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on page 1 showing 20 out of 1,327 results

Cite this (MGI Cat# 4456249, RRID:MGI:4456249)

Source Database: MGI, catalog # 4456249
Genetic Background: involves: 129S/SvEv * C57BL/6J * DBA * MF1
Affected Genes: Ghr, Igf1
Genomic Alteration: tm1Arge
Availability: Availability unknown check source stock center
Reference: PMID:11133160
Notes: decreased width of hypertrophic chondrocyte zone, abnormal trabecular bone morphology, abnormal long bone epiphyseal plate proliferative zone, abnormal chondrocyte morphology, proportional dwarf, postnatal growth retardation, delayed endochondral bone ossification, abnormal long bone hypertrophic chondrocyte zone Allele Detail: Targeted

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Cite this (MGI Cat# 2662461, RRID:MGI:2662461)

Source Database: MGI, catalog # 2662461
Genetic Background: involves: C57BL/6
Affected Genes: Sh2b1
Genomic Alteration: tm1Ayos
Availability: Availability unknown check source stock center
Reference: PMID:11940664
Notes: proportional dwarf, oligozoospermia, ovary hypoplasia, reduced male fertility, reduced female fertility, endocrine/exocrine gland phenotype, abnormal ovulation, testis hypoplasia, decreased testis weight, postnatal growth retardation, asthenozoospermia, abnormal ovarian folliculogenesis, neonatal lethality, incomplete penetrance, abnormal oocyte morphology, abnormal epididymis morphology, immune system phenotype, decreased ovary weight, abnormal uterus development, decreased body weight, Leydig cell hypoplasia Allele Detail: Targeted

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Cite this (MGI Cat# 3801484, RRID:MGI:3801484)

Source Database: MGI, catalog # 3801484
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C3H/HeSn
Affected Genes: Mecp2
Genomic Alteration: tm1Pplt
Availability: Availability unknown check source stock center
Reference: PMID:16467389
Notes: lethargy, weight loss, postnatal growth retardation, premature death, malocclusion Allele Detail: Targeted

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Cite this (MGI Cat# 2174949, RRID:MGI:2174949)

Source Database: MGI, catalog # 2174949
Genetic Background: involves: 129S5/SvEvBrd
Affected Genes: Ednrb
Genomic Alteration: tm1Ywa
Availability: Availability unknown check source stock center
Reference: PMID:8001159, PMID:10496965
Notes: intestinal obstruction, abnormal choroid pigmentation, abnormal coat/hair pigmentation, decreased acute inflammation, hypoalgesia, premature death, cachexia, abnormal hair follicle melanocyte morphology, postnatal growth retardation, white spotting, variable depigmentation, aganglionic megacolon Allele Detail: Targeted

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Cite this (MGI Cat# 5496263, RRID:MGI:5496263)

Source Database: MGI, catalog # 5496263
Genetic Background: involves: BALB/cJ * C57BL/6
Affected Genes: Gt(ROSA)26Sor
Genomic Alteration: tm2.1(CAG-PSTPIP1*)Dtg
Availability: Availability unknown check source stock center
Reference: PMID:23293022
Notes: circling, decreased birth body size, decreased body weight, increased circulating interleukin-1 alpha level, increased circulating interleukin-1 beta level, increased circulating tumor necrosis factor level, integument phenotype, nervous system phenotype, skeleton phenotype, postnatal growth retardation, prenatal lethality, incomplete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 5433858, RRID:MGI:5433858)

Source Database: MGI, catalog # 5433858
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Affected Genes: Slc4a4
Genomic Alteration: tm1.1Slin
Availability: Availability unknown check source stock center
Reference: PMID:21228764
Notes: increased circulating renin level, decreased gastrocnemius weight, decreased urine pH, abnormal urine homeostasis, postnatal growth retardation, decreased hemoglobin content, decreased kidney weight, edema, increased urine sodium level, increased long bone epiphyseal plate size, increased circulating aldosterone level, uremia, dilated renal tubules, decreased urine osmolality, decreased length of long bones, renal tubular acidosis, abnormal skeleton morphology, abnormal renal tubule epithelium morphology, reticulocytosis, metabolic acidosis, abnormal blood homeostasis, renal tubule atrophy, acidemia, corneal opacity, abnormal intestine physiology, abnormal intestine morphology, acidosis, postnatal lethality, complete penetrance, decreased body size, increased urine calcium level, increased circulating calcium level, abnormal blood circulation, abnormal renal reabsorbtion, anemia, enlarged spleen, increased spleen weight, abnormal compact bone morphology Allele Detail: Targeted

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Cite this (MGI Cat# 3590544, RRID:MGI:3590544)

