Strain Information | |
|---|---|
| Image | |
| BRC No. | RBRC05431 |
| Type | Targeted Mutation |
| Species | Mus musculus |
| Strain name | C57BL/6-Ano5<tm1Itak> |
| Former Common name | |
| H-2 Haplotype | |
| ES Cell line | |
| Background strain | C57BL/6JJcl |
| Appearance | |
| Strain development | Developed by Hiroshi Inoue, Satoshi Tsutsumi, Mitsuo Itakura, Institute for Genome Research, The University of Tokushima and Kuniko Mizuta, Hiroshima University Graduate School of Biomedical Sciences. A neomycin selection cassette was transferred into C57BL/6 derived ES cells to replace exon 1 of Ano5 gene. |
| Strain description | Ano5, anoctamin 5 (Gdd1) knockout mice. The first exon of Ano5 gene was replaced with a neomycin selection cassette. Homozygous mutant mice show no obvious abnormality. |
| Colony maintenance | |
| References | Autosomal dominant gnathodiaphyseal dysplasia maps to chromosome 11p14.3-15.1. Satoshi Tsutsumi, Nobuyuki Kamata, Yutaka Maruoka, Miki Ando, Osamu Tezuka, Shoji Enomoto, Ken Omura, Masaru Nagayama, Eiji Kudo, Maki Moritani, Takashi Yamaoka, Mitsuo Itakura J. Bone Miner. Res., 18, 413-418 (2003). 12619924The novel gene encoding a putative transmembrane protein is mutated in gnathodiaphyseal dysplasia (GDD). Satoshi Tsutsumi, Nobuyuki Kamata, Tamara J Vokes, Yutaka Maruoka, Koichi Nakakuki, Shoji Enomoto, Ken Omura, Teruo Amagasa, Masaru Nagayama, Fumiko Saito-Ohara, Johji Inazawa, Maki Moritani, Takashi Yamaoka, Hiroshi Inoue, Mitsuo Itakura Am. J. Hum. Genet., 74, 1255-1261 (2004). 15124103Molecular cloning and characterization of the murine gnathodiaphyseal dysplasia gene GDD1. Satoshi Tsutsumi, Hiroshi Inoue, Yukiko Sakamoto, Kuniko Mizuta, Nobuyuki Kamata, Mitsuo Itakura Biochem. Biophys. Res. Commun., 331, 1099-1106 (2005). 15882990Molecular characterization of GDD1/TMEM16E, the gene product responsible for autosomal dominant gnathodiaphyseal dysplasia. Kuniko Mizuta, Satoshi Tsutsumi, Hiroshi Inoue, Yukiko Sakamoto, Katsutoshi Miyatake, Katsuyuki Miyawaki, Sumihare Noji, Nobuyuki Kamata, Mitsuo Itakura Biochem. Biophys. Res. Commun., 357, 126-132 (2007). 17418107Recessive mutations in the putative calcium-activated chloride channel Anoctamin 5 cause proximal LGMD2L and distal MMD3 muscular dystrophies. Véronique Bolduc, Gareth Marlow, Kym M Boycott, Khalil Saleki, Hiroshi Inoue, Johan Kroon, Mitsuo Itakura, Yves Robitaille, Lucie Parent, Frank Baas, Kuniko Mizuta, Nobuyuki Kamata, Isabelle Richard, Wim H J P Linssen, Ibrahim Mahjneh, Marianne de Visser, Rumaisa Bashir, Bernard Brais Am. J. Hum. Genet., 86, 213-221 (2010). 20096397 |
Health Report | |
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| Examination Date / Room / Rack | |
Gene | |||||||
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| Gene Symbol | Gene Name | Chr. | Allele Symbol | Allele Name | Common Names | Promoter | Diseases Related to This Gene |
| Ano5 MGI:3576659 | anoctamin 5 | 7 | Ano5 <tm1Itak> | targeted mutation 1, Mitsuo Itakura | |||
| neo | neomycin resistance gene (E. coli) | 7 | mouse phosphoglycerate kinase promoter (PGK promoter) | ||||
Phenotype | |
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| Phenotype annotation from literatures by Mammalian phenotype ontology | |
| Detailed phenotype data | |
Ordering Information | |
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| Donor DNA | mouse phosphoglycerate kinase promoter (PGK promoter), E. coli. neo, mouse GDD1 (ANO5) genomic DNA |
| Research application | Mouse Models for Human Disease |
| Specific Term and Conditions | The availability of the BIOLOGICAL RESOURCE is limited to a RECIPIENT of a not-for profit institution for a not-for-profit research. In publishing the research results obtained by use of the BIOLOGICAL RESOURCE, an acknowledgment to the DEPOSITOR is requested. |
| Depositor | Mitsuo Itakura (Tokushima University) |
| Strain Status | Frozen embryos Frozen sperm |
| Strain Availability | Recovered litters from cryopreserved embryos (2 to 4 months) Cryopreserved sperm (within 1 month) Cryopreserved embryos (within 1 month) |
| Additional Info. | Necessary documents for ordering:
Genotyping protocol -PCR- |
BRC mice in Publications |
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Xu J, El Refaey M, Xu L, Zhao L, Gao Y, Floyd K, Karaze T, Janssen PM, Han R. Genetic disruption of Ano5 in mice does not recapitulate human ANO5-deficient muscular dystrophy. Skelet Muscle 5 43(2015) 26693275 |