| Category | Name | IntersectionWithQuery | PValue | GenesInTerm | GenesInQuery | GenesInTermInQuery | ID |
|---|---|---|---|---|---|---|---|
| GeneOntologyBiologicalProcess | sensory perception of mechanical stimulus | 2.21e-05 | 238 | 30 | 5 | GO:0050954 | |
| GeneOntologyBiologicalProcess | inner ear morphogenesis | 3.53e-05 | 129 | 30 | 4 | GO:0042472 | |
| GeneOntologyBiologicalProcess | actin filament-based movement | 6.86e-05 | 153 | 30 | 4 | GO:0030048 | |
| GeneOntologyBiologicalProcess | ear morphogenesis | 7.04e-05 | 154 | 30 | 4 | GO:0042471 | |
| GeneOntologyBiologicalProcess | equilibrioception | 7.32e-05 | 9 | 30 | 2 | GO:0050957 | |
| GeneOntologyBiologicalProcess | sensory perception of sound | 1.86e-04 | 198 | 30 | 4 | GO:0007605 | |
| GeneOntologyBiologicalProcess | cardiac muscle cell contraction | 3.30e-04 | 93 | 30 | 3 | GO:0086003 | |
| GeneOntologyCellularComponent | nuclear speck | 2.90e-05 | 431 | 30 | 6 | GO:0016607 | |
| GeneOntologyCellularComponent | voltage-gated sodium channel complex | 2.67e-04 | 17 | 30 | 2 | GO:0001518 | |
| GeneOntologyCellularComponent | sodium channel complex | 7.89e-04 | 29 | 30 | 2 | GO:0034706 | |
| GeneOntologyCellularComponent | nuclear body | 1.56e-03 | 903 | 30 | 6 | GO:0016604 | |
| GeneOntologyCellularComponent | monoatomic ion channel complex | 1.99e-03 | 378 | 30 | 4 | GO:0034702 | |
| GeneOntologyCellularComponent | photoreceptor connecting cilium | 2.16e-03 | 48 | 30 | 2 | GO:0032391 | |
| GeneOntologyCellularComponent | ciliary base | 2.92e-03 | 56 | 30 | 2 | GO:0097546 | |
| GeneOntologyCellularComponent | myosin complex | 3.24e-03 | 59 | 30 | 2 | GO:0016459 | |
| GeneOntologyCellularComponent | cluster of actin-based cell projections | 3.93e-03 | 223 | 30 | 3 | GO:0098862 | |
| GeneOntologyCellularComponent | stereocilium | 4.40e-03 | 69 | 30 | 2 | GO:0032420 | |
| GeneOntologyCellularComponent | membrane protein complex | 4.51e-03 | 1498 | 30 | 7 | GO:0098796 | |
| GeneOntologyCellularComponent | cation channel complex | 4.55e-03 | 235 | 30 | 3 | GO:0034703 | |
| GeneOntologyCellularComponent | photoreceptor inner segment | 5.59e-03 | 78 | 30 | 2 | GO:0001917 | |
| GeneOntologyCellularComponent | stereocilium bundle | 5.73e-03 | 79 | 30 | 2 | GO:0032421 | |
| GeneOntologyCellularComponent | ciliary transition zone | 6.01e-03 | 81 | 30 | 2 | GO:0035869 | |
| GeneOntologyCellularComponent | transmembrane transporter complex | 6.34e-03 | 523 | 30 | 4 | GO:1902495 | |
| GeneOntologyCellularComponent | actin-based cell projection | 7.24e-03 | 278 | 30 | 3 | GO:0098858 | |
| GeneOntologyCellularComponent | lateral plasma membrane | 7.37e-03 | 90 | 30 | 2 | GO:0016328 | |
| GeneOntologyCellularComponent | transporter complex | 7.55e-03 | 550 | 30 | 4 | GO:1990351 | |
| MousePheno | abnormal cochlear hair cell inter-stereocilial links morphology | 4.76e-07 | 9 | 26 | 3 | MP:0004577 | |
| MousePheno | absent cochlear hair cells | 1.24e-06 | 12 | 26 | 3 | MP:0004405 | |
