- rab-33 [Browse genome (BioProject PRJNA13758)] [Search on AGR]
Caenorhabditis elegans Predicted to enable GTP binding activity and GTPase activity. Predicted to be involved in autophagosome assembly. Predicted to be located in Golgi apparatus and endosome. Human ortholog(s) of this gene implicated in Smith-McCort dysplasia 2. Is an ortholog of human RAB33B (RAB33B, member RAS oncogene family).
- MTOR-AS1 [Search on AGR]
Homo sapiens ASSOCIATED WITH genetic disease; Smith-Kingsmore Syndrome; INTERACTS WITH 2-hydroxypropanoic acid; rac-lactic acid
- Sdr2 [Search on AGR]
Mus musculus PHENOTYPE: This locus controls level of liver serine dehydratase, but not of phosphoenolpyruvate carboxykinase, induced by a 48-hour fast. BALB/cJ carries the a allele for high induction level; AKR and most inbreds carry the b allele for low induction level. (BALB/cJ x AKR)F1 hybrids are intermediate. [provided by MGI curators]
- Slc47a1 [Search on AGR]
Homo sapiens This gene is located within the Smith-Magenis syndrome region on chromosome 17. It encodes a protein of unknown function. [provided by RefSeq, Jul 2008]
- Tol1 [Search on AGR]
Mus musculus PHENOTYPE: This locus controls susceptibility to induction of tolerance to bovine gamma-globulin (BCG). The dominant a allele determines susceptibility to induction of tolerance in DBA/2J; the b allele determines resistance in BALB/cJ. [provided by MGI curators]
- Es29 [Search on AGR]
Mus musculus PHENOTYPE: Activity variants for this testosterone-dependent structural esterase locus are detected by disc electrophoresis. Alleles are: SEG/1, null; BALB/cJ and most inbreds, strong activity; MOLH/Fre, weak activity. Expression also is partly controlled by a second locus, Mse1. [provided by MGI curators]
- Cotl1 [Search on AGR]
Homo sapiens This gene encodes one of the numerous actin-binding proteins which regulate the actin cytoskeleton. This protein binds F-actin, and also interacts with 5-lipoxygenase, which is the first committed enzyme in leukotriene biosynthesis. Although this gene has been reported to map to chromosome 17 in the Smith-Magenis syndrome region, the best alignments for this gene are to chromosome 16. The Smith-Magenis syndrome region is the site of two related pseudogenes. [provided by RefSeq, Jul 2008]
- H2-Q3 [Search on AGR]
Mus musculus PHENOTYPE: This locus controls a serologically detected antigen limited predominantly Thy1+ cells of lymph node and spleen. The a allele determines presence of antigen in BALB/cJ, C56BL/6, and A; the b allele determines absence of antigen in DBA/1 and SWR. [provided by MGI curators]