- Pcf11 [Search on AGR]
Homo sapiens The protein encoded by this gene binds to CLP1 to form pre-mRNA cleavage factor IIm. The encoded protein is necessary for efficient Pol II transcription termination and may be involved in degradation of the 3' product of polyA site cleavage. [provided by RefSeq, Oct 2016]
- Rps27a-ps29 [Search on AGR]
Rattus norvegicus This locus was determined to be a processed pseudogene of Rps27a (GeneID:100912032) since it has a similar nucleotide sequence to the coding region of the parental gene, but the coding region is disrupted by indels. This locus contains only the exonic sequence relative to the parental gene and has a polyA-rich region in the genome at the 3' end. [provided by RefSeq, May 2015]
- Rps27a-ps15 [Search on AGR]
Rattus norvegicus This locus was determined to be a processed pseudogene of Rps27a (GeneID: 100912032) since it has a similar nucleotide sequence to the coding region of the parental gene, but contains no intact open reading frame. Consistent with this locus being a processed pseudogene, it contains only exonic sequences relative to the parental gene, and has a polyA region in the genome at the 3' end of the gene. [provided by RefSeq, Apr 2015]
- Rps27a-ps21 [Search on AGR]
Rattus norvegicus This locus was determined to be a processed pseudogene of Rps27a (GeneID: 100912032) since it has a similar nucleotide sequence to the coding region of the parental gene, but contains no intact open reading frame. Consistent with this locus being a processed pseudogene, it contains only exonic sequences relative to the parental gene and has a polyA-rich region in the genome at the 3' end of the gene. [provided by RefSeq, Apr 2015]
- Scel [Search on AGR]
Homo sapiens The protein encoded by this gene is a precursor to the cornified envelope of terminally differentiated keratinocytes. This protein localizes to the periphery of cells and may function in the assembly or regulation of proteins in the cornified envelope. Transcript variants encoding different isoforms exist. A transcript variant utilizing an alternative polyA signal has been described in the literature, but its full-length nature has not been determined. [provided by RefSeq, Jul 2008]
- Rps27a-ps23 [Search on AGR]
Rattus norvegicus This locus was determined to be a processed pseudogene of Rps27a (GeneID: 100912032) since it has a similar nucleotide sequence to the coding region of the parental gene, but contains no intact open reading frame. Consistent with this locus being a processed pseudogene, it contains only exonic sequences relative to the parental gene and has a polyA-rich region in the genome at the 3' end of the gene. [provided by RefSeq, Apr 2015]
- Rps27a-ps8 [Search on AGR]
Rattus norvegicus This locus was determined to be a processed pseudogene of Rps27a (GeneID:100912032) since it has a similar nucleotide sequence to the coding region of the parental gene, but contains no intact open reading frame. Consistent with this locus being a processed pseudogene, it contains only exonic sequences relative to the parental gene, and has a polyA region in the genome at the 3' end of the gene. [provided by RefSeq, Apr 2015]
- TMEM183BP [Search on AGR]
Homo sapiens This locus was thought to represent a pseudogene of chromosome 1 open reading frame 37 because it is intronless and retains a polyA tail at the 3' end. It does however contain a complete open reading frame that subsequent research has demonstrated to be transcribed in a limited number of human tissues. The encoded protein may represent a transmembrane protein associated with cell membranes and be involved in cell-cell or cell-environment interactions. [provided by RefSeq, Jul 2010]
- Pabpc5 [Search on AGR]
Homo sapiens This gene encodes a protein that binds to the polyA tail found at the 3' end of most eukaryotic mRNAs. It is thought to play a role in the regulation of mRNA metabolic processes in the cytoplasm. This gene is located in a gene-poor region within the X-specific 13d-sY43 subinterval of the chromosome Xq21.3/Yp11.2 homology block. It is located close to translocation breakpoints associated with premature ovarian failure, and is therefore a potential candidate gene for this disorder. [provided by RefSeq, May 2010]
- Ssr1 [Search on AGR]
Homo sapiens The signal sequence receptor (SSR) is a glycosylated endoplasmic reticulum (ER) membrane receptor associated with protein translocation across the ER membrane. The SSR consists of 2 subunits, a 34-kD glycoprotein encoded by this gene and a 22-kD glycoprotein. This gene generates several mRNA species as a result of complex alternative polyadenylation. This gene is unusual in that it utilizes arrays of polyA signal sequences that are mostly non-canonical. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014]