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Solute Carrier Family 22, Member 18, Antisense (SLC22A18AS)

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BWSCR1B; ORCTL2S; SLC22A1LS; BWR1B; Organic Cation Transporter-Like Protein 2 Antisense; p27-Beckwith-Wiedemann syndrome chromosomal region 1 candidate gene B

Solute Carrier Family 22, Member 18, Antisense (SLC22A18AS)
CCC P680
HGNC 10965
UniProt Q8N1D0
ORCTL2S gene contains 4 exons spread over approximately 12 kb. It may have multiple transcription start sites or promoters. The ORCTL2 and ORCTL2S genes overlap in their 5-prime regions in divergent orientations, with the first exon of ORCTL2S sharing 31 bp with the second exon of ORCTL2.
The largest open reading frame within the full-length ORCTL2S cDNA encodes a putative 253-amino acid protein. Since ORCTL2S shows no significant similarity to other DNA or protein sequences and lacks good matches to the Kozak and polyadenylation consensus sequences, The ORCTL2S gene may not be translated and may function in the regulation of the ORCTL2 gene. The authors were unable to determine if the ORCTL2S gene is imprinted.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Solute Carrier Family 22, Member 18, Antisense (SLC22A18AS) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Solute Carrier Family 22, Member 18, Antisense (SLC22A18AS) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Solute Carrier Family 22, Member 18, Antisense (SLC22A18AS) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Solute Carrier Family 22, Member 18, Antisense (SLC22A18AS) CLIA Kit Customized Service Offer
n/a ELISA Kit for Solute Carrier Family 22, Member 18, Antisense (SLC22A18AS) ELISA Kit Customized Service Offer
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  2. "Transcriptional map of 170-kb region at chromosome 11p15.5: identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samples."Proc. Natl. Acad. Sci. U.S.A. 95:3873-3878(1998) [PubMed] [Europe PMC] [Abstract]
  3. "Human chromosome 11 DNA sequence and analysis including novel gene identification." Nature 440:497-500(2006) [PubMed] [Europe PMC] [Abstract]
  4. "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
  5. "Paternal imprinting of the SLC22A1LS gene located in the human chromosome segment 11p15.5."BMC Genet. 5:13-13(2004) [PubMed] [Europe PMC] [Abstract]