Description

solute carrier family 22 member 1 [Source:HGNC Symbol;Acc:HGNC:10963]

Synonyms

OCT1

Location

Chromosome 6: 160,121,789-160,158,718 forward strand.

GRCh38:CM000668.2

About this gene

This gene has 7 transcripts (splice variants), 92 orthologues, 16 paralogues, is a member of 1 Ensembl protein family and is associated with 22 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
SLC22A1-202ENST00000366963.81948554aaENSP00000355930
 
Protein coding
CCDS5274O15245 NM_003057
NM_153187
NP_003048
NP_694857
TSL:1GENCODE basicAPPRIS P1
SLC22A1-201ENST00000324965.81521506aaENSP00000318103
 
Protein coding
CCDS5275O15245 -TSL:5GENCODE basic
SLC22A1-203ENST00000457470.61452483aaENSP00000409557
 
Protein coding
-O15245 -TSL:5GENCODE basic
SLC22A1-207ENST00000540443.165348aaENSP00000440105
 
Protein coding
-F5GY86 -CDS 3' incompleteTSL:3
SLC22A1-206ENST00000539263.51598140aaENSP00000443245
 
Nonsense mediated decay
-F5H5P3 -TSL:5
SLC22A1-204ENST00000460902.21484353aaENSP00000439274
 
Nonsense mediated decay
-O15245 -TSL:5
SLC22A1-205ENST00000478607.1324No protein-
 
Retained intron
---TSL:2

Gene-based displays