- Tmgc21 [Search on AGR]
Mus musculus PHENOTYPE: Mutant mice display white belly spotting with white feet. [provided by MGI curators]
- Rgsc58 [Search on AGR]
Mus musculus PHENOTYPE: Mice with a mutation of this gene exhibit white banding, white spotting or scattered white hairs in the dorsal lumbar region. [provided by MGI curators]
- fc [Search on AGR]
Mus musculus PHENOTYPE: Homozygous mice have a white head spot and occassionally a white belly spot. [provided by MGI curators]
- Rgsc1520 [Search on AGR]
Mus musculus PHENOTYPE: Mice with a mutation of this gene exhibit a white belly spot and white tipped digits and tails. [provided by MGI curators]
- eif-2Bgamma [Browse genome (BioProject PRJNA13758)] [Search on AGR]
Caenorhabditis elegans Predicted to enable guanyl-nucleotide exchange factor activity and translation initiation factor activity. Predicted to be involved in cytoplasmic translational initiation. Located in cytoplasm. Human ortholog(s) of this gene implicated in leukoencephalopathy with vanishing white matter 3. Is an ortholog of human EIF2B3 (eukaryotic translation initiation factor 2B subunit gamma).
- prmn-1 [Browse genome (BioProject PRJNA13758)] [Search on AGR]
Caenorhabditis elegans Predicted to be located in membrane. Human ortholog(s) of this gene implicated in cone-rod dystrophy 12; retinal macular dystrophy 2; and retinitis pigmentosa 41. Is an ortholog of human PROM1 (prominin 1) and PROM2 (prominin 2).
- Tmgc19 [Search on AGR]
Mus musculus PHENOTYPE: Mutant mice display pre-weaning lethality in addition to white belly spotting with white patches on nose, face, and body. [provided by MGI curators]
- eif-2Bdelta [Browse genome (BioProject PRJNA13758)] [Search on AGR]
Caenorhabditis elegans Predicted to enable translation initiation factor activity. Involved in several processes, including determination of adult lifespan; lipid storage; and response to stress. Predicted to be located in cytosol. Human ortholog(s) of this gene implicated in leukoencephalopathy with vanishing white matter 4. Is an ortholog of human EIF2B4 (eukaryotic translation initiation factor 2B subunit delta).
- EIF2B5-DT [Search on AGR]
Homo sapiens ASSOCIATED WITH Currarino syndrome; Leukoencephalopathies; leukoencephalopathy with vanishing white matter