Gene: Zfp687 MGI:1925516
Log in to followHuman diseases caused by Zfp687 mutations
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 Zfp687 by orthology or direct annotation.
Disease | Similarity of phenotypes |
Matching phenotypes | Source |
---|---|---|---|
Paget Disease Of Bone 6 | OMIM:616833 |
The table below shows human diseases predicted to be associated to Zfp687 by phenotypic similarity.
Disease | Similarity of phenotypes |
Matching phenotypes | Source |
---|---|---|---|
Paget Disease Of Bone 6 | OMIM:616833 |
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MGI Allele | Allele Type | Produced |
---|---|---|
Zfp687tm1(KOMP)Vlcg | Reporter-tagged deletion allele (with selection cassette) | ES Cells |
Zfp687tm1(KOMP)Wtsi | Reporter-tagged deletion allele (with selection cassette) | Targeting vectors, ES Cells |
Zfp687tm463624(Ifitm2_intron_L1L2_GT1_LF2A_LacZ_BetactP_neo) | KO first allele (reporter-tagged insertion with conditional potential) | Targeting vectors |
Zfp687em1(IMPC)Bay | Inter-exon deletion | Mice |
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