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Details
Link-It Detail - Jax Mouse Phenotype - abnormal stapes morphology
Debug Stats
  • ### Total Build Time: 263 ms 24.715 KB
  • CONCEPT_NAME gt=9 ms Completed: 9 ms rowSize= 380 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 237 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 173 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=7 ms Completed: 7 ms rowSize= 593 bytes
  • CONCEPT_CHILDREN gt=6 ms Completed: 6 ms rowSize= 1.481 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 4.284 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=240 ms Completed: 240 ms rowSize= 16.290 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.164 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal stapes morphology MP:0005107
Definition (1)
any structural anomaly of the smallest and innermost of the three auditory ossicles
Synonyms (1)
"abnormal stapes" EXACT
Parents (1)
img abnormal middle ear ossicle morphology MP:0005105
Children (3)
img abnormal stapedial artery morphology MP:0004665
img absent stapes MP:0004204
img abnormal stapes footplate morphology MP:0004290
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 (28)

Species:
human : 28
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanGDF6392255growth differentiation factor 6
Click here to display 40 evidence detail records.
HumanCHD755636chromodomain helicase DNA binding protein 7
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HumanNOG9241noggin
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HumanPAX87849paired box 8
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HumanWNT17471wingless-type MMTV integration site family, member 1
INFERRED
HumanTFAP2A7020transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
Click here to display 40 evidence detail records.
HumanTBX16899T-box 1
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HumanSMO6608smoothened, frizzled family receptor
INFERRED
HumanSIX16495SIX homeobox 1
Click here to display 40 evidence detail records.
HumanRARA5914retinoic acid receptor, alpha
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HumanPOU3F35455POU class 3 homeobox 3
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HumanPRRX15396paired related homeobox 1
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HumanPBX15087pre-B-cell leukemia homeobox 1
INFERRED
HumanTNFRSF11B4982tumor necrosis factor receptor superfamily, member 11b
Click here to display 40 evidence detail records.
HumanNAGLU4669N-acetylglucosaminidase, alpha
Click here to display 40 evidence detail records.
HumanHOXA23199homeobox A2
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HumanHOXA13198homeobox A1
INFERRED
HumanGNA112767guanine nucleotide binding protein (G protein), alpha 11 (Gq class)
Click here to display 40 evidence detail records.
HumanFOXC22303forkhead box C2 (MFH-1, mesenchyme forkhead 1)
INFERRED
HumanFGFR32261fibroblast growth factor receptor 3
Click here to display 40 evidence detail records.
HumanFGFR12260fibroblast growth factor receptor 1
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HumanEYA12138eyes absent homolog 1 (Drosophila)
Click here to display 40 evidence detail records.
HumanEMX22018empty spiracles homeobox 2
Click here to display 40 evidence detail records.
HumanEDNRA1909endothelin receptor type A
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HumanECE11889endothelin converting enzyme 1
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0005107abnormal stapes morphology0self