| MousePheno | abnormal inner hair cell stereociliary bundle morphology | 1.33e-06 | 45 | 26 | 4 | MP:0004532 | |
| MousePheno | vestibular saccular macula degeneration | 1.61e-06 | 13 | 26 | 3 | MP:0004331 | |
| MousePheno | decreased cochlear hair cell number | 2.59e-06 | 53 | 26 | 4 | MP:0004408 | |
| MousePheno | abnormal otolith organ morphology | 3.01e-06 | 55 | 26 | 4 | MP:0004425 | |
| MousePheno | abnormal utricular macula morphology | 3.82e-06 | 17 | 26 | 3 | MP:0004333 | |
| MousePheno | abnormal vestibular saccular macula morphology | 6.38e-06 | 20 | 26 | 3 | MP:0004330 | |
| MousePheno | abnormal stationary movement | 6.61e-06 | 147 | 26 | 5 | MP:0001388 | |
| MousePheno | abnormal cochlear hair cell number | 7.06e-06 | 68 | 26 | 4 | MP:0004406 | |
| MousePheno | head shaking | 8.59e-06 | 22 | 26 | 3 | MP:0002730 | |
| MousePheno | abnormal vestibular labyrinth morphology | 1.35e-05 | 80 | 26 | 4 | MP:0004427 | |
| MousePheno | impaired swimming | 1.35e-05 | 80 | 26 | 4 | MP:0001522 | |
| MousePheno | abnormal inner ear vestibule morphology | 1.42e-05 | 81 | 26 | 4 | MP:0000034 | |
| MousePheno | abnormal cochlear hair cell stereociliary bundle morphology | 2.25e-05 | 91 | 26 | 4 | MP:0004521 | |
| MousePheno | abnormal pinna reflex | 3.40e-05 | 101 | 26 | 4 | MP:0001485 | |
| MousePheno | head tossing | 3.59e-05 | 35 | 26 | 3 | MP:0005307 | |
| MousePheno | abnormal head movements | 3.67e-05 | 103 | 26 | 4 | MP:0000436 | |
| MousePheno | cochlear hair cell degeneration | 4.11e-05 | 106 | 26 | 4 | MP:0004362 | |
| MousePheno | abnormal sensory ganglion morphology | 4.74e-05 | 221 | 26 | 5 | MP:0000960 | |
| MousePheno | short cochlear outer hair cells | 4.97e-05 | 6 | 26 | 2 | MP:0004466 | |
| MousePheno | abnormal cochlear hair cell physiology | 5.39e-05 | 40 | 26 | 3 | MP:0004432 | |
| MousePheno | abnormal utricle morphology | 5.81e-05 | 41 | 26 | 3 | MP:0006090 | |
| MousePheno | absent distortion product otoacoustic emissions | 5.81e-05 | 41 | 26 | 3 | MP:0004737 | |
| MousePheno | deafness | 5.84e-05 | 116 | 26 | 4 | MP:0001967 | |
| MousePheno | circling | 6.04e-05 | 117 | 26 | 4 | MP:0001394 | |
| MousePheno | head tilt | 7.19e-05 | 44 | 26 | 3 | MP:0005191 | |
| MousePheno | abnormal stria vascularis morphology | 7.19e-05 | 44 | 26 | 3 | MP:0000048 | |
| MousePheno | abnormal cochlear inner hair cell morphology | 7.58e-05 | 124 | 26 | 4 | MP:0004393 | |
| MousePheno | abnormal vestibular saccule morphology | 8.22e-05 | 46 | 26 | 3 | MP:0006089 | |
| MousePheno | abnormal vestibular hair cell morphology | 9.35e-05 | 48 | 26 | 3 | MP:0002623 | |
| MousePheno | abnormal hair cell physiology | 9.94e-05 | 49 | 26 | 3 | MP:0003879 | |
| MousePheno | abnormal vestibular system physiology | 9.94e-05 | 49 | 26 | 3 | MP:0004742 | |
| MousePheno | head bobbing | 1.12e-04 | 51 | 26 | 3 | MP:0001410 | |
| MousePheno | thin stria vascularis | 1.48e-04 | 10 | 26 | 2 | MP:0004364 | |
| MousePheno | absent cochlear microphonics | 1.48e-04 | 10 | 26 | 2 | MP:0004413 | |
| MousePheno | neurodegeneration | 1.77e-04 | 468 | 26 | 6 | MP:0002229 | |
