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 Cog1 by orthology or direct annotation.
| Disease | Similarity of phenotypes |
Matching phenotypes | Source |
|---|---|---|---|
| Cog1-Cdg | ORPHA:263508 | ||
| Congenital Disorder Of Glycosylation, Type Iig | OMIM:611209 |
The table below shows human diseases predicted to be associated to Cog1 by phenotypic similarity.
| Disease | Similarity of phenotypes |
Matching phenotypes | Source |
|---|---|---|---|
| Cog1-Cdg | ORPHA:263508 | ||
| Congenital Disorder Of Glycosylation, Type Iig | OMIM:611209 |
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| MGI Allele | Allele Type | Produced |
|---|---|---|
| Cog1tm1e(EUCOMM)Wtsi | Targeted, non-conditional allele | ES Cells |
| Cog1tm1a(EUCOMM)Hmgu | KO first allele (reporter-tagged insertion with conditional potential) | Targeting vectors, ES Cells |
| Cog1tm47402(L1L2_gt0) | KO first allele (reporter-tagged insertion with conditional potential) | Targeting vectors |
| Cog1em1(IMPC)Bay | Exon Deletion | Mice |
| Cog1tm1a(EUCOMM)Wtsi | KO first allele (reporter-tagged insertion with conditional potential) | Targeting vectors, ES Cells |
| Cog1tm1e(EUCOMM)Hmgu | Targeted, non-conditional allele | ES Cells |
| Cog1tm2a(EUCOMM)Wtsi | KO first allele (reporter-tagged insertion with conditional potential) | Targeting vectors, ES Cells |
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