Vstm2l | V-set and transmembrane domain containing 2-like
Physiological systems
17 / 24 physiological systems tested
2 Significantly impacted by the knock-out
Vision/eye Cardiovascular system
15 No significant impact
7 Not tested
Data collections
Gene metrics:2Significant phenotypes
0Associated diseases
Expression examined in:0Adult tissues
0Embryo tissues
abnormal retina vasculature morphology | 1 supporting dataset | Vstm2lem1(IMPC)Tcp | homozygote | Early adult | 3.59x10-7 | ||
abnormal retina blood vessel morphology | 1 supporting dataset | Vstm2lem1(IMPC)Tcp | homozygote | Early adult | 3.03x10-7 |
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Human diseases caused by Vstm2l 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.
External links
No external links available for Vstm2l.
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Vstm2lem1(IMPC)Tcp | Exon Deletion | | mouse |
Vstm2ltm102476(L1L2_Bact_P) | KO first allele (reporter-tagged insertion with conditional potential) | | targeting vector |