SLC22A18AS
SNPs given by the user that are near or inside this gene:
| SNP |
Distance (bp) |
Direction |
|---|
| rs2237892 |
69576 |
downstream |
| rs231362 |
217856 |
downstream |
| OMIM ID: | `OMIM ID 603240
`_ |
|---|
No phenotypes found linked to this gene.
- molecular_function
- cellular_component
- biological_process
No pathways found linked to this gene.
- Results suggest imprinting of the paternal allele of SLC22A1LS gene in five fetal tissues: brain, liver, placenta, kidneys and lungs. [PMID 15175115]
- SLC22A18/SLC22A18AS genes are a sense-antisense pair located at human chromosome segment 11p15.5. These genes are paternally imprinted. [PMID 18721868]
- Using antibodies generated in rabbit, immunoprecipitation and Western blot analyses, translation of a 253-aa ORF at very low levels occurred. The translated protein was mainly localized in the cytoplasm. [PMID 18721868]
Recent articles:
- Bajaj V et al. “Promoter characterization and regulation of expression of an imprinted gene SLC22A18AS.” Gene. 2008 Nov 15;424(1-2):40-7. PMID 18721868
- Gerhard DS et al. “The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).” Genome Res. 2004 Oct;14(10B):2121-7. PMID 15489334
- Bajaj V et al. “Paternal imprinting of the SLC22A1LS gene located in the human chromosome segment 11p15.5.” BMC Genet. 2004 Jun 3;5:13. PMID 15175115
- Strausberg RL et al. “Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.” Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16899-903. PMID 12477932
- Cooper PR et al. “Divergently transcribed overlapping genes expressed in liver and kidney and located in the 11p15.5 imprinted domain.” Genomics. 1998 Apr 1;49(1):38-51. PMID 9570947
- Schwienbacher C et al. “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. 1998 Mar 31;95(7):3873-8. PMID 9520460