- Es15 [Search on AGR]
Mus musculus PHENOTYPE: This locus controls electrophoretic variation in an esterase present in muscle, stomach, heart and testis. The r (rapid) allele is found in M. specilegus; the m (medium) allele in inbred strains; and the l (slow) allele in wild M. musculus from Greece. [provided by MGI curators]
- Esa4 [Search on AGR]
Mus musculus PHENOTYPE: This locus determines polymorphism of an acetyl esterase found in all tissues except hemolysate and serum. The a allele is present in C57BL/10 and other strains; the b allele is present in LP/J, M. m. molossinus, M. m. castaneus and some wild M. musculus. [provided by MGI curators]
- Ldhb [Search on AGR]
Mus musculus PHENOTYPE: Electrophoretic variants of LDHB are determined by: the a allele with fast anodal mobility in all inbred strains tested; and the b allele with slower mobility in Peru-Coppock stock. Three additional variants are known in wild M. spretus from southern France and Spain. Alleles are codominant. [provided by MGI curators]
- Es11 [Search on AGR]
Mus musculus PHENOTYPE: This locus controls polymorphism of a carboxylesterase in liver, kidney and small intestine. The a allele occurs in C57BL, BALB/c and other inbreds; the b allele in IS/Cam and many wild mice; the c allele in M. spretus; the d allele in M. m. molossinus. [provided by MGI curators]
- Es14 [Search on AGR]
Mus musculus PHENOTYPE: This locus controls variation in a butyrylesterase present in erythrocytes and many tissues, but absent from plasma. Laboratory and wild strains of M. musculus carry the r (rapid) allele; M. spretus mice carry the s (slow) allele. [provided by MGI curators]
- mls-2 [Browse genome (BioProject PRJNA13758)] [Search on AGR]
Caenorhabditis elegans Enables RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Involved in several processes, including establishment of mitotic spindle orientation; neuron differentiation involved in amphid sensory organ development; and regulation of cell differentiation. Located in nucleus. Expressed in several structures, including AB lineage cell; AWC-ON; M.dla; head; and somatic nervous system. Human ortholog(s) of this gene implicated in oculoauricular syndrome. Is an ortholog of human HMX1 (H6 family homeobox 1).
- gtl-1 [Browse genome (BioProject PRJNA13758)] [Search on AGR]
Caenorhabditis elegans Predicted to enable monoatomic cation channel activity. Involved in defecation. Predicted to be located in plasma membrane. Human ortholog(s) of this gene implicated in amyotrophic lateral sclerosis-parkinsonism/dementia complex 1; cataract; and congenital stationary night blindness 1C. Is an ortholog of human TRPM1 (transient receptor potential cation channel subfamily M member 1); TRPM3 (transient receptor potential cation channel subfamily M member 3); and TRPM7 (transient receptor potential cation channel subfamily M member 7).
- Ly36 [Search on AGR]
Mus musculus PHENOTYPE: This locus controls an antigen found in thymus, spleen, lymph node, bone marrow, blood, kidney and liver. Of strains tested, Ly36.1 was present only in 4 derived from M. m. molossinus; it was not present in 51 laboratory strains or 11 wild-derived stains. [provided by MGI curators]