Source Database: MGI, catalog # 3590544
Genetic Background: involves: 129S1/Sv * C57BL/6J
Affected Genes: Cux1
Genomic Alteration: tm1Rhsc
Availability: Availability unknown check source stock center
Reference: PMID:11739170
Notes: decreased body size, decreased double-positive T cell number, cachexia, decreased total body fat amount, abnormal bone structure, abnormal tumor necrosis factor level, small thymus, neonatal lethality, incomplete penetrance, abnormal hair follicle morphology, postnatal growth retardation, decreased B cell number, thymus hypoplasia, thymus cortex hypoplasia, premature death, increased hair follicle number, alopecia, wavy vibrissae, abnormal myelopoiesis, abnormal T cell differentiation, decreased thymocyte number Allele Detail: Targeted

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Cite this (MGI Cat# 6120559, RRID:MGI:6120559)

Source Database: MGI, catalog # 6120559
Genetic Background: B6(Cg)-Gt(ROSA)26Sor
Affected Genes: Gt(ROSA)26Sor
Genomic Alteration: tm1.1(DUX4*)Plj
Availability: Availability unknown check source stock center
Reference: PMID:29415061
Notes: enlarged lymph nodes, muscle phenotype, decreased body weight, enlarged popliteal lymph nodes, alopecia, postnatal growth retardation Allele Detail: Targeted

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Cite this (MGI Cat# 3612255, RRID:MGI:3612255)

Source Database: MGI, catalog # 3612255
Genetic Background: involves: 129S1/Sv * 129X1/SvJ
Affected Genes: Gria2
Genomic Alteration: tm2Rsp
Availability: Availability unknown check source stock center
Reference: PMID:10195181
Notes: lethargy, abnormal excitatory postsynaptic potential, postnatal lethality, complete penetrance, postnatal growth retardation, decreased body weight, abnormal hippocampus CA3 region morphology, abnormal AMPA-mediated synaptic currents Allele Detail: Targeted

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Cite this (MGI Cat# 3521740, RRID:MGI:3521740)

Source Database: MGI, catalog # 3521740
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Satb1
Genomic Alteration: tm1Kos
Availability: Availability unknown check source stock center
Reference: PMID:10716941
Notes: small lymph nodes, postnatal lethality, complete penetrance, decreased body size, limb grasping, decreased thymocyte number, abnormal T cell differentiation, abnormal T cell proliferation, small thymus, postnatal growth retardation, arrested T cell differentiation, delayed eyelid opening, small spleen Allele Detail: Targeted

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Cite this (MGI Cat# 3640190, RRID:MGI:3640190)

Source Database: MGI, catalog # 3640190
Genetic Background: C3.Cg-Reln
Affected Genes: Reln
Genomic Alteration: rl
Availability: Availability unknown check source stock center
Reference: PMID:7127145, PMID:4644329
Notes: abnormal stratification in cerebral cortex, abnormal dentate gyrus morphology, abnormal cerebral cortex morphology, abnormal hippocampus morphology, abnormal olfactory cortex morphology, abnormal entorhinal cortex morphology, abnormal neuronal migration, abnormal sensory neuron innervation pattern, slow postnatal weight gain, ataxia, behavior/neurological phenotype, postnatal growth retardation, abnormal hippocampus CA1 region morphology, diarrhea, premature death, abnormal hippocampus CA2 region morphology Allele Detail: Spontaneous

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Cite this (MGI Cat# 3037643, RRID:MGI:3037643)

Source Database: MGI, catalog # 3037643
Genetic Background: involves: BALB/cAnBomUrd
Affected Genes: Phex
Genomic Alteration: Hyp-Duk
Availability: Availability unknown check source stock center
Reference: PMID:15029877
Notes: abnormal hindlimb morphology, circling, postnatal growth retardation, short tail Allele Detail: Spontaneous

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Cite this (MGI Cat# 5811453, RRID:MGI:5811453)

Source Database: MGI, catalog # 5811453
Genetic Background: involves: 129 * C57BL/6
Affected Genes: Gnptab
Genomic Alteration: tm1Dkji
Availability: Availability unknown check source stock center
Reference: PMID:26857995
Notes: decreased body size, increased interleukin-6 secretion, postnatal growth retardation, kyphosis, abnormal cell morphology, decreased bone mineral density, abnormal chondrocyte morphology, increased lysosomal enzyme secretion, decreased body length, abnormal salivary gland morphology, decreased body weight, coarse facial features, decreased bone mineral content, decreased bone mass, abnormal lysosome morphology Allele Detail: Targeted

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Cite this (MGI Cat# 3640353, RRID:MGI:3640353)