| MousePheno | abnormal cochlear outer hair cell morphology | 1.98e-04 | 159 | 26 | 4 | MP:0004399 | |
| MousePheno | cochlear degeneration | 2.01e-04 | 62 | 26 | 3 | MP:0000032 | |
| MousePheno | fused inner hair cell stereocilia | 2.17e-04 | 12 | 26 | 2 | MP:0004533 | |
| MousePheno | abnormal outer hair cell stereociliary bundle morphology | 2.64e-04 | 68 | 26 | 3 | MP:0004527 | |
| MousePheno | abnormal cranial ganglia morphology | 2.86e-04 | 175 | 26 | 4 | MP:0001081 | |
| MousePheno | stria vascularis degeneration | 2.99e-04 | 14 | 26 | 2 | MP:0004363 | |
| MousePheno | increased type II pneumocyte number | 2.99e-04 | 14 | 26 | 2 | MP:0010810 | |
| MousePheno | abnormal sensory neuron physiology | 3.13e-04 | 72 | 26 | 3 | MP:0010055 | |
| MousePheno | decreased sensory neuron number | 3.25e-04 | 181 | 26 | 4 | MP:0000966 | |
| MousePheno | vestibular hair cell degeneration | 3.44e-04 | 15 | 26 | 2 | MP:0004324 | |
| MousePheno | short cochlear hair cell stereocilia | 4.45e-04 | 17 | 26 | 2 | MP:0004524 | |
| MousePheno | abnormal somatic nervous system physiology | 4.76e-04 | 83 | 26 | 3 | MP:0005423 | |
| MousePheno | abnormal cochlear hair cell morphology | 4.93e-04 | 202 | 26 | 4 | MP:0002622 | |
| MousePheno | abnormal cochlear microphonics | 5.00e-04 | 18 | 26 | 2 | MP:0004412 | |
| MousePheno | abnormal distortion product otoacoustic emission | 5.10e-04 | 85 | 26 | 3 | MP:0004736 | |
| MousePheno | abnormal otoacoustic response | 5.28e-04 | 86 | 26 | 3 | MP:0006336 | |
| MousePheno | cochlear outer hair cell degeneration | 5.28e-04 | 86 | 26 | 3 | MP:0004404 | |
| MousePheno | abnormal cochlear sensory epithelium morphology | 5.41e-04 | 207 | 26 | 4 | MP:0003308 | |
| MousePheno | abnormal cochlear potential | 5.58e-04 | 19 | 26 | 2 | MP:0006332 | |
| MousePheno | abnormal organ of Corti morphology | 5.61e-04 | 209 | 26 | 4 | MP:0000042 | |
| MousePheno | abnormal cochlear ganglion morphology | 5.64e-04 | 88 | 26 | 3 | MP:0002855 | |
| MousePheno | decreased neuron number | 5.66e-04 | 376 | 26 | 5 | MP:0008948 | |
| MousePheno | absent pinna reflex | 5.83e-04 | 89 | 26 | 3 | MP:0006358 | |
| MousePheno | stereotypic behavior | 6.13e-04 | 214 | 26 | 4 | MP:0001408 | |
| MousePheno | abnormal hair cell morphology | 6.13e-04 | 214 | 26 | 4 | MP:0000045 | |
| MousePheno | absent linear vestibular evoked potential | 6.19e-04 | 20 | 26 | 2 | MP:0004813 | |
| MousePheno | neuron degeneration | 6.76e-04 | 391 | 26 | 5 | MP:0003224 | |
| MousePheno | impaired hearing | 7.15e-04 | 223 | 26 | 4 | MP:0006325 | |
| MousePheno | abnormal vestibular hair cell stereociliary bundle morphology | 7.51e-04 | 22 | 26 | 2 | MP:0004515 | |
| MousePheno | abnormal dorsal-ventral axis patterning | 7.51e-04 | 22 | 26 | 2 | MP:0001704 | |
| MousePheno | abnormal mechanoreceptor morphology | 8.16e-04 | 231 | 26 | 4 | MP:0000972 | |
| MousePheno | abnormal cochlear labyrinth morphology | 8.70e-04 | 235 | 26 | 4 | MP:0004426 | |
| MousePheno | abnormal scala media morphology | 8.70e-04 | 235 | 26 | 4 | MP:0003169 | |
