- LINC02714 [Search on AGR]
Homo sapiens ASSOCIATED WITH amenorrhea; Chromosome 11, Partial Trisomy 11q; Jacobsen Syndrome
- LINC02873 [Search on AGR]
Homo sapiens ASSOCIATED WITH Chromosome 11, Partial Trisomy 11q; Dwarfism; Jacobsen Syndrome; INTERACTS WITH titanium dioxide
- LINC02743 [Search on AGR]
Homo sapiens ASSOCIATED WITH Chromosome 11, Partial Trisomy 11q; Jacobsen Syndrome; Schizophrenia; INTERACTS WITH permethrin
- T10B10.4 [Browse genome (BioProject PRJNA13758)] [Search on AGR]
Caenorhabditis elegans Predicted to enable N-acyltransferase activity. Located in endoplasmic reticulum. Is an ortholog of several human genes including GLYAT (glycine-N-acyltransferase); GLYATL1 (glycine-N-acyltransferase like 1); and GLYATL2 (glycine-N-acyltransferase like 2).
- F43H9.4 [Browse genome (BioProject PRJNA13758)] [Search on AGR]
Caenorhabditis elegans Predicted to enable N-acyltransferase activity. Predicted to be located in mitochondrion. Is an ortholog of several human genes including GLYAT (glycine-N-acyltransferase); GLYATL1 (glycine-N-acyltransferase like 1); and GLYATL2 (glycine-N-acyltransferase like 2).
- hst-1 [Browse genome (BioProject PRJNA13758)] [Search on AGR]
Caenorhabditis elegans Predicted to enable [heparan sulfate]-glucosamine N-sulfotransferase activity and deacetylase activity. Predicted to be involved in heparan sulfate proteoglycan biosynthetic process, polysaccharide chain biosynthetic process. Predicted to be located in Golgi apparatus. Human ortholog(s) of this gene implicated in autosomal recessive intellectual developmental disorder 46. Is an ortholog of several human genes including NDST1 (N-deacetylase and N-sulfotransferase 1); NDST2 (N-deacetylase and N-sulfotransferase 2); and NDST3 (N-deacetylase and N-sulfotransferase 3).