- abnormal oocyte morphology / MGI
- small ovary / MGI
- impaired ovarian folliculogenesis / MGI
- absent mature ovarian follicles / MGI
- small testis / MGI
- Leydig cell hyperplasia / MGI
- seminiferous tubule degeneration / MGI
- abnormal spermatogenesis / MGI
- increased circulating follicle stimulating hormone level / MGI
- female infertility / MGI
- abnormal ovulation / MGI
- abnormal spermiogenesis / MGI
- asthenozoospermia / MGI
- abnormal spermatogonia proliferation / MGI
- oligozoospermia / MGI
- decreased testis weight / MGI
- decreased male germ cell number / MGI
- abnormal acrosome morphology / MGI
- early reproductive senescence / MGI
C57BL/6N-Taf4bem1(IMPC)Wtsi/WtsiOrl
Status | Available to order |
EMMA ID | EM:13756 |
International strain name | C57BL/6N-Taf4bem1(IMPC)Wtsi/WtsiOrl |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Taf4bem1(IMPC)Wtsi |
Gene/Transgene symbol | Taf4b |
Information from provider
Provider | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from CRISPR zygote microinjection. For further details see the project page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Institut de Transgenose, INTRAGENE, Orléans, France |
Animals used for archiving | heterozygous C57BL/6N |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Male infertility with azoospermia or oligozoospermia due to single gene mutation / Orphanet_399805
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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