Human (GRCh38.p14)
Description

solute carrier family 49 member 3 [Source:HGNC Symbol;Acc:HGNC:26177]

Gene Synonyms

FLJ22269, LP2561, MFSD7

Location

Chromosome 4: 681,829-689,271 reverse strand.

GRCh38:CM000666.2

About this gene

This gene has 9 transcripts (splice variants), 201 orthologues and 4 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000322224.9SLC49A3-2011833559aaENSP00000320234.4
 
Protein coding
CCDS3338Q6UXD7-2 NM_032219.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P4TSL:1
ENST00000404286.6SLC49A3-2031826560aaENSP00000384616.2
 
Protein coding
CCDS75086Q6UXD7-1 -GENCODE basicAPPRIS ALT2TSL:1
ENST00000503156.5SLC49A3-2041632420aaENSP00000425753.1
 
Protein coding
D6RIZ6 -GENCODE basicTSL:5
ENST00000347950.9SLC49A3-2021599441aaENSP00000307545.5
 
Protein coding
CCDS77883Q6UXD7-3 -GENCODE basicTSL:2
ENST00000515118.5SLC49A3-2091556463aaENSP00000423204.1
 
Protein coding
CCDS93459D6R9R0 -GENCODE basicTSL:5
ENST00000507165.5SLC49A3-205938217aaENSP00000424556.1
 
Protein coding
D6RB07 -TSL:3CDS 3' incomplete
ENST00000512249.1SLC49A3-206653199aaENSP00000425038.1
 
Protein coding
D6RED0 -TSL:3CDS 3' incomplete
ENST00000513740.1SLC49A3-208498No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000512400.1SLC49A3-2071472No protein-
 
Retained intron
--TSL:2