Strain Data Sheet

RBRC00330

Strain Information

Image
BRC No.RBRC00330
TypeTargeted Mutation and Spontaneous Mutation CongenicCartagena
SpeciesMus musculus
Strain nameC.Cg-Tnc<tm1Sia> Foxn1<nu> Hspa9a<C3H/HeN>/Rbrc
Former Common nameBALB/cA-Tnc<tm1Sia>-nude-CSA; BALB/cA-TgH(Tnc)-Foxn1nu-CSA
H-2 Haplotype
ES Cell line
Background strainBALB/cA
Appearance
Strain development
Strain description
Colony maintenance
References
A novel methodology for analysis of cell distribution in chimeric mouse organs using a strain specific antibody.
Kusakabe M, Yokoyama M, Sakakura T, Nomura T, Hosick H L, Nishizuka Y
J. Cell. Biol., 107, 257-265 (1988). 3292542

Murine tenascin: cDNA cloning, structure and temporal expression of isoforms.
Saga Y, Tsukamoto T, Jing N, Kusakabe M, Sakakura T
Gene, 104, 177-185 (1991). 1717349

Mice develop normally without tenascin.
Saga Y, Yagi T, Ikawa Y, Sakakura T, Aizawa S
Genes Dev., 6, 1821-1831 (1992). 1383086

The mouse chimera during intrauterine stages: immunohistochemical analysis with the C3H strain-specific antibody.
Yoshiki A, Sakakura T, Kusakabe M
J. Histochem. Cytochem., 41, 1583-1590 (1993). 8245417

Antigenic protein specific for C3H strain mouse is a mitochondrial stress-70 protein.
Michikawa Y, Baba T, Arai Y, Sakakura T, Tanaka M, Kusakabe M
Biochem. Biophys. Res. Commun., 196, 223-232 (1993). 7692847

Tenascin knockout mice: barrels, boundary molecules, and glial scars.
Steindler D A, Settles D, Erickson H P, Laywell E D, Yoshiki A, Faissner A, Kusakabe M
J. Neurosci., 15, 1971-1983 (1995). 7534342

Abnormal behavior and neurotransmissions of tenascin gene knockout mouse.
Fukamauchi F, Mataga N, Wang Y J, Sato S, Youshiki A, Kusakabe M
Biochem. Biophys. Res. Commun., 221, 151-156 (1996). 8660327

乳癌基礎研究, 5, 41-45 (1996).

炎症, 15(5), 377-381 (1996).

Tyrosine hydroxylase activity and its mRNA level in dopaminergic neurons of tenascin gene knockout mouse.
Fukamauchi F, Mataga N, Wang Y J, Sato S, Yoshiki A, Kusakabe M
Biochem. Biophys. Res. Commun., 231, 356-359 (1997). 9070278
more 8 references
Effect of tenascin-C deficiency on chemically induced dermatitis in the mouse.
Koyama Y, Kusubata M, Yoshiki A, Hiraiwa N, Ohashi T, Irie S, Kusakabe M
J. Invest. Dermatol., 111, 930-935 (1998). 9856798

Tenascin-C promotes healing of Habu-snake venom-induced glomerulonephritis: studies in knockout congenic mice and in culture.
Nakao N, Hiraiwa N, Yoshiki A, Ike F, Kusakabe M
Am. J. Pathol., 152, 1237-1245 (1998). 9588892

22nd Congress of the International Association for Breast Cancer Research Athens, Greece 25-28 September, pp 197-201 (1998). 9863494

Corneal wound healing in tenascin knockout mouse.
Matsuda A, Yoshiki A, Tagawa Y, Matsuda H, Kusakabe M
Invest. Ophthalmol. Visual. Sci., 40, 1071-1080 (1999). 10235540

乳癌基礎研究, 8, 26-31 (1999).

