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Human (GRCh38.p14)
Description

solute carrier family 52 member 1 [Source:HGNC Symbol;Acc:HGNC:30225]

Gene Synonyms

FLJ10060, GPCR42, GPR172B, HRFT1, PAR2, RFVT1

Location

Chromosome 17: 5,032,600-5,052,009 reverse strand.

GRCh38:CM000679.2

About this gene

This gene has 10 transcripts (splice variants), 172 orthologues, 2 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000254853.10SLC52A1-2012375448aaENSP00000254853.5
 
Protein coding
CCDS11066Q9NWF4-1 NM_017986.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000512825.7SLC52A1-2032992350aaENSP00000443026.1
 
Protein coding
F5H5Y1 -GENCODE PrimaryGENCODE BasicTSL:2
ENST00000923984.1SLC52A1-2072461448aaENSP00000594043.1
 
Protein coding
CCDS11066--GENCODE PrimaryGENCODE BasicAPPRIS P1
ENST00000424747.1SLC52A1-2022412448aaENSP00000399979.1
 
Protein coding
CCDS11066Q9NWF4-1 -GENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000961591.1SLC52A1-2102362448aaENSP00000631650.1
 
Protein coding
CCDS11066--GENCODE PrimaryGENCODE BasicAPPRIS P1
ENST00000961589.1SLC52A1-2082071448aaENSP00000631648.1
 
Protein coding
CCDS11066--GENCODE BasicAPPRIS P1
ENST00000961590.1SLC52A1-2092011448aaENSP00000631649.1
 
Protein coding
CCDS11066--GENCODE BasicAPPRIS P1
ENST00000894338.1SLC52A1-2061900448aaENSP00000564397.1
 
Protein coding
CCDS11066--GENCODE BasicAPPRIS P1
ENST00000573674.1SLC52A1-2042490No protein-
 
Retained intron
--TSL:2
ENST00000575919.1SLC52A1-2052385No protein-
 
Retained intron
--TSL:5