Human (GRCh38.p14)
Description

solute carrier family 52 member 3 [Source:HGNC Symbol;Acc:HGNC:16187]

Gene Synonyms

BA371L19.1, C20ORF54, HRFT2, RFT2, RFVT3

Location

Chromosome 20: 760,080-776,015 reverse strand.

GRCh38:CM000682.2

About this gene

This gene has 9 transcripts (splice variants), 210 orthologues, 2 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000645534.1SLC52A3-2052611469aaENSP00000494193.1
 
Protein coding
CCDS13007Q9NQ40-1 NM_033409.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1
ENST00000381944.5SLC52A3-2023206415aaENSP00000371370.3
 
Protein coding
Q9NQ40-2 -GENCODE basicTSL:2
ENST00000488495.3SLC52A3-2043106469aaENSP00000494009.1
 
Protein coding
CCDS13007Q9NQ40-1 -GENCODE basicAPPRIS P1TSL:3
ENST00000675066.1SLC52A3-2072674364aaENSP00000501902.1
 
Protein coding
A0A6Q8PFQ2 -GENCODE basic
ENST00000217254.11SLC52A3-2012654469aaENSP00000217254.7
 
Protein coding
CCDS13007Q9NQ40-1 -GENCODE basicAPPRIS P1TSL:5
ENST00000473664.2SLC52A3-2031901336aaENSP00000502741.1
 
Protein coding
A0A6Q8PHL7 -GENCODE basicTSL:5
ENST00000674666.1SLC52A3-20691144aaENSP00000502783.1
 
Protein coding
A0A6Q8PHL2 -CDS 3' incomplete
ENST00000676154.1SLC52A3-209766228aaENSP00000501807.1
 
Protein coding
A0A6Q8PFG7 -CDS 3' incomplete
ENST00000675466.1SLC52A3-2081001No protein-
 
Protein coding CDS not defined
---