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on page 1 showing 20 out of 2,967 results

Cite this (MGI Cat# 3046320, RRID:MGI:3046320)

Source Database: MGI, catalog # 3046320
Genetic Background: Not Specified
Affected Genes: Myo15
Genomic Alteration: sh2
Availability: Availability unknown check source stock center
Reference: PMID:6889851
Notes: abnormal cochlear hair cell morphology, abnormal tectorial membrane morphology, abnormal utricular macula morphology, abnormal stria vascularis morphology, circling, abnormal cochlear hair cell morphology, organ of Corti degeneration, abnormal organ of Corti morphology, abnormal cochlear ganglion morphology, cochlear ganglion degeneration, deafness, head shaking Allele Detail: Radiation induced

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Cite this (MGI Cat# 2679502, RRID:MGI:2679502)

Source Database: MGI, catalog # 2679502
Genetic Background: Not Specified
Affected Genes: Eif2ak1
Genomic Alteration: tm1Jjch
Availability: Availability unknown check source stock center
Reference: PMID:11726526
Notes: extramedullary hematopoiesis, enlarged heart, abnormal erythrocyte osmotic lysis, macrocytic anemia, abnormal erythropoiesis, increased mean corpuscular volume, abnormal iron homeostasis, abnormal erythrocyte morphology, abnormal erythrocyte physiology, increased number of Heinz bodies, abnormal mean corpuscular hemoglobin Allele Detail: Targeted

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Cite this (MGI Cat# 6193928, RRID:MGI:6193928)

Source Database: MGI, catalog # 6193928
Genetic Background: Not Specified
Affected Genes: Lepr
Genomic Alteration: db
Availability: Availability unknown check source stock center
Reference:
Notes: Allele Detail: Spontaneous

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Cite this (MGI Cat# 5317291, RRID:MGI:5317291)

Source Database: MGI, catalog # 5317291
Genetic Background: Not Specified
Affected Genes: Cntnap1
Genomic Alteration: shm; shm-2J
Availability: Availability unknown check source stock center
Reference:
Notes: abnormal gait, tremors, abnormal motor coordination/balance, ataxia Allele Detail: Spontaneous, Radiation induced

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Cite this (MGI Cat# 2178344, RRID:MGI:2178344)

Source Database: MGI, catalog # 2178344
Genetic Background: Not Specified
Affected Genes: Pde6b
Genomic Alteration: rd1
Availability: Availability unknown check source stock center
Reference: PMID:16576828, PMID:12522242
Notes: absent retinal rod cells, impaired pupillary reflex Allele Detail: Spontaneous

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Cite this (MGI Cat# 3026633, RRID:MGI:3026633)

Source Database: MGI, catalog # 3026633
Genetic Background: Not Specified
Affected Genes:
Genomic Alteration: crf14
Availability: Availability unknown check source stock center
Reference: PMID:12955145
Notes: abnormal craniofacial morphology, microcephaly Allele Detail: Chemically induced (ENU)

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Cite this (MGI Cat# 3575739, RRID:MGI:3575739)

Source Database: MGI, catalog # 3575739
Genetic Background: Not Specified
Affected Genes: Grm5
Genomic Alteration: tm1Fcq
Availability: Availability unknown check source stock center
Reference: PMID:12559117, PMID:11528416
Notes: impaired behavioral response to cocaine, abnormal cocaine consumption, reduced long term potentiation Allele Detail: Targeted

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Cite this (MGI Cat# 3687173, RRID:MGI:3687173)

Source Database: MGI, catalog # 3687173
Genetic Background: Not Specified
Affected Genes: Tyrp1
Genomic Alteration: B-lt
Availability: Availability unknown check source stock center
Reference: PMID:8248019
Notes: decreased endocochlear potential, abnormal inner ear morphology, abnormal hearing physiology, abnormal coat/hair pigmentation, abnormal stria vascularis morphology, abnormal ear physiology, abnormal ear morphology Allele Detail: Spontaneous

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Cite this (MGI Cat# 2673583, RRID:MGI:2673583)

Source Database: MGI, catalog # 2673583
Genetic Background: Not Specified
Affected Genes: l11Jus5
Genomic Alteration: l11Jus5
Availability: Availability unknown check source stock center
Reference: PMID:12955145, PMID:16466971
Notes: failure of chorioallantoic fusion, abnormal extraembryonic tissue morphology, embryonic lethality during organogenesis, complete penetrance Allele Detail: Chemically induced (ENU)

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Cite this (MGI Cat# 3716288, RRID:MGI:3716288)