| MousePheno | increased or absent threshold for auditory brainstem response | 8.84e-04 | 236 | 26 | 4 | MP:0011967 | |
| MousePheno | bidirectional circling | 8.95e-04 | 24 | 26 | 2 | MP:0001395 | |
| MousePheno | small dorsal root ganglion | 8.95e-04 | 24 | 26 | 2 | MP:0000964 | |
| MousePheno | decreased incisor number | 8.95e-04 | 24 | 26 | 2 | MP:0030609 | |
| MousePheno | abnormal cochlea morphology | 1.06e-03 | 248 | 26 | 4 | MP:0000031 | |
| MousePheno | abnormal cochlear outer hair cell physiology | 1.22e-03 | 28 | 26 | 2 | MP:0004434 | |
| MousePheno | abnormal membranous labyrinth morphology | 1.30e-03 | 262 | 26 | 4 | MP:0000035 | |
| MousePheno | abnormal tail movements | 1.31e-03 | 29 | 26 | 2 | MP:0001391 | |
| MousePheno | abnormal neuron number | 1.35e-03 | 456 | 26 | 5 | MP:0008946 | |
| MousePheno | abnormal linear vestibular evoked potential | 1.40e-03 | 30 | 26 | 2 | MP:0004812 | |
| MousePheno | abnormal basicranium morphology | 1.49e-03 | 123 | 26 | 3 | MP:0010029 | |
| MousePheno | abnormal somatic sensory system morphology | 1.52e-03 | 702 | 26 | 6 | MP:0000959 | |
| MousePheno | abnormal ear morphology | 1.54e-03 | 470 | 26 | 5 | MP:0002102 | |
| MousePheno | abnormal tectorial membrane morphology | 1.59e-03 | 32 | 26 | 2 | MP:0003149 | |
| MousePheno | increased neural tube apoptosis | 1.70e-03 | 33 | 26 | 2 | MP:0012505 | |
| MousePheno | abnormal reflex | 1.80e-03 | 1294 | 26 | 8 | MP:0001961 | |
| MousePheno | abnormal locomotor coordination | 1.81e-03 | 726 | 26 | 6 | MP:0003312 | |
| MousePheno | abnormal orientation of cochlear hair cell stereociliary bundles | 1.91e-03 | 35 | 26 | 2 | MP:0004522 | |
| Domain | IQ_motif_EF-hand-BS | 1.09e-05 | 90 | 29 | 4 | IPR000048 | |
| Domain | MYTH4 | 8.32e-05 | 9 | 29 | 2 | PS51016 | |
| Domain | MyTH4_dom | 8.32e-05 | 9 | 29 | 2 | IPR000857 | |
| Domain | MyTH4 | 8.32e-05 | 9 | 29 | 2 | SM00139 | |
| Domain | MyTH4 | 8.32e-05 | 9 | 29 | 2 | PF00784 | |
| Domain | Na_channel_asu | 1.04e-04 | 10 | 29 | 2 | IPR001696 | |
| Domain | Na_trans_assoc | 1.04e-04 | 10 | 29 | 2 | IPR010526 | |
| Domain | Na_trans_assoc | 1.04e-04 | 10 | 29 | 2 | PF06512 | |
| Domain | IQ | 1.79e-04 | 71 | 29 | 3 | PF00612 | |
| Domain | IQ | 2.65e-04 | 81 | 29 | 3 | SM00015 | |
| Domain | IQ | 3.98e-04 | 93 | 29 | 3 | PS50096 | |
| Domain | MYOSIN_MOTOR | 1.58e-03 | 38 | 29 | 2 | PS51456 | |
| Domain | Myosin_head | 1.58e-03 | 38 | 29 | 2 | PF00063 | |
| Domain | Myosin_head_motor_dom | 1.58e-03 | 38 | 29 | 2 | IPR001609 | |
| Domain | MYSc | 1.58e-03 | 38 | 29 | 2 | SM00242 | |
| Domain | FERM_M | 2.31e-03 | 46 | 29 | 2 | PF00373 | |
| Domain | FERM_central | 2.62e-03 | 49 | 29 | 2 | IPR019748 | |
| Domain | FERM_domain | 2.62e-03 | 49 | 29 | 2 | IPR000299 | |
| Domain | FERM_1 | 2.72e-03 | 50 | 29 | 2 | PS00660 | |
| Domain | FERM_2 | 2.72e-03 | 50 | 29 | 2 | PS00661 | |
| Domain | Band_41_domain | 2.72e-03 | 50 | 29 | 2 | IPR019749 | |
| Domain | B41 | 2.72e-03 | 50 | 29 | 2 | SM00295 | |
