail - Jax Mouse Phenotype - abnormal incus morphology
Debug Stats
  • ### Total Build Time: 43 ms 21.908 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 378 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 221 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=6 ms Completed: 6 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 593 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 569 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 4.284 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=29 ms Completed: 29 ms rowSize= 14.597 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.163 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal incus morphology MP:0005106
Definition (1)
any structural anomaly of the middle of the three auditory ossicles
Parents (1)
img abnormal middle ear ossicle morphology MP:0005105
Children (1)
img absent incus MP:0004318
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img craniofacial phenotype MP:00053826img abnormal middle ear ossicle morphology MP:0005105
img mammalian phenotype MP:0000001img skeleton phenotype MP:00053907img abnormal middle ear ossicle morphology MP:0005105
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053776img abnormal middle ear ossicle morphology MP:0005105
Genes (25)

Species:
human : 25
SpeciesGeneGeneIdGene NameEvidence
HumanGDF6392255growth differentiation factor 6
Click here to display 35 evidence detail records.
HumanANKH56172ANKH inorganic pyrophosphate transport regulator
Click here to display 35 evidence detail records.
HumanCHD755636chromodomain helicase DNA binding protein 7
Click here to display 35 evidence detail records.
HumanNOG9241noggin
Click here to display 35 evidence detail records.
HumanTFAP2A7020transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
Click here to display 35 evidence detail records.
HumanTBX16899T-box 1
Click here to display 35 evidence detail records.
HumanSMO6608smoothened, frizzled family receptor
INFERRED
HumanSIX16495SIX homeobox 1
Click here to display 35 evidence detail records.
HumanRARA5914retinoic acid receptor, alpha
Click here to display 35 evidence detail records.
HumanPOU3F35455POU class 3 homeobox 3
Click here to display 35 evidence detail records.
HumanPRRX15396paired related homeobox 1
Click here to display 35 evidence detail records.
HumanOTX25015orthodenticle homeobox 2
Click here to display 35 evidence detail records.
HumanTNFRSF11B4982tumor necrosis factor receptor superfamily, member 11b
Click here to display 35 evidence detail records.
HumanHOXA23199homeobox A2
Click here to display 35 evidence detail records.
HumanHOXA13198homeobox A1
Click here to display 35 evidence detail records.
HumanGNA112767guanine nucleotide binding protein (G protein), alpha 11 (Gq class)
Click here to display 35 evidence detail records.
HumanFOXC22303forkhead box C2 (MFH-1, mesenchyme forkhead 1)
INFERRED
HumanFGFR32261fibroblast growth factor receptor 3
Click here to display 35 evidence detail records.
HumanFGFR12260fibroblast growth factor receptor 1
Click here to display 35 evidence detail records.
HumanEYA12138eyes absent homolog 1 (Drosophila)
Click here to display 35 evidence detail records.
HumanEMX22018empty spiracles homeobox 2
Click here to display 35 evidence detail records.
HumanEDNRA1909endothelin receptor type A
Click here to display 35 evidence detail records.
HumanECE11889endothelin converting enzyme 1
INFERRED
HumanDLX21746distal-less homeobox 2
Click here to display 35 evidence detail records.
HumanDLX11745distal-less homeobox 1
Click here to display 35 evidence detail records.
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0005106abnormal incus morphology0self