Loss of cortical and thalamic neuronal tenascin-C expression in a transgenic mouse expressing exon 1 of the human Huntington disease gene.
Kusakabe M, Mangiarini L, Laywell E D, Bates G P, Yoshiki A, Hiraiwa N, Inoue J, Steindler D A
J. Comp. Neurol., 430, 485-500 (2001). 11169482

PDGF receptor-alpha deficiency in glomerular mesangial cells of tenascin-C knockout mice.
Matsumoto K, Hiraiwa N, Yoshiki A, Ohnishi M, Kusakabe M
Biochem. Biophys. Res. Commun., 290, 1220-1227 (2002). 11811993

Tenascin-C expression and splice variant in habu snake venom-induced glomerulonephritis.
Matsumoto K, Hiraiwa N, Yoshiki A, Ohnishi M, Kusakabe M
Exp. Mol. Pathol., 72, 186-195 (2002). 12009782

Health Report

Examination Date / Room / Rack

Gene

Gene SymbolGene NameChr.Allele SymbolAllele NameCommon NamesPromoterDiseases Related to This Gene
Foxn1
MGI:102949		forkhead box N111Foxn1<nu>
MGI:1856108		nude
  • T-cell immunodeficiency, congenital alopecia, and nail dystrophy(DisGeNET, MedGEN)

  • T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominant(MedGEN)
    • Hspa9a
    MGI:96245    		heat shock protein, A18Hspa9a<C3H/HeN>
  • autosomal dominant sideroblastic anemia(MedGEN)

  • even-plus syndrome(MedGEN)
    • Tnc
    MGI:101922    		tenascin C4Tnc<tm1Sia>
    MGI:2148540    		targeted mutation 1, Shinichi Aizawa
  • autosomal dominant nonsyndromic hearing loss 56(MedGEN)
    • lacZ beta-galactosidase (E. coli)4
    neo neomycin resistance gene (E. coli)4 mouse phosphoglycerate kinase promoter (PGK promoter)

    Phenotype

    Annotation by Mammalian phenotyhpe ontology
  • abnormal CNS synaptic transmission(MP:0002206)

  • abnormal Peyer's patch germinal center morphology(MP:0002391)

  • abnormal T cell activation(MP:0001828)

  • abnormal circadian behavior(MP:0020467)

  • abnormal circulating cytokine level(MP:0010210)
    • more 89 phenotypes
  • abnormal circulating gonadotropin level(MP:0003361)

  • abnormal coat/ hair morphology(MP:0000367)

  • abnormal compact bone morphology(MP:0003797)

  • abnormal corneocyte morphology(MP:0030605)

  • abnormal cutaneous collagen fibril morphology(MP:0008438)

  • abnormal embryonic tissue morphology(MP:0002085)

  • abnormal epidermal layer morphology(MP:0001216)

  • abnormal epidermis stratum basale morphology(MP:0001231)

  • abnormal epidermis stratum corneum morphology(MP:0001240)

  • abnormal epidermis stratum granulosum morphology(MP:0001239)

  • abnormal estrous cycle(MP:0001927)

  • abnormal hair cortex keratinization(MP:0009801)

  • abnormal hair cortex morphology(MP:0003811)

  • abnormal hair cuticle(MP:0003810)

  • abnormal hair follicle inner root sheath morphology(MP:0010685)

  • abnormal hair follicle morphology(MP:0000377)

  • abnormal hair shaft morphology(MP:0003809)

  • abnormal liver morphology(MP:0000598)

  • abnormal lymph node T cell domain morphology(MP:0002347)

  • abnormal lymph node morphology(MP:0002339)

  • abnormal muscle morphology(MP:0002108)

  • abnormal nail matrix morphology(MP:0012405)

  • abnormal nail morphology(MP:0000579)

  • abnormal nail plate morphology(MP:0012403)

  • abnormal serotonin level(MP:0005322)

  • abnormal spleen morphology(MP:0000689)

  • abnormal spleen physiology(MP:0008737)

  • abnormal splenic cell ratio(MP:0008826)

  • abnormal thymus development(MP:0000704)

  • abnormal thymus epithelium morphology(MP:0009544)

  • abnormal thymus morphology(MP:0000703)

  • abnormal trabecular bone morphology(MP:0000130)

  • abnormal venule morphology(MP:0004125)

  • absent vibrissae(MP:0001284)

  • ascites(MP:0005324)