| Domain | FERM_3 | 2.72e-03 | 50 | 29 | 2 | PS50057 | |
| Domain | Channel_four-helix_dom | 3.52e-03 | 57 | 29 | 2 | IPR027359 | |
| Domain | - | 3.52e-03 | 57 | 29 | 2 | 1.20.120.350 | |
| Domain | SH3 | 4.47e-03 | 216 | 29 | 3 | PS50002 | |
| Domain | SH3 | 4.47e-03 | 216 | 29 | 3 | SM00326 | |
| Domain | SH3_domain | 4.70e-03 | 220 | 29 | 3 | IPR001452 | |
| Domain | SH3_2 | 7.85e-03 | 86 | 29 | 2 | IPR011511 | |
| Domain | SH3_2 | 7.85e-03 | 86 | 29 | 2 | PF07653 | |
| Domain | TPR_1 | 8.57e-03 | 90 | 29 | 2 | PF00515 | |
| Domain | TPR_1 | 8.57e-03 | 90 | 29 | 2 | IPR001440 | |
| Domain | Ion_trans_dom | 1.35e-02 | 114 | 29 | 2 | IPR005821 | |
| Domain | Ion_trans | 1.35e-02 | 114 | 29 | 2 | PF00520 | |
| Pathway | REACTOME_SENSORY_PROCESSING_OF_SOUND_BY_OUTER_HAIR_CELLS_OF_THE_COCHLEA | 1.37e-04 | 55 | 26 | 3 | M41823 | |
| Pathway | REACTOME_SENSORY_PROCESSING_OF_SOUND | 3.72e-04 | 77 | 26 | 3 | M41822 | |
| Pubmed | Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review. | 2.32e-09 | 4 | 30 | 3 | 27743438 | |
| Pubmed | 2.02e-08 | 7 | 30 | 3 | 21436032 | ||
| Pubmed | Investigation of MYO15A and MYO7A Mutations in Iranian Patients with Nonsyndromic Hearing Loss. | 7.19e-07 | 2 | 30 | 2 | 31997689 | |
| Pubmed | Structure of MyTH4-FERM domains in myosin VIIa tail bound to cargo. | 7.19e-07 | 2 | 30 | 2 | 21311020 | |
| Pubmed | Cy3-ATP labeling of unfixed, permeabilized mouse hair cells. | 7.19e-07 | 2 | 30 | 2 | 34903829 | |
| Pubmed | Novel mutations of MYO7A and USH1G in Israeli Arab families with Usher syndrome type 1. | 2.16e-06 | 3 | 30 | 2 | 22219650 | |
| Pubmed | Genetic analysis through OtoSeq of Pakistani families segregating prelingual hearing loss. | 2.16e-06 | 3 | 30 | 2 | 23770805 | |
| Pubmed | 2.16e-06 | 3 | 30 | 2 | 15654330 | ||
| Pubmed | 2.16e-06 | 3 | 30 | 2 | 28660889 | ||
| Pubmed | 4.31e-06 | 4 | 30 | 2 | 31644917 | ||
| Pubmed | 4.31e-06 | 4 | 30 | 2 | 15590698 | ||
| Pubmed | 4.31e-06 | 4 | 30 | 2 | 30275467 | ||
| Pubmed | 4.31e-06 | 4 | 30 | 2 | 10198179 | ||
| Pubmed | 4.31e-06 | 4 | 30 | 2 | 12966030 | ||
| Pubmed | The role of mouse mutants in the identification of human hereditary hearing loss genes. | 4.31e-06 | 4 | 30 | 2 | 10320095 | |
| Pubmed | Analysis of subcellular localization of Myo7a, Pcdh15 and Sans in Ush1c knockout mice. | 4.31e-06 | 4 | 30 | 2 | 21156003 | |
| Pubmed | 7.18e-06 | 5 | 30 | 2 | 22381527 | ||
| Pubmed | 7.18e-06 | 5 | 30 | 2 | 12588794 | ||
| Pubmed | Interactions in the network of Usher syndrome type 1 proteins. | 7.18e-06 | 5 | 30 | 2 | 15590703 | |
| Pubmed | 7.18e-06 | 5 | 30 | 2 | 20332152 | ||
| Pubmed | Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population. | 7.18e-06 | 5 | 30 | 2 | 15660226 | |
| Pubmed | 7.18e-06 | 5 | 30 | 2 | 16219682 | ||
| Pubmed | Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F. | 7.18e-06 | 5 | 30 | 2 | 11398101 | |
| Pubmed | Dispersed DNA variants underlie hearing loss in South Florida's minority population. | 7.18e-06 | 5 | 30 | 2 | 37996878 | |
