| 733606 | CCS | copper chaperone for superoxide dismutase | Copper chaperone for superoxide dismutase specifically delivers Cu to copper/zinc superoxide dismutase and may activate copper/zinc superoxide dismutase through direct insertion of the Cu cofactor. [provided by RefSeq, Jul 2008] | 11 | 66593185 | 66606019 | Human | 184 | symbol , COSMIC , Human Proteome Map | gene, protein-coding, REVIEWED [RefSeq] |
| 68966 | EEF1A1 | eukaryotic translation elongation factor 1 alpha 1 | This gene encodes an isoform of the alpha subunit of the elongation factor-1 complex, which is responsible for the enzymatic delivery of aminoacyl tRNAs to the ribosome. This isoform (alpha 1) is expressed in brain, placenta, lung, liver, kidney, and pancreas, and the other isoform (alpha 2) is expr essed in brain, heart and skeletal muscle. This isoform is identified as an autoantigen in 66% of patients with Felty syndrome. This gene has been found to have multiple copies on many chromosomes, some of which, if not all, represent different pseudogenes. [provided by RefSeq, Jul 2008] | 6 | 73515750 | 73521032 | Human | 309 | old_gene_symbol | gene, protein-coding, REVIEWED [RefSeq] |
| 1602440 | CCSAP | centriole, cilia and spindle associated protein | Enables microtubule binding activity. Involved in mitotic spindle microtubule depolymerization and regulation of mitotic spindle assembly. Located in axon; ciliary transition zone; and cytoskeleton. [provided by Alliance of Genome Resources, Jul 2025] | 1 | 229321015 | 229343047 | Human | 91 | symbol , COSMIC , Human Proteome Map | gene, protein-coding, VALIDATED [RefSeq] |
| 1602258 | CCSER1 | coiled-coil serine rich protein 1 | Implicated in cocaine dependence. [provided by Alliance of Genome Resources, Apr 2025] | 4 | 90127394 | 91605295 | Human | 61 | symbol , COSMIC , Human Proteome Map | gene, protein-coding, VALIDATED [RefSeq] |
| 1312172 | CCSER2 | coiled-coil serine rich protein 2 | Predicted to enable microtubule binding activity. Predicted to be involved in microtubule bundle formation. Predicted to be located in cytoplasm and cytoskeleton. Predicted to be active in microtubule cytoskeleton. [provided by Alliance of Genome Resources, Jul 2025] | 10 | 84328589 | 84518517 | Human | 79 | symbol , COSMIC , Human Proteome Map | gene, protein-coding, VALIDATED [RefSeq] |
| 38638626 | CCSER2P1 | CCSER2 pseudogene 1 | | 9 | 102515164 | 102516842 | Human | | symbol , GTEx , COSMIC , name , Human Proteome Map | gene, pseudo, INFERRED [RefSeq] |
| 151669119 | CCSER1-AS1 | CCSER1 antisense RNA 1 | | 4 | 91268585 | 91325201 | Human | | symbol , GTEx , COSMIC , name , Human Proteome Map | gene, ncrna, MODEL [RefSeq] |
| 735247 | SCGB1A1 | secretoglobin family 1A member 1 | This gene encodes a member of the secretoglobin family of small secreted proteins. The encoded protein has been implicated in numerous functions including anti-inflammation, inhibition of phospholipase A2 and the sequestering of hydrophobic ligands. Defects in this gene are associated with a suscept ibility to asthma. [provided by RefSeq, May 2010] | 11 | 62419033 | 62423195 | Human | 184 | old_gene_symbol | gene, protein-coding, REVIEWED [RefSeq] |
| 2302834 | BHLHA9 | basic helix-loop-helix family member a9 | This gene is a member of the basic helix-loop-helix family. The encoded protein is a transcription factor involved in limb development. Mutations in this gene have been associated with mesoaxial synostotic syndactyly Malik-Percin type (MSSD). Copy number variation of a locus containing this gene has been linked to a form of split-hand/foot malformation with long bone deficiency (SHFLD3). [provided by RefSeq, Mar 2015] | 17 | 1270444 | 1271815 | Human | 137 | old_gene_symbol | gene, protein-coding, REVIEWED [RefSeq] |
| 1313176 | CEMIP | cell migration inducing hyaluronidase 1 | Enables several functions, including clathrin heavy chain binding activity; hyaluronic acid binding activity; and hyalurononglucosaminidase activity. Involved in several processes, including hyaluronan catabolic process; positive regulation of protein phosphorylation; and positive regulation of prot ein targeting to membrane. Located in several cellular components, including clathrin-coated endocytic vesicle; endoplasmic reticulum; and nucleus. [provided by Alliance of Genome Resources, Jul 2025] | 15 | 80779370 | 80951771 | Human | 163 | old_gene_symbol | gene, protein-coding, VALIDATED [RefSeq] |
| 1603244 | VWA2 | von Willebrand factor A domain containing 2 | This gene encodes a member of the von Willebrand factor A-like domain protein superfamily. The encoded protein is localized to the extracellular matrix and may serve as a structural component in basement membranes or in anchoring structures on scaffolds of collagen VII or fibrillin. This gene has be en linked to type 1A diabetes and is a candidate serological marker for colon cancer. [provided by RefSeq, Jan 2013] | 10 | 114239254 | 114294500 | Human | 47 | old_gene_symbol | gene, protein-coding, REVIEWED [RefSeq] |
| 1605551 | UQCC4 | ubiquinol-cytochrome c reductase complex assembly factor 4 | Predicted to be involved in mitochondrial respiratory chain complex III assembly. Located in mitochondrion. [provided by Alliance of Genome Resources, Jul 2025] | 16 | 1419752 | 1420747 | Human | 35 | old_gene_symbol | gene, protein-coding, VALIDATED [RefSeq] |
| 16558368 | AC074124.1 | novel transcript, antisense to CCSER1 | | | | | Human | | name | gene, lncrna |