  • asthenozoospermia(MP:0002675)

  • athymia(MP:0000705)

  • blepharitis(MP:0005251)

  • chromosomal instability(MP:0008866)

  • coiled sperm flagellum(MP:0009238)

  • cornea vascularization(MP:0005542)

  • decreased T cell number(MP:0005018)

  • decreased body size(MP:0001265)

  • decreased body weight(MP:0001262)

  • decreased circulating alanine transaminase level(MP:0002942)

  • decreased circulating follicle stimulating hormone level(MP:0002790)

  • decreased circulating interleukin-2 level(MP:0008600)

  • decreased circulating interleukin-6 level(MP:0008597)

  • decreased circulating luteinizing hormone level(MP:0002773)

  • decreased circulating tumor necrosis factor level(MP:0008554)

  • decreased dopamine level(MP:0005643)

  • decreased interferon-gamma secretion(MP:0008567)

  • decreased leukocyte cell number(MP:0000221)

  • decreased lymphocyte cell number(MP:0005016)

  • decreased skeletal muscle fiber size(MP:0009400)

  • decreased skeletal muscle mass(MP:0004819)

  • decreased susceptibility to bacterial infection(MP:0002411)

  • decreased susceptibility to parasitic infection(MP:0005026)

  • decreased thymocyte number(MP:0000715)

  • deformed nails(MP:0000580)

  • endocrine/exocrine gland phenotype(MP:0005379)

  • female infertility(MP:0001926)

  • hairless(MP:0003815)

  • hearing/vestibular/ear phenotype(MP:0005377)

  • hyperactivity(MP:0001399)

  • impaired spatial learning(MP:0012307)

  • impaired swimming(MP:0001522)

  • increased bone mineral density(MP:0000062)

  • increased incidence of corneal inflammation(MP:0001313)

  • increased length of allograft survival(MP:0004751)

  • increased plasmacytoma incidence(MP:0010286)

  • increased stereotypic behavior(MP:0001409)

  • increased susceptibility to viral infection induced morbidity/mortality(MP:0009791)

  • increased susceptibility to viral infection(MP:0002418)

  • increased thymocyte apoptosis(MP:0009541)

  • infertility(MP:0001924)

  • nail dystrophy(MP:0012400)

  • postnatal growth retardation(MP:0001732)

  • postnatal lethality, incomplete penetrance(MP:0011086)

  • premature death(MP:0002083)

  • reduced hair shaft melanin granule number(MP:0008732)

  • reduced male fertility(MP:0001922)

  • short nails(MP:0012399)

  • short vibrissae(MP:0001282)

  • small ovary(MP:0001127)

  • small spleen(MP:0000692)

  • small thymus(MP:0000706)

  • thin skin(MP:0001199)

  • wavy vibrissae(MP:0001279)
    • Detailed phenotype data

    Ordering Information

    Donor DNAE. coli lacZ, mouse phosphoglycerate kinase promoter (PGK promoter), E. coli neo, mouse tenascin genomic DNA
    Research applicationCancer Research
    Cell Biology Research
    Specific Term and ConditionsIn publishing the research results obtained by use of the BIOLOGICAL RESOURCE, a citation of the following literature(s) designated by the DEPOSITOR is requested. J. Cell. Biol., 107, 257-265 (1988). J. Histochem. Cytochem, 41, 1583-1590 (1993). Biochem. Biophys. Res. Commun., 196, 223-232 (1993). Am. J. Pathol., 152, 1237-1245 (1998). J. Invest. Dermatol., 111, 930-935 (1998). Invest. Ophthalmol. Visual. Sci., 40, 40, 1071-1080 (1999).
    DepositorRIKEN BRC (RIKEN BRC)
    Strain Statusan icon for Frozen embryosFrozen embryos
    Strain AvailabilityRecovered litters from cryopreserved embryos (2 to 4 months)
    Additional Info.Necessary documents for ordering:
    1. Order form (Japanese / English)
    2. Category I MTA: MTA for distribution with RIKEN BRC (Japanese / English)
    3. Acceptance of responsibility for living modified organism (Japanese / English)

    BRC mice in Publications

    No Data