- small salivary gland / MGI
- abnormal adrenal gland morphology / MGI
- abnormal sex gland morphology / MGI
- abnormal female reproductive system morphology / MGI
- small ovary / MGI
- abnormal ovarian follicle morphology / MGI
- absent mature ovarian follicles / MGI
- absent corpus luteum / MGI
- abnormal vagina epithelium morphology / MGI
- abnormal vagina orifice morphology / MGI
- abnormal male reproductive system morphology / MGI
- abnormal spermatogenesis / MGI
- decreased body weight / MGI
- male infertility / MGI
- female infertility / MGI
- abnormal gametogenesis / MGI
- abnormal spermiogenesis / MGI
- ovary cysts / MGI
- abnormal gland morphology / MGI
- delayed vaginal opening / MGI
- small uterus / MGI
- small male preputial glands / MGI
- abnormal male preputial gland morphology / MGI
- decreased circulating luteinizing hormone level / MGI
- absent ovarian follicles / MGI
- decreased circulating testosterone level / MGI
- decreased circulating follicle stimulating hormone level / MGI
- no phenotypic analysis / MGI
- absent sexual maturation / MGI
- decreased liver weight / MGI
- abnormal uterus development / MGI
- nervous system phenotype / MGI
- decreased kidney weight / MGI
- abnormal Sertoli cell development / MGI
- decreased testis weight / MGI
- decreased ovary weight / MGI
- decreased uterus weight / MGI
- seminal vesicle hypoplasia / MGI
- azoospermia / MGI
- decreased circulating estradiol level / MGI
- abnormal circulating estradiol level / MGI
- small penis / MGI
- abnormal anogenital distance / MGI
- Leydig cell hypoplasia / MGI
- abnormal spermatid morphology / MGI
- retention of the adrenal gland x-zone / MGI
- anovulation / MGI
- absent estrous cycle / MGI
- abnormal seminal vesicle development / MGI
129-Kiss1tm2(cre/GFP)Coll/H
Status | Available to order |
EMMA ID | EM:11714 |
Citation information | RRID:IMSR_EM:11714 Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information. |
International strain name | 129-Kiss1tm2(cre/GFP)Coll/H |
Alternative name | Kiss1-tm2(cre/GFP)Coll |
Strain type | Targeted Mutant Strains : Knock-in |
Allele/Transgene symbol | Kiss1tm2(cre/GFP)Coll |
Gene/Transgene symbol | Kiss1 |
Information from provider
Provider | William Colledge |
Provider affiliation | PDN, University of Cambridge |
Genetic information | Targeted disruption of Kiss1 gene with insertion of a fused CRE:GFP, the expression of which is driven from the Kiss1 promoter. |
Phenotypic information | Homozygous:Male and female sterilityHeterozygous:No obvious phenotype |
Breeding history | Chimaeras from 129S/SvEv ES cells were crossed with 129 mice from Taconic. |
References | None available |
Homozygous fertile | no |
Homozygous viable | yes |
Homozygous matings required | no |
Immunocompromised | no |
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
- Normosmic congenital hypogonadotropic hypogonadism / Orphanet_432
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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