Human (GRCh38.p14)
Description

solute carrier family 5 member 6 [Source:HGNC Symbol;Acc:HGNC:11041]

Gene Synonyms

SMVT

Location

Chromosome 2: 27,199,587-27,212,958 reverse strand.

GRCh38:CM000664.2

About this gene

This gene has 18 transcripts (splice variants), 271 orthologues, 11 paralogues and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000310574.8SLC5A6-2013213635aaENSP00000310208.3
 
Protein coding
CCDS1740Q9Y289 NM_021095.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000408041.5SLC5A6-2032230635aaENSP00000384853.1
 
Protein coding
CCDS1740Q9Y289 -GENCODE basicAPPRIS P1TSL:1
ENST00000412471.5SLC5A6-204917193aaENSP00000403851.1
 
Protein coding
E7EMX0 -TSL:5CDS 3' incomplete
ENST00000414408.5SLC5A6-20574178aaENSP00000404032.1
 
Protein coding
E7EW41 -TSL:5CDS 3' incomplete
ENST00000401463.5SLC5A6-202732147aaENSP00000384265.1
 
Protein coding
E7EW78 -TSL:3CDS 3' incomplete
ENST00000432106.5SLC5A6-209725133aaENSP00000411536.1
 
Protein coding
E7ENG0 -TSL:3CDS 3' incomplete
ENST00000426119.5SLC5A6-206676115aaENSP00000401347.1
 
Protein coding
E7ERE1 -TSL:3CDS 3' incomplete
ENST00000430186.5SLC5A6-20859938aaENSP00000399299.1
 
Protein coding
E7EXC0 -TSL:4CDS 3' incomplete
ENST00000428518.5SLC5A6-20757058aaENSP00000402903.1
 
Protein coding
E7EP02 -TSL:4CDS 3' incomplete
ENST00000442731.1SLC5A6-21054227aaENSP00000412115.1
 
Protein coding
Q9HD19 -TSL:4CDS 3' incomplete
ENST00000445802.5SLC5A6-211871153aaENSP00000411361.1
 
Nonsense mediated decay
E7ENN0 -TSL:5
ENST00000461319.5SLC5A6-212598No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000488743.6SLC5A6-2173174No protein-
 
Retained intron
--TSL:2
ENST00000461757.1SLC5A6-2132307No protein-
 
Retained intron
--TSL:2
ENST00000476319.1SLC5A6-215842No protein-
 
Retained intron
--TSL:3
ENST00000492069.5SLC5A6-218705No protein-
 
Retained intron
--TSL:3
ENST00000464538.1SLC5A6-214664No protein-
 
Retained intron
--TSL:4
ENST00000481751.5SLC5A6-216615No protein-
 
Retained intron
--TSL:2