| Pubmed | 7.18e-06 | 5 | 30 | 2 | 18160714 | ||
| Pubmed | ZBTB20 is essential for cochlear maturation and hearing in mice. | 9.15e-06 | 47 | 30 | 3 | 37279265 | |
| Pubmed | 1.08e-05 | 6 | 30 | 2 | 26620972 | ||
| Pubmed | 1.08e-05 | 6 | 30 | 2 | 9927480 | ||
| Pubmed | LncRNAs-directed PTEN enzymatic switch governs epithelial-mesenchymal transition. | 1.31e-05 | 168 | 30 | 4 | 30631154 | |
| Pubmed | 1.51e-05 | 7 | 30 | 2 | 10722873 | ||
| Pubmed | 1.51e-05 | 7 | 30 | 2 | 11212352 | ||
| Pubmed | 1.51e-05 | 7 | 30 | 2 | 28031293 | ||
| Pubmed | 1.51e-05 | 7 | 30 | 2 | 13853422 | ||
| Pubmed | 1.51e-05 | 7 | 30 | 2 | 20301442 | ||
| Pubmed | 2.01e-05 | 8 | 30 | 2 | 16545802 | ||
| Pubmed | Microarray-based mutation analysis of 183 Spanish families with Usher syndrome. | 2.01e-05 | 8 | 30 | 2 | 19683999 | |
| Pubmed | Stereocilin connects outer hair cell stereocilia to one another and to the tectorial membrane. | 2.01e-05 | 8 | 30 | 2 | 21165971 | |
| Pubmed | 2.01e-05 | 8 | 30 | 2 | 18484607 | ||
| Pubmed | 2.01e-05 | 8 | 30 | 2 | 15702992 | ||
| Pubmed | 2.58e-05 | 9 | 30 | 2 | 19339464 | ||
| Pubmed | 2.58e-05 | 9 | 30 | 2 | 18339676 | ||
| Pubmed | 3.05e-05 | 70 | 30 | 3 | 20301607 | ||
| Pubmed | Massively parallel DNA sequencing facilitates diagnosis of patients with Usher syndrome type 1. | 3.22e-05 | 10 | 30 | 2 | 24618850 | |
| Pubmed | 3.22e-05 | 10 | 30 | 2 | 24239741 | ||
| Pubmed | 3.94e-05 | 11 | 30 | 2 | 36252002 | ||
| Pubmed | 3.94e-05 | 11 | 30 | 2 | 12642503 | ||
| Pubmed | 3.94e-05 | 11 | 30 | 2 | 31776257 | ||
| Pubmed | Molecular mechanisms underlying inner ear patterning defects in kreisler mutants. | 4.72e-05 | 12 | 30 | 2 | 16325169 | |
| Pubmed | Reciprocal Negative Regulation Between Lmx1a and Lmo4 Is Required for Inner Ear Formation. | 4.72e-05 | 12 | 30 | 2 | 29769265 | |
| Pubmed | CIB2 interacts with TMC1 and TMC2 and is essential for mechanotransduction in auditory hair cells. | 4.72e-05 | 12 | 30 | 2 | 28663585 | |
| Pubmed | Class III myosins shape the auditory hair bundles by limiting microvilli and stereocilia growth. | 6.50e-05 | 14 | 30 | 2 | 26754646 | |
| Pubmed | Disorganized innervation and neuronal loss in the inner ear of Slitrk6-deficient mice. | 6.50e-05 | 14 | 30 | 2 | 19936227 | |
| Pubmed | Functional equivalence of Brn3 POU-domain transcription factors in mouse retinal neurogenesis. | 8.57e-05 | 16 | 30 | 2 | 15647317 | |
| Pubmed | 9.70e-05 | 17 | 30 | 2 | 15242798 | ||
| Pubmed | CTDP1 regulates breast cancer survival and DNA repair through BRCT-specific interactions with FANCI. | 9.94e-05 | 104 | 30 | 3 | 31240132 | |
| Pubmed | Identification of genes concordantly expressed with Atoh1 during inner ear development. | 1.22e-04 | 19 | 30 | 2 | 21519551 | |
| Pubmed | A quantitative survey of gravity receptor function in mutant mouse strains. | 1.35e-04 | 20 | 30 | 2 | 16235133 | |
| Pubmed | 1.63e-04 | 322 | 30 | 4 | 26514267 | ||
| Pubmed | 1.64e-04 | 22 | 30 | 2 | 19223390 | ||
| Pubmed | A systematic survey of carbonic anhydrase mRNA expression during mammalian inner ear development. | 1.64e-04 | 22 | 30 | 2 | 23233153 | |
