- 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
- RN-tre [Search on AGR]
Drosophila melanogaster Related to the N terminus of tre oncogene (RN-tre) encodes a protein involved in border cell migration.
- rn [Search on AGR]
Drosophila melanogaster rotund (rn) encodes a member of the Kruppel zinc-finger transcription factor family. It functions as an olfactory neuron specification factor required for diversification of multiple developmental lineages. rn mutants are defective for multiple distal structures in the adult, including smaller legs, wings and eyes.
- 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]
- nab [Search on AGR]
Drosophila melanogaster nab (nab) encodes a transcriptional co-factor that acts in combination with the transcriptional factors encoded by rn in proximal-distal wing patterning and the product of sqz in CNS development.
- 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]
- Rnf112 [Search on AGR]
Homo sapiens This gene encodes a member of the RING finger protein family of transcription factors. The protein is primarily expressed in brain. The gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]