D630023F18Rik | RIKEN cDNA D630023F18 gene
GeneMGI:2138198
Physiological systems
18 / 24 physiological systems tested
2 Significantly impacted by the knock-out
Vision/eye Mortality/aging
16 No significant impact
6 Not tested
Data collections
Gene metrics:2Significant phenotypes
0Associated diseases
Expression examined in:45Adult tissues
0Embryo tissues
abnormal retina morphology | 1 supporting dataset | D630023F18Riktm1b(KOMP)Wtsi | homozygote | Early adult | 9.25x10-6 | ||
preweaning lethality, incomplete penetrance | 1 supporting dataset | D630023F18Riktm1b(KOMP)Wtsi | homozygote | Early adult | N/A * |
| | | | | | | | | |
adrenal gland | heterozygote | n/a | 0% (0/2) | 0.7% (4/570) |
aorta | heterozygote | n/a | 0% (0/2) | 0.19% (1/533) |
blood vessel | heterozygote | n/a | 0% (0/2) | 0% (0/173) |
bone | heterozygote | n/a | 0% (0/2) | 0% (0/394) |
brain | heterozygote | n/a | 0% (0/2) | 0.86% (5/579) |
brainstem | heterozygote | n/a | 0% (0/2) | 0.41% (2/490) |
brown adipose tissue | heterozygote | n/a | 0% (0/2) | 0% (0/588) |
cartilage tissue | heterozygote | n/a | 0% (0/2) | 0.22% (1/454) |
cerebellum | heterozygote | n/a | 0% (0/2) | 0.56% (3/532) |
cerebral cortex | heterozygote | n/a | 0% (0/2) | 0.41% (2/491) |
Human diseases caused by D630023F18Rik 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 D630023F18Rik.
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D630023F18Riktm1a(KOMP)Wtsi | KO first allele (reporter-tagged insertion with conditional potential) | | targeting vector ES Cell mouse |
D630023F18Riktm1b(KOMP)Wtsi | Reporter-tagged deletion allele (with selection cassette) | | mouse |
D630023F18Riktm1e(KOMP)Wtsi | Targeted, non-conditional allele | | ES Cell |
D630023F18Riktm45017(L1L2_gt0) | KO first allele (reporter-tagged insertion with conditional potential) | | targeting vector |