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on page 1 showing 7 out of 7 results

Cite this (MGI Cat# 3617782, RRID:MGI:3617782)

Source Database: MGI, catalog # 3617782
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Ctnnb1
Genomic Alteration: tm2Wbm
Availability: Availability unknown check source stock center
Reference:
Notes: Allele Detail: Targeted

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Cite this (MGI Cat# 3706573, RRID:MGI:3706573)

Source Database: MGI, catalog # 3706573
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Ctnnb1
Genomic Alteration: tm1(Nfkbia)Rsu
Availability: Availability unknown check source stock center
Reference: PMID:11585809
Notes: prenatal lethality, complete penetrance Allele Detail: Targeted

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Cite this (MGI Cat# 2674150, RRID:MGI:2674150)

Source Database: MGI, catalog # 2674150
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Ctnnb1
Genomic Alteration: tm2Wbm
Availability: Availability unknown check source stock center
Reference: PMID:10662781
Notes: abnormal germ layer development, absent mesoderm, embryonic lethality during organogenesis, complete penetrance, decreased embryo size, abnormal rostral-caudal axis patterning, abnormal ectoderm development, abnormal gastrulation, abnormal mesoderm development, abnormal proximal-distal axis patterning, failure to gastrulate, abnormal developmental patterning Allele Detail: Targeted

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Cite this (MGI Cat# 2674160, RRID:MGI:2674160)

Source Database: MGI, catalog # 2674160
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Ctnnb1
Genomic Alteration: tm3Wbm
Availability: Availability unknown check source stock center
Reference: PMID:10662781
Notes: failure to gastrulate, absent mesoderm, abnormal ectoderm development, abnormal developmental patterning, abnormal rostral-caudal axis patterning, abnormal gastrulation, abnormal mesoderm development, abnormal proximal-distal axis patterning, abnormal germ layer development, embryonic lethality during organogenesis, complete penetrance, decreased embryo size Allele Detail: Targeted

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Cite this (MGI Cat# 2673243, RRID:MGI:2673243)

Source Database: MGI, catalog # 2673243
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Ctnnb1
Genomic Alteration: tm4Wbm; Tg(Pou3f4-cre)32Cren
Availability: Availability unknown check source stock center
Reference: PMID:12798297
Notes: abnormal nervous system morphology, decreased spinal cord size, decreased brain size, abnormal brain morphology Allele Detail: Transgenic, Targeted

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Cite this (MGI Cat# 3706574, RRID:MGI:3706574)

Source Database: MGI, catalog # 3706574
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Ctnnb1
Genomic Alteration: tm1(Nfkbia)Rsu
Availability: Availability unknown check source stock center
Reference: PMID:11585809
Notes: abnormal nitric oxide homeostasis, small molars, abnormal macrophage physiology, abnormal peripheral lymph node morphology, abnormal intestinal goblet cell morphology, narrow eye opening, dry eyes, small Peyer's patches, liver hemorrhage, lethargy, decreased Peyer's patch number, kinked tail, tremors, misaligned incisors, increased susceptibility to parasitic infection, sparse vibrissae, increased susceptibility to otitis media, abnormal corneal epithelium morphology, abnormal corneal stroma morphology, keratoconjunctivitis sicca, Harderian gland atrophy, abnormal eye morphology, abnormal eyelid margin morphology, increased hepatocyte apoptosis, increased granulocyte number, increased leukocyte cell number, impaired balance, hunched posture, growth retardation of molars, growth retardation of incisors, short incisors, increased inflammatory response, small axillary lymph nodes, small brachial lymph nodes, abnormal cervical lymph node morphology, premature death, abnormal foot pad morphology, abnormal coat appearance, gastrointestinal hemorrhage, early eyelid opening, domed cranium, decreased litter size, decreased hair follicle number, decreased body size, deafness, conjunctivitis, blindness, alopecia, absent Meibomian glands, absent peripheral lymph nodes, prenatal lethality, incomplete penetrance, absent hair follicles, abnormal hair follicle development, absent Peyer's patches, abnormal vibrissa follicle morphology, abnormal sweat gland morphology, increased hair follicle apoptosis, abnormal hair growth, abnormal coat/ hair morphology, abnormal small intestine morphology, absent popliteal lymph nodes Allele Detail: Targeted

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Cite this (MGI Cat# 2674138, RRID:MGI:2674138)

Source Database: MGI, catalog # 2674138
Genetic Background: involves: 129P2/OlaHsd * C57BL/6
Affected Genes: Ctnnb1
Genomic Alteration: tm1Wbm
Availability: Availability unknown check source stock center
Reference: PMID:10662781
Notes: abnormal gastrulation, absent mesoderm, failure to gastrulate, abnormal rostral-caudal axis patterning, decreased embryo size, embryonic lethality during organogenesis, complete penetrance, abnormal ectoderm development, abnormal germ layer development, abnormal developmental patterning, abnormal mesoderm development, abnormal proximal-distal axis patterning Allele Detail: Targeted

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