MP:0000042 | abnormal organ of Corti | "abnormalities associated with the highly specialized epithelium in the floor of the ductus cochlearis; also referred to a spiral organ (organum spirale), or acoustic papilla" [Stedman s Medical Dictionary:ISBN 0-683-40008-8] |
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Allelic Composition: Bap1em3Test/Bap1+ Genetic Background: involves: FVB
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MP:0000218 | increased WBC count | "greater than normal WBC numbers" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Wbp2tm2a(EUCOMM)Wtsi/Wbp2tm2a(EUCOMM)Wtsi Genetic Background: C57BL/6N-Wbp2tm2a(EUCOMM)Wtsi/Cnrm
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MP:0001262 | decreased body weight | "lower than normal average weight " [J:61295] |
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Allelic Composition: Tcf7tm1a(EUCOMM)Wtsi/Tcf7tm1a(EUCOMM)Wtsi Genetic Background: C57BL/6N-Tcf7tm1a(EUCOMM)Wtsi/Ics
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MP:0001399 | hyperactivity | "general restlessness or excessive movement; more frequent movement from one place to another" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:60409, J:57125] |
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Allelic Composition: Kmt5btm1a(KOMP)Wtsi/Kmt5btm1a(KOMP)Wtsi Genetic Background: B6JTyr;B6N-Kmt5btm1a(KOMP)Wtsi/Wtsi
Allelic Composition: Wbp2tm2a(EUCOMM)Wtsi/Wbp2tm2a(EUCOMM)Wtsi Genetic Background: C57BL/6N-Wbp2tm2a(EUCOMM)Wtsi/Cnrm
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MP:0004736 | abnormal distortion product otoacoustic emission | "any abnormality in the sound produced by the cochlea in response to stimulation with 2 simultaneous tones of different frequencies; this measurement is particularly useful in assessing the functional state of OHCs" [eMedicine:http://www.emedicine.com/ent/topic372.htm, MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator", MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Bap1em3Test/Bap1+ Genetic Background: involves: FVB
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MP:0004740 | sensorineural hearing loss | "a form of progressive hearing loss due to a lesion of the auditory division of cranial nerve VIII or the inner ear" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Bap1em3Test/Bap1+ Genetic Background: involves: FVB
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MP:0004746 | abnormal cochlear IHC afferent innervation | "any changes in the morphology or number of afferent terminals and/or their synapses in the cochlear IHC region" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Bap1em3Test/Bap1+ Genetic Background: involves: FVB
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MP:0004747 | abnormal cochlear OHC afferent innervation | "any changes in the morphology or number of afferent terminals and/or their synapses in the cochlear OHC region" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"] |
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Allelic Composition: Bap1em3Test/Bap1+ Genetic Background: involves: FVB
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MP:0004924 | abnormal behavior | "anomalies in the actions, reactions, or performance of an organism in response to external or internal stimuli compared to controls" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Kmt5btm1a(KOMP)Wtsi/Kmt5btm1a(KOMP)Wtsi Genetic Background: B6JTyr;B6N-Kmt5btm1a(KOMP)Wtsi/Wtsi
Allelic Composition: Wbp2tm2a(EUCOMM)Wtsi/Wbp2tm2a(EUCOMM)Wtsi Genetic Background: C57BL/6N-Wbp2tm2a(EUCOMM)Wtsi/Cnrm
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MP:0005419 | hypoalbuminemia | "blood albumin concentration below the normal range" [MeSH:National Library of Medicine - Medical Subject Headings , 2003] |
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Allelic Composition: Kmt5btm1a(KOMP)Wtsi/Kmt5btm1a(KOMP)Wtsi Genetic Background: B6JTyr;B6N-Kmt5btm1a(KOMP)Wtsi/Wtsi
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MP:0006358 | absent pinna reflex | "complete failure to respond to an auditory stimulus by a characteristic ear twitch" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator", MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"] |
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Allelic Composition: Kmt5btm1a(KOMP)Wtsi/Kmt5btm1a(KOMP)Wtsi Genetic Background: B6JTyr;B6N-Kmt5btm1a(KOMP)Wtsi/Wtsi
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MP:0006388 | abnormal auditory summating potiential | "any anomaly in the dc shift in the waveform sustained for the duration of a toneburst stimulus that represents the depolarization of sensory hair cells in the cochlea; positive summating potentials (SPs) reflect activity of basal turn hair cells while negative SPs are derived from hair cell activity in the apical turn; negative SPs tend to be obtained at low frequencies and low intensities of stimulus, while positive SPs are recorded in response to high frequencies and high intensities " [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator", PMID:1526886] |
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Allelic Composition: Bap1em3Test/Bap1+ Genetic Background: involves: FVB
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MP:0008805 | decreased circulating amylase level | "reduction in the concentration of a group of amylolytic enzymes that cleave starch, glycogen, and related alpha-1,4-glucans in the blood" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition", MESH:D08.811.277.450.066, MGI:brs "Beverly Richards-Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Bap1em3Test/Bap1+ Genetic Background: involves: FVB
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MP:0010088 | decreased circulating fructosamine level | "decrease in the concentration in the blood of total non enzymatic glycated proteins in the blood" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"] |
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Allelic Composition: Kmt5btm1a(KOMP)Wtsi/Kmt5btm1a(KOMP)Wtsi Genetic Background: B6JTyr;B6N-Kmt5btm1a(KOMP)Wtsi/Wtsi
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MP:0011966 | abnormal auditory brainstem response waveform shape | "any anomaly in the characteristic pattern of electrical activity recording of a series of vertex positive waves generated by neurons in the ascending auditory system, that can be recorded from scalp electrograms by using computer-averaged responses to short tone bursts" [MGI:csmith] |
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Allelic Composition: Bap1em3Test/Bap1+ Genetic Background: involves: FVB
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MP:0011967 | increased or absent threshold for auditory brainstem response | "increase in the value at which one or more sound frequencies or broadband clicks first elicits a recordable response generated by electrical activity of neurons in the ascending auditory system, or complete lack of a recordable response at any frequency or broadband click" [MGI:csmith] |
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Allelic Composition: Bap1em3Test/Bap1+ Genetic Background: involves: FVB
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