- abnormal xiphoid process morphology / MGI
- abnormal hair follicle morphology / MGI
- short snout / MGI
- abnormal spermatogenesis / MGI
- thin skin / MGI
- male infertility / MGI
- emphysema / MGI
- no abnormal phenotype detected / MGI
- oligozoospermia / MGI
- abnormal molar morphology / MGI
- abnormal cutaneous collagen fibril morphology / MGI
- triangular face / MGI
B6;129P2-Adamts2tm1Dgen/H
Status | Available to order |
EMMA ID | EM:02292 |
Citation information | RRID:IMSR_EM:02292 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 | B6;129P2-Adamts2tm1Dgen/H |
Alternative name | DELTAGEN_T1229 |
Strain type | Targeted Mutant Strains : Knock-out |
Allele/Transgene symbol | Adamts2tm1Dgen |
Gene/Transgene symbol | Adamts2 |
Information from provider
Provider | Deltagen Inc. |
Provider affiliation | Deltagen Inc. |
Phenotypic information | There were no significant differences detected in the homozygous mutant mice when compared with age- and gender-matched wild-type control mice. |
References | None available |
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
- Dermatosparaxis Ehlers-Danlos syndrome / Orphanet_1901
MGI phenotypes (gene matching)
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