Source Database: MGI, catalog # 3640353
Genetic Background: involves: 129S7/SvEvBrd * C57BL/6J
Affected Genes: Ggt1, Ggt5
Genomic Alteration: tm1Zuk; tm1Mwl
Availability: Availability unknown check source stock center
Reference: PMID:11463821
Notes: cataract, premature death, reduced fertility, abnormal sexual maturation, abnormal coat/hair pigmentation, postnatal growth retardation Allele Detail: Targeted

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Cite this (MGI Cat# 5009418, RRID:MGI:5009418)

Source Database: MGI, catalog # 5009418
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA
Affected Genes: Ilk
Genomic Alteration: Tg(KRT14-cre)1Amc; tm1Star
Availability: Availability unknown check source stock center
Reference: PMID:18234842
Notes: acanthosis, blistering, decreased hair follicle number, skin edema, scaly skin, postnatal growth retardation, decreased keratinocyte proliferation, abnormal skin pigmentation, skin inflammation, thin skin, postnatal lethality, complete penetrance, abnormal epidermal layer morphology, abnormal hair follicle development, abnormal hair follicle physiology, abnormal hair growth, decreased skin tensile strength Allele Detail: Transgenic, Targeted

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Cite this (MGI Cat# 3620910, RRID:MGI:3620910)

Source Database: MGI, catalog # 3620910
Genetic Background: involves: 129S1/Sv * C57BL/6
Affected Genes: Lmna
Genomic Alteration: tm1Stw
Availability: Availability unknown check source stock center
Reference: PMID:14996939, PMID:15608054
Notes: azoospermia, premature death, muscle weakness, postnatal growth retardation, small seminiferous tubules, arrest of male meiosis, small testis Allele Detail: Targeted

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Cite this (MGI Cat# 3043296, RRID:MGI:3043296)

Source Database: MGI, catalog # 3043296
Genetic Background: involves: 129/Sv * C57BL/6
Affected Genes: Mapt
Genomic Alteration: tm1(Mecp2)Jae
Availability: Availability unknown check source stock center
Reference: PMID:15069197
Notes: cachexia, disheveled coat, tremors, excessive scratching, impaired balance, postnatal growth retardation, mortality/aging, abnormal sexual interaction, cataract, ataxia Allele Detail: Targeted

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Cite this (MGI Cat# 5499855, RRID:MGI:5499855)

Source Database: MGI, catalog # 5499855
Genetic Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N
Affected Genes: Wwox
Genomic Alteration: tm2.1Ria
Availability: Availability unknown check source stock center
Reference: PMID:23254685
Notes: decreased trabecular bone connectivity density, decreased bone mineral density, decreased trabecular bone volume, hypoglycemia, decreased bone trabecula number, abnormal trabecular bone morphology, postnatal lethality, complete penetrance, abnormal compact bone morphology, decreased compact bone area, decreased body weight, postnatal growth retardation, increased skeletal tumor incidence, decreased compact bone thickness Allele Detail: Targeted

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Cite this (MGI Cat# 3793277, RRID:MGI:3793277)

Source Database: MGI, catalog # 3793277
Genetic Background: DL-Atp7b
Affected Genes: Atp7b
Genomic Alteration: tx
Availability: Availability unknown check source stock center
Reference: PMID:6863890, PMID:8040371, PMID:11085952, PMID:2845190
Notes: decreased body weight, ataxia, increased liver copper level, decreased liver copper level, abnormal muscle physiology, decreased circulating copper level, liver cirrhosis, curly vibrissae, postnatal growth retardation, postnatal lethality, complete penetrance, increased brain copper level, increased liver copper level, abnormal mineral level, disheveled coat, abnormal hepatocyte morphology, abnormal copper level, increased kidney copper level, maternal effect, endocrine/exocrine gland phenotype, hypopigmentation, reduced female fertility, tremors, diluted coat color, increased circulating copper level, increased liver copper level Allele Detail: Spontaneous

  • From Current Category

Cite this (MGI Cat# 4399080, RRID:MGI:4399080)

Source Database: MGI, catalog # 4399080
Genetic Background: B6.129S6-Gcg
Affected Genes: Gcg
Genomic Alteration: tm1Yhys
Availability: Availability unknown check source stock center
Reference: PMID:19819987
Notes: digestive/alimentary phenotype, abnormal pancreatic alpha cell morphology, postnatal growth retardation, premature death, improved glucose tolerance, increased circulating glucose level, increased pancreatic islet number, increased body weight, increased body length, increased pancreas weight, increased insulin sensitivity, polyuria, decreased circulating insulin level Allele Detail: Targeted

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