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 predicted to be associated to Vmn2r1 by phenotypic similarity.
Disease | Similarity of phenotypes |
Matching phenotypes | Source |
---|---|---|---|
Holoprosencephaly 4 | Depressed nasal bridge, Depressed nasal tip, Absent nasal septal cartilage | OMIM:142946 | |
Isolated Arrhinia | Underdeveloped nasal alae, Midline defect of the nose, Aplasia/Hypoplasia of the nasal septum, Hy... | ORPHA:1134 | |
Cleft Lip/Palate-Deafness-Sacral Lipoma Syndrome | Depressed nasal ridge, Absent nasal septal cartilage | ORPHA:2003 |
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MGI Allele | Allele Type | Produced |
---|---|---|
Vmn2r1tm88458(L1L2_Bact_P) | KO first allele (reporter-tagged insertion with conditional potential) | Targeting vectors |
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