Not currently registered for phenotyping at IMPC
Phenotyping is currently not planned for a knockout strain of this gene.
Gene Summary
IMPC Data Collections
- No Body Weight Data
- No Embryo Imaging Data
- No Viability Data
Phenotyping is currently not planned for a knockout strain of this gene.
The analysis uses data from IMPC, along with published data on other mouse mutants, in comparison to human disease reports in OMIM, Orphanet, and DECIPHER.
Phenotype comparisons summarize the similarity of mouse phenotypes with human disease phenotypes.
The table below shows human diseases associated to Nup107 by orthology or direct annotation.
Disease | Similarity of phenotypes |
Matching phenotypes | Source |
---|---|---|---|
46,Xx Gonadal Dysgenesis | Secondary amenorrhea, Streak ovary, Primary amenorrhea, Premature ovarian insufficiency, Decrease... | ORPHA:243 | |
Nephrotic Syndrome, Type 11 | OMIM:616730 | ||
Galloway-Mowat Syndrome | ORPHA:2065 | ||
Galloway-Mowat Syndrome 7 | OMIM:618348 | ||
Ovarian Dysgenesis 6 | OMIM:618078 | ||
Genetic Steroid-Resistant Nephrotic Syndrome | ORPHA:656 |
The table below shows human diseases predicted to be associated to Nup107 by phenotypic similarity.
Disease | Similarity of phenotypes |
Matching phenotypes | Source |
---|---|---|---|
Spermatogenic Failure 3 | Infertility | OMIM:606766 | |
Oocyte Maturation Defect 4 | Infertility | OMIM:617743 | |
Spermatogenic Failure 27 | Infertility | OMIM:617965 | |
Oocyte Maturation Defect 1 | Infertility | OMIM:615774 | |
Oocyte Maturation Defect 5 | Infertility | OMIM:617996 | |
Spermatogenic Failure 17 | Infertility | OMIM:617214 | |
Oocyte Maturation Defect 3 | Infertility | OMIM:617712 | |
Oocyte Maturation Defect 2 | Female infertility, Oocyte arrest at metaphase I | OMIM:616780 | |
Female Infertility Due To Oocyte Meiotic Arrest | Female infertility, Abnormal meiosis, Oocyte arrest at metaphase I | ORPHA:488191 | |
Premature Ovarian Failure 15 | Oligomenorrhea | OMIM:618096 | |
Premature Ovarian Failure 13 | Oligomenorrhea | OMIM:617442 | |
Progesterone Resistance | Female infertility | OMIM:264080 | |
Oocyte Maturation Defect 6 | Female infertility | OMIM:618353 | |
Oocyte Maturation Defect 11 | Female infertility | OMIM:619643 | |
Oocyte Maturation Defect 7 | Female infertility | OMIM:618550 | |
Preimplantation Embryonic Lethality 1 | Female infertility | OMIM:616814 | |
Premature Ovarian Failure 19 | Secondary amenorrhea, Female infertility, Irregular menstruation, Premature ovarian insufficiency | OMIM:619245 | |
Ovarian Dysgenesis 3 | Primary amenorrhea | OMIM:614324 | |
Pregnancy Loss, Recurrent, Susceptibility To, 3 | Recurrent spontaneous abortion | OMIM:614391 | |
Pregnancy Loss, Recurrent, Susceptibility To, 2 | Recurrent spontaneous abortion | OMIM:614390 | |
Pregnancy Loss, Recurrent, Susceptibility To, 1 | Recurrent spontaneous abortion | OMIM:614389 | |
46,Xx Gonadal Dysgenesis | Secondary amenorrhea, Streak ovary, Primary amenorrhea, Premature ovarian insufficiency, Decrease... | ORPHA:243 | |
Ovarian Dysgenesis 6 | OMIM:618078 | ||
Nephrotic Syndrome, Type 11 | OMIM:616730 | ||
Galloway-Mowat Syndrome | ORPHA:2065 | ||
Genetic Steroid-Resistant Nephrotic Syndrome | ORPHA:656 | ||
Galloway-Mowat Syndrome 7 | OMIM:618348 |
All available products are supplied via our member's centres or partnerships. When ordering a product from the IMPC you will be redirected to one of their websites or prompted to start an email.
This service may be affected by the Covid-19 pandemic. See how
MGI Allele | Allele Type | Produced |
---|---|---|
Nup107tm372119(L1L2_Bact_P) | KO first allele (reporter-tagged insertion with conditional potential) | Targeting vectors |
Get highlights of the most important data releases, news and events, delivered straight to your email inbox
Subscribe to newsletter