- Def6 [Search on AGR]
Homo sapiens DEF6, or IBP, is a guanine nucleotide exchange factor (GEF) for RAC (MIM 602048) and CDC42 (MIM 116952) that is highly expressed in B and T cells (Gupta et al., 2003 [PubMed 12923183]).[supplied by OMIM, Mar 2008]
- Cutc [Search on AGR]
Homo sapiens Members of the CUT family of copper transporters are associated with copper homeostasis and are involved in the uptake, storage, delivery, and efflux of copper (Gupta et al., 1995 [PubMed 7635807]; Li et al., 2005 [PubMed 16182249]).[supplied by OMIM, Mar 2008]
- Rgsc665 [Search on AGR]
Mus musculus PHENOTYPE: Mice with a mutation of this gene have elevated blood pressure vs. that of controls. [provided by MGI curators]
- Rgsc709 [Search on AGR]
Mus musculus PHENOTYPE: Mice with a mutation of this gene have reduced blood pressure vs. that of control mice. [provided by MGI curators]
- Rgsc676 [Search on AGR]
Mus musculus PHENOTYPE: Mice with a mutation of this gene have reduced blood pressure vs. that of control mice. [provided by MGI curators]
- Scarf2 [Search on AGR]
Rattus norvegicus Predicted to enable scavenger receptor activity. Predicted to be involved in heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules. Human ortholog(s) of this gene implicated in Van den Ende-Gupta syndrome. Orthologous to human SCARF2 (scavenger receptor class F member 2); INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine; 6-propyl-2-thiouracil; acetamide.
- prp-17 [Browse genome (BioProject PRJNA13758)] [Search on AGR]
Caenorhabditis elegans Predicted to enable mRNA binding activity. Predicted to be involved in mRNA splicing, via spliceosome. Predicted to be part of catalytic step 2 spliceosome. Human ortholog(s) of this gene implicated in pontocerebellar hypoplasia type 15. Is an ortholog of human CDC40 (cell division cycle 40).
- RBH2 [Search on AGR]
Saccharomyces cerevisiae Putative protein of unknown function; expression repressed in carbon limited vs carbon replete chemostat cultures; non-essential gene; contains a PH-like domain; RBH2 has a paralog, RBH1, that arose from the whole genome duplication