- decreased bone mineral density / IMPC
- abnormal cranium morphology / IMPC
- abnormal snout morphology / IMPC
- abnormal mandible morphology / IMPC
- decreased body length / IMPC
- decreased body weight / IMPC
- abnormal tooth morphology / IMPC
- abnormal joint morphology / IMPC
- decreased lean body mass / IMPC
- vertebral fusion / IMPC
- abnormal incisor morphology / IMPC
- absent pinna reflex / IMPC
- decreased total body fat amount / IMPC
- decreased bone mineral content / IMPC
B6Brd;B6N-Tyrc-Brd Slc25a21tm1a(KOMP)Wtsi/Wtsi
Status | Available to order |
EMMA ID | EM:12127 |
International strain name | B6Brd;B6N-Tyrc-Brd Slc25a21tm1a(KOMP)Wtsi/Wtsi |
Alternative name | EPD0085_1_D04 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Slc25a21tm1a(KOMP)Wtsi |
Gene/Transgene symbol | Slc25a21 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
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Information from provider
Provider | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from KOMP ES clone EPD0085_1_D04. For further details on the construction of this clone see the page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References |
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Information from EMMA
Archiving centre | Wellcome Trust Sanger Institute, Hinxton, United Kingdom |
Animals used for archiving | heterozygous C57BL/6Brd-Tyr |
Disease and phenotype information
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- decreased circulating magnesium level / IMPC
- decreased body weight / IMPC
- abnormal mandible morphology / IMPC
- abnormal tooth morphology / IMPC
- abnormal cranium morphology / IMPC
- decreased lean body mass / IMPC
- increased total body fat amount / IMPC
- decreased body length / IMPC
- abnormal snout morphology / IMPC
- abnormal joint morphology / IMPC
- decreased bone mineral density / IMPC
- decreased bone mineral content / IMPC
- vertebral fusion / IMPC
- abnormal incisor morphology / IMPC
- decreased mean corpuscular hemoglobin / IMPC
- decreased total body fat amount / IMPC
- absent pinna reflex / IMPC
- decreased mean corpuscular volume / IMPC
MGI phenotypes (allele matching)
- decreased circulating LDL cholesterol level / MGI
- abnormal cranium morphology / MGI
- abnormal snout morphology / MGI
- abnormal mandible morphology / MGI
- decreased body length / MGI
- decreased body weight / MGI
- abnormal tooth morphology / MGI
- abnormal joint morphology / MGI
- decreased circulating alanine transaminase level / MGI
- abnormal incisor morphology / MGI
- decreased circulating potassium level / MGI
- decreased circulating aspartate transaminase level / MGI
- absent pinna reflex / MGI
- decreased total body fat amount / MGI
- decreased bone mineral content / MGI
MGI phenotypes (gene matching)
- decreased circulating LDL cholesterol level / MGI
- abnormal cranium morphology / MGI
- abnormal snout morphology / MGI
- abnormal mandible morphology / MGI
- decreased body length / MGI
- decreased body weight / MGI
- abnormal tooth morphology / MGI
- abnormal joint morphology / MGI
- decreased circulating alanine transaminase level / MGI
- abnormal incisor morphology / MGI
- decreased circulating potassium level / MGI
- decreased circulating aspartate transaminase level / MGI
- absent pinna reflex / MGI
- decreased total body fat amount / MGI
- decreased bone mineral content / MGI
Literature references
- Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes.;White Jacqueline K, Gerdin Anna-Karin, Karp Natasha A, Ryder Ed, Buljan Marija, Bussell James N, Salisbury Jennifer, Clare Simon, Ingham Neil J, Podrini Christine, Houghton Richard, Estabel Jeanne, Bottomley Joanna R, Melvin David G, Sunter David, Adams Niels C, null null, Tannahill David, Logan Darren W, Macarthur Daniel G, Flint Jonathan, Mahajan Vinit B, Tsang Stephen H, Smyth Ian, Watt Fiona M, Skarnes William C, Dougan Gordon, Adams David J, Ramirez-Solis Ramiro, Bradley Allan, Steel Karen P, ;2013;Cell;154;452-64; 23870131
- Targeting of Slc25a21 is associated with orofacial defects and otitis media due to disrupted expression of a neighbouring gene.;Maguire Simon, Estabel Jeanne, Ingham Neil, Pearson Selina, Ryder Edward, Carragher Damian M, Walker Nicolas, null null, Bussell James, Chan Wai-In, Keane Thomas M, Adams David J, Scudamore Cheryl L, Lelliott Christopher J, Ramírez-Solis Ramiro, Karp Natasha A, Steel Karen P, White Jacqueline K, Gerdin Anna-Karin, ;2014;PloS one;9;e91807; 24642684
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