| Pubmed | The small GTPase Rac1 regulates auditory hair cell morphogenesis. | 1.80e-04 | 23 | 30 | 2 | 20016102 | |
| Pubmed | 1.80e-04 | 23 | 30 | 2 | 20932654 | ||
| Pubmed | Notch signaling is essential for ventricular chamber development. | 2.49e-04 | 27 | 30 | 2 | 17336907 | |
| Pubmed | 2.58e-04 | 363 | 30 | 4 | 25036637 | ||
| Pubmed | 2.68e-04 | 28 | 30 | 2 | 20346939 | ||
| Pubmed | Fgf10 is required for specification of non-sensory regions of the cochlear epithelium. | 2.88e-04 | 29 | 30 | 2 | 25624266 | |
| Pubmed | 3.51e-04 | 32 | 30 | 2 | 23704327 | ||
| Pubmed | 3.74e-04 | 33 | 30 | 2 | 24727668 | ||
| Pubmed | 3.97e-04 | 34 | 30 | 2 | 18590716 | ||
| Pubmed | Novel gene function revealed by mouse mutagenesis screens for models of age-related disease. | 6.65e-04 | 44 | 30 | 2 | 27534441 | |
| Pubmed | 7.92e-04 | 48 | 30 | 2 | 8884266 | ||
| Pubmed | 8.25e-04 | 49 | 30 | 2 | 10051400 | ||
| Pubmed | Regulation of the CUL3 Ubiquitin Ligase by a Calcium-Dependent Co-adaptor. | 8.59e-04 | 50 | 30 | 2 | 27716508 | |
| Cytoband | 9p13.3 | 1.11e-03 | 75 | 30 | 2 | 9p13.3 | |
| GeneFamily | Actins|Deafness associated genes | 3.36e-04 | 113 | 22 | 3 | 1152 | |
| GeneFamily | Ankyrin repeat domain containing|FERM domain containing | 1.67e-03 | 50 | 22 | 2 | 1293 | |
| GeneFamily | Tetratricopeptide repeat domain containing|Bardet-Biedl syndrome associated|BBSome | 8.53e-03 | 115 | 22 | 2 | 769 | |
| GeneFamily | RNA binding motif containing | 2.73e-02 | 213 | 22 | 2 | 725 | |
| Coexpression | GSE7768_OVA_ALONE_VS_OVA_WITH_MPL_IMMUNIZED_MOUSE_WHOLE_SPLEEN_6H_UP | 5.24e-05 | 181 | 30 | 4 | M6857 | |
| Coexpression | GSE1566_WT_VS_EZH2_KO_LN_TCELL_DN | 7.42e-05 | 198 | 30 | 4 | M6224 | |
| Coexpression | GSE2770_IL12_VS_TGFB_AND_IL12_TREATED_ACT_CD4_TCELL_6H_DN | 7.57e-05 | 199 | 30 | 4 | M6060 | |
| ToppCell | facs-Brain_Non-Myeloid-Striatum-24m-Mesenchymal|Brain_Non-Myeloid / Brain_Non-Myeloid_Brain_Myeloid - method, tissue, subtissue, age, lineage, cell ontology and free annotation | 5.86e-06 | 177 | 30 | 4 | e8bb4f8ecd5e283efec966b9fc2040a6152d5551 | |
| ToppCell | facs-Brain_Non-Myeloid-Striatum-24m-Mesenchymal-Ependyma|Brain_Non-Myeloid / Brain_Non-Myeloid_Brain_Myeloid - method, tissue, subtissue, age, lineage, cell ontology and free annotation | 5.99e-06 | 178 | 30 | 4 | 579cdc14f28b459e200ae2102e0bd4df8a2c0dcb | |
| ToppCell | facs-Brain_Non-Myeloid-Striatum-24m-Mesenchymal-ependymal_cell|Brain_Non-Myeloid / Brain_Non-Myeloid_Brain_Myeloid - method, tissue, subtissue, age, lineage, cell ontology and free annotation | 5.99e-06 | 178 | 30 | 4 | b1db59344c074c7c80169fc2c5cd5fc89f3fe463 | |
| Drug | Hippeastrine hydrobromide [22352-41-6]; Up 200; 10uM; PC3; HT_HG-U133A | 5.65e-06 | 198 | 30 | 5 | 7381_UP | |
| Disease | hearing impairment | 2.93e-06 | 98 | 30 | 4 | C1384666 | |
| Disease | Usher syndrome, type 1A | 9.97e-06 | 5 | 30 | 2 | C2931205 | |
| Disease | USHER SYNDROME, TYPE IB (disorder) | 9.97e-06 | 5 | 30 | 2 | C1848638 | |
