Human (GRCh37.p13)
Description

solute carrier family 22, member 18 [Source:HGNC Symbol;Acc:10964]

Gene Synonyms

BWR1A, BWSCR1A, HET, IMPT1, ITM, ORCTL2, SLC22A1L, TSSC5, p45-BWR1A

Location

Chromosome 11: 2,920,951-2,946,476 forward strand.

GRCh37:CM000673.1

About this gene

This gene has 13 transcripts (splice variants), 1 paralogue and is associated with 5 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000380574.1SLC22A18-0031755424aaENSP00000369948.1
 
Protein coding
CCDS7740E9PMN7 Q69YM4 Q96BI1
-GENCODE basic
ENST00000312221.5SLC22A18-0011628424aaENSP00000311139.5
 
Protein coding
CCDS7740E9PMN7 Q69YM4 Q96BI1
NM_002555.5GENCODE basic
ENST00000347936.2SLC22A18-0021542424aaENSP00000307859.2
 
Protein coding
CCDS7740E9PMN7 Q69YM4 Q96BI1
NM_183233.2GENCODE basic
ENST00000449793.2SLC22A18-0051225326aaENSP00000392072.2
 
Protein coding
E9PRM7 Q69YM4 -GENCODE basic
ENST00000485423.1SLC22A18-012635134aaENSP00000433019.1
 
Protein coding
E9PMN7 -CDS 3' incomplete
ENST00000441077.1SLC22A18-004831No protein-
 
Processed transcript
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ENST00000498209.2SLC22A18-009782No protein-
 
Processed transcript
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ENST00000492567.2SLC22A18-006684No protein-
 
Processed transcript
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ENST00000449603.1SLC22A18-008682No protein-
 
Processed transcript
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ENST00000467719.1SLC22A18-0132635No protein-
 
Retained intron
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ENST00000463571.1SLC22A18-0071030No protein-
 
Retained intron
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ENST00000495518.1SLC22A18-010588No protein-
 
Retained intron
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ENST00000498244.1SLC22A18-011325No protein-
 
Retained intron
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