Human (GRCh38.p14)
Description

solute carrier family 66 member 3 [Source:HGNC Symbol;Acc:HGNC:28503]

Gene Synonyms

C2ORF22, MGC33602, PQLC3

Location

Chromosome 2: 11,155,198-11,178,870 forward strand.

GRCh38:CM000664.2

About this gene

This gene has 10 transcripts (splice variants), 200 orthologues and 1 paralogue.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000295083.8SLC66A3-2011717202aaENSP00000295083.3
 
Protein coding
CCDS1679Q8N755-1 NM_152391.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000441908.6SLC66A3-2041784188aaENSP00000406148.2
 
Protein coding
CCDS62856Q8N755-2 -GENCODE basicTSL:2
ENST00000428481.1SLC66A3-20383182aaENSP00000416170.1
 
Protein coding
H7C493 -TSL:2CDS 5' incomplete
ENST00000402361.5SLC66A3-202696120aaENSP00000384129.1
 
Protein coding
CCDS62857B5MC27 -GENCODE basicTSL:2
ENST00000445402.5SLC66A3-205565181aaENSP00000410430.1
 
Protein coding
C9J4B6 -TSL:4CDS 3' incomplete
ENST00000445921.5SLC66A3-206928169aaENSP00000406587.1
 
Nonsense mediated decay
G5E9P4 -TSL:5
ENST00000476787.1SLC66A3-208469No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000487471.1SLC66A3-209466No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000464700.5SLC66A3-207453No protein-
 
Retained intron
--TSL:2
ENST00000496444.1SLC66A3-210388No protein-
 
Retained intron
--TSL:3