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 Synb by phenotypic similarity.
Disease | Similarity of phenotypes |
Matching phenotypes | Source |
---|---|---|---|
Silver-Russell Syndrome Due To 11P15 Microduplication | Postnatal growth retardation, Severe intrauterine growth retardation, Short stature, Failure to t... | ORPHA:231144 | |
Intrauterine Growth Retardation With Increased Mitomycin C Sensitivity | Intrauterine growth retardation, Postnatal growth retardation | OMIM:600546 | |
Kagami-Ogata Syndrome Due To Maternal 14Q32.2 Hypermethylation | Postnatal growth retardation, Large for gestational age, Large placenta, Umbilical hernia, Small ... | ORPHA:254534 |
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MGI Allele | Allele Type | Produced |
---|---|---|
Synbtm97248(L1L2_Bact_P) | KO first allele (reporter-tagged insertion with conditional potential) | Targeting vectors |
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