| Disease | USHER SYNDROME, TYPE IA, FORMERLY | 9.97e-06 | 5 | 30 | 2 | C1848639 | |
| Disease | USHER SYNDROME, TYPE I, FRENCH VARIETY, FORMERLY | 9.97e-06 | 5 | 30 | 2 | C1848640 | |
| Disease | Usher syndrome type 1 | 9.97e-06 | 5 | 30 | 2 | cv:C1568247 | |
| Disease | Hereditary hearing loss and deafness | 1.43e-05 | 146 | 30 | 4 | cv:C0236038 | |
| Disease | Usher Syndrome, Type I | 1.50e-05 | 6 | 30 | 2 | C1568247 | |
| Disease | Nonsyndromic Hearing Loss and Deafness, Autosomal Recessive | 1.91e-05 | 51 | 30 | 3 | cv:CN043650 | |
| Disease | Hereditary retinal dystrophy | 2.09e-05 | 7 | 30 | 2 | C0154860 | |
| Disease | Usher syndrome | 2.09e-05 | 7 | 30 | 2 | cv:C0271097 | |
| Disease | generalized epilepsy with febrile seizures plus 2 (implicated_via_orthology) | 4.47e-05 | 10 | 30 | 2 | DOID:0111294 (implicated_via_orthology) | |
| Disease | Dravet syndrome (implicated_via_orthology) | 4.47e-05 | 10 | 30 | 2 | DOID:0080422 (implicated_via_orthology) | |
| Disease | Nonsyndromic genetic hearing loss | 6.34e-05 | 76 | 30 | 3 | cv:C5680182 | |
| Disease | generalized epilepsy with febrile seizures plus (implicated_via_orthology) | 6.55e-05 | 12 | 30 | 2 | DOID:0060170 (implicated_via_orthology) | |
| Disease | Nonsyndromic Deafness | 7.67e-05 | 81 | 30 | 3 | C3711374 | |
| Disease | sensorineural hearing loss (is_implicated_in) | 5.17e-04 | 33 | 30 | 2 | DOID:10003 (is_implicated_in) | |
| Disease | heart function measurement | 5.49e-04 | 34 | 30 | 2 | EFO_0004311 | |
| Disease | response to radiation, prostate carcinoma, erectile dysfunction | 6.51e-04 | 37 | 30 | 2 | EFO_0001663, EFO_0004234, GO_0009314 | |
| Disease | QRS complex, QRS duration | 9.63e-04 | 45 | 30 | 2 | EFO_0005054, EFO_0005055 |
| Peptide | Gene | Start | Entry |
|---|---|---|---|
| ELPWDELDLGLDEDL | 371 | Q495M9 | |
| EPELDLDLDLEAEED | 1006 | P21860 | |
| PDLDPDVELEDAEEE | 11 | Q9Y4B4 | |
| EDDPLGEEDLPSEED | 56 | Q16790 | |
| ELSDLDDFDPLEAEP | 256 | P78413 | |
| PELDEDDLEAELDAL | 156 | Q9NZZ3 | |
| PLDENDLEEDVDSEP | 1066 | Q7RTP6 | |
| LDIPLPLGDADEEED | 501 | Q9UKN7 | |
| PLGDADEEEDEEELP | 506 | Q9UKN7 | |
| EEELPEADDLDGLLS | 621 | Q8N3J3 | |
| EADDLDGLLSELPED | 626 | Q8N3J3 | |
| ADLGLPEDDLVLPDD | 1051 | P10070 | |
| DLPDLDPECRELLLD | 76 | Q86WC4 | |
| DPERLEPGLDEEDTD | 466 | P51956 | |
| EDEEDLDPDLDPDLE | 41 | C9JE40 | |
| LDPDLDPDLEEEEND | 46 | C9JE40 | |
| ESEELEPEELLLEPE | 51 | Q86U42 | |
| EEEEEEDDLSELPPL | 41 | Q14318 | |
| LLAELDDDEDLPEPD | 1671 | Q9ULT8 | |
| DVEEDLELPPELDIS | 881 | P53621 | |
| IPDDDDLPTAEELED | 346 | O14958 | |
| PAAQPDDEEDEEELL | 576 | Q6NYC8 | |
| DALLLEDERDELEDP | 16 | Q9C0B2 | |
| LSLLDDDEEDEELPR | 366 | Q5H9M0 | |
| LPEPDDLDDPELLMD | 441 | Q8TF17 | |
| PLPDSDEDEELDLGL | 576 | Q9UPS6 | |
| EPDEDIEDLEELDIP | 616 | O43511 | |
| IPELADDLEEPDDCF | 1101 | Q9Y5Y9 | |
| LDESDDEPEKELAPE | 276 | A6NKU9 | |
| RILEPDDFLDDLDDE | 156 | Q92785 | |
| EDHEEEDLKPTPDLE | 31 | Q01118 | |
| PLILTEDDDEDDDVP | 341 | Q9BTW9 | |
| DLDAALPLPDEDEED | 981 | Q13402 |