Source Database: MGI, catalog # 3716288
Genetic Background: Not Specified
Affected Genes:
Genomic Alteration: Wt
Availability: Availability unknown check source stock center
Reference: PMID:5814491
Notes: decreased embryo size, abnormal cochlear ganglion morphology, abnormal nasal placode morphology, abnormal embryo development, embryonic lethality during organogenesis, incomplete penetrance, abnormal inner ear development, abnormal geniculate ganglion morphology, abnormal fourth ventricle morphology, abnormal otic vesicle development, abnormal neural tube morphology, abnormal mitosis, abnormal optic placode morphology, absent optic placodes, spinal cord degeneration, absent endolymphatic duct, embryonic growth retardation, abnormal brain morphology Allele Detail: Spontaneous

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Cite this (MGI Cat# 6118940, RRID:MGI:6118940)

Source Database: MGI, catalog # 6118940
Genetic Background: Not Specified
Affected Genes: Rela, Ptf1a
Genomic Alteration: tm1(cre)Hnak; tm1Rsch
Availability: Availability unknown check source stock center
Reference:
Notes: Allele Detail: Targeted

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Cite this (MGI Cat# 3027224, RRID:MGI:3027224)

Source Database: MGI, catalog # 3027224
Genetic Background: Not Specified
Affected Genes:
Genomic Alteration: nur13
Availability: Availability unknown check source stock center
Reference: PMID:12955145
Notes: ataxia Allele Detail: Chemically induced (ENU)

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Cite this (MGI Cat# 4818789, RRID:MGI:4818789)

Source Database: MGI, catalog # 4818789
Genetic Background: Not Specified
Affected Genes: Dclre1b
Genomic Alteration: tm1Schg
Availability: Availability unknown check source stock center
Reference: PMID:20551906
Notes: decreased embryo size, neonatal lethality Allele Detail: Targeted

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Cite this (MGI Cat# 3769250, RRID:MGI:3769250)

Source Database: MGI, catalog # 3769250
Genetic Background: Not Specified
Affected Genes: Sirt4
Genomic Alteration: tm1Fwa
Availability: Availability unknown check source stock center
Reference: PMID:16959573, PMID:17923681
Notes: no abnormal phenotype detected, no abnormal phenotype detected Allele Detail: Targeted

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Cite this (MGI Cat# 3580779, RRID:MGI:3580779)

Source Database: MGI, catalog # 3580779
Genetic Background: Not Specified
Affected Genes: L3mbtl3
Genomic Alteration: tm1Tmiy
Availability: Availability unknown check source stock center
Reference: PMID:15889154
Notes: perinatal lethality, complete penetrance, anemia, abnormal definitive hematopoiesis Allele Detail: Targeted

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Cite this (MGI Cat# 3042043, RRID:MGI:3042043)

Source Database: MGI, catalog # 3042043
Genetic Background: Not Specified
Affected Genes: Mapk7
Genomic Alteration: tm1Jdl; Tg(Myhca-cre)1Abel
Availability: Availability unknown check source stock center
Reference: PMID:15085193
Notes: no abnormal phenotype detected Allele Detail: Targeted, Transgenic

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Cite this (MGI Cat# 6105929, RRID:MGI:6105929)

Source Database: MGI, catalog # 6105929
Genetic Background: Not Specified
Affected Genes: Acot13
Genomic Alteration: tm1Deco
Availability: Availability unknown check source stock center
Reference: PMID:24072708
Notes: decreased food intake, decreased brown fat cell lipid droplet size, increased lean body mass, abnormal circadian temperature homeostasis, abnormal adaptive thermogenesis, increased respiratory quotient, increased food intake, increased oxygen consumption, increased energy expenditure, increased core body temperature, increased body weight, hyperactivity Allele Detail: Targeted

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Cite this (MGI Cat# 6115299, RRID:MGI:6115299)

Source Database: MGI, catalog # 6115299
Genetic Background: Not Specified
Affected Genes: Gli3, Gli2
Genomic Alteration: Xt; tm1Alj
Availability: Availability unknown check source stock center
Reference:
Notes: Allele Detail: Spontaneous, Targeted

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Cite this (MGI Cat# 3696775, RRID:MGI:3696775)

Source Database: MGI, catalog # 3696775
Genetic Background: Not Specified
Affected Genes: Kat6a
Genomic Alteration: tm1Iki
Availability: Availability unknown check source stock center
Reference: PMID:16702405
Notes: skin edema, abnormal tail morphology, decreased B cell number, lethality throughout fetal growth and development, complete penetrance, absent common myeloid progenitor cells, liver hypoplasia, hemorrhage, pallor, decreased hematopoietic stem cell number, abnormal erythropoiesis, abnormal myelopoiesis, small liver Allele Detail: Targeted

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Cite this (MGI Cat# 5450473, RRID:MGI:5450473)

Source Database: MGI, catalog # 5450473
Genetic Background: Not Specified
Affected Genes: Abcd4
Genomic Alteration: tm1a(EUCOMM)Hmgu
Availability: Availability unknown check source stock center
Reference:
Notes: abnormal response to new environment, abnormal response to tactile stimuli Allele Detail: Targeted

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