C57BL/6N-Kdm5bem2(IMPC)Wtsi/WtsiH
Status | Available to order |
EMMA ID | EM:13527 |
International strain name | C57BL/6N-Kdm5bem2(IMPC)Wtsi/WtsiH |
Alternative name | Kdm5bem2(IMPC)Wtsi (VAAE) |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Kdm5bem2(IMPC)Wtsi |
Gene/Transgene symbol | Kdm5b |
Information from provider
Provider | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | Kdm5bem2(IMPC)Wtsi. Inverted exon KI, reverted to WT via loxP71/loxP66 inversion |
Phenotypic information | Homozygous:data not availableHeterozygous:data not available |
Breeding history | Mosaic crossed with C57BL/6N then intercrossed |
References | None available |
Homozygous fertile | not known |
Homozygous viable | yes |
Homozygous matings required | not known |
Immunocompromised | not known |
Information from EMMA
Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Autosomal recessive non-syndromic intellectual disability / Orphanet_88616
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- abnormal mammary gland development / MGI
- abnormal branching of the mammary ductal tree / MGI
- reduced female fertility / MGI
- female infertility / MGI
- premature death / MGI
- no phenotypic analysis / MGI
- decreased uterus weight / MGI
- decreased circulating estradiol level / MGI
- slow postnatal weight gain / MGI
- mortality/aging / MGI
- neonatal lethality, incomplete penetrance / MGI
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