The SLC22A18 gene homepage

General information
Gene symbol SLC22A18
Gene name solute carrier family 22, member 18
Chromosome 11
Chromosomal band p15.5
Imprinted Unknown
Genomic reference NG_011512.1
Transcript reference NM_183233.2
Associated with diseases cancer, breast, cancer, lung, RMSE1
Citation reference(s) -
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 92
Unique public DNA variants reported 82
Individuals with public variants 0
Hidden variants 31
Date created May 03, 2013
Date last updated May 09, 2022
Version SLC22A18:220509

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 10964
Entrez Gene 5002
PubMed articles SLC22A18
OMIM - Gene 602631
OMIM - Diseases cancer, breast (cancer, breast, susceptibility)
cancer, lung (cancer, lung (adenocarcinoma))
RMSE1 (rhabdomyosarcoma, embryonal, type 1 (RMSE-1))
Orphanet SLC22A18


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00019168 11 transcript variant 2 NM_183233.2 NP_899056.2 92


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