Description

solute carrier family 5 (sodium/multivitamin and iodide cotransporter), member 6 [Source:HGNC Symbol;Acc:HGNC:11041]

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), 73 orthologues, 10 paralogues, is a member of 5 Ensembl protein families and is associated with 113 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
SLC5A6-001ENST000003105743231635aaENSP00000310208
 
Protein coding
CCDS1740Q9Y289 NM_021095
NP_066918
TSL:1GENCODE basicAPPRIS P1
SLC5A6-003ENST000004080412230635aaENSP00000384853
 
Protein coding
CCDS1740Q9Y289 -TSL:1GENCODE basicAPPRIS P1
SLC5A6-004ENST00000412471917193aaENSP00000403851
 
Protein coding
-E7EMX0 -CDS 3' incompleteTSL:5
SLC5A6-005ENST0000041440874178aaENSP00000404032
 
Protein coding
-E7EW41 -CDS 3' incompleteTSL:5
SLC5A6-006ENST00000401463732147aaENSP00000384265
 
Protein coding
-E7EW78 -CDS 3' incompleteTSL:3
SLC5A6-009ENST00000432106725133aaENSP00000411536
 
Protein coding
-E7ENG0 -CDS 3' incompleteTSL:3
SLC5A6-007ENST00000426119676115aaENSP00000401347
 
Protein coding
-E7ERE1 -CDS 3' incompleteTSL:3
SLC5A6-011ENST0000043018659939aaENSP00000399299
 
Protein coding
-E7EXC0 -CDS 3' incompleteTSL:4
SLC5A6-012ENST0000042851857059aaENSP00000402903
 
Protein coding
-E7EP02 -CDS 3' incompleteTSL:4
SLC5A6-010ENST0000044273154227aaENSP00000412115
 
Protein coding
-Q9HD19 -CDS 3' incompleteTSL:4
SLC5A6-008ENST00000445802871153aaENSP00000411361
 
Nonsense mediated decay
-E7ENN0 -TSL:5
SLC5A6-017ENST00000461319598No protein-
 
Processed transcript
---TSL:3
SLC5A6-002ENST000004887433174No protein-
 
Retained intron
--NR_028323
TSL:2
SLC5A6-018ENST000004617572307No protein-
 
Retained intron
---TSL:2
SLC5A6-014ENST00000476319842No protein-
 
Retained intron
---TSL:3
SLC5A6-015ENST00000492069705No protein-
 
Retained intron
---TSL:3
SLC5A6-013ENST00000464538664No protein-
 
Retained intron
---TSL:4
SLC5A6-016ENST00000481751615No protein-
 
Retained intron
---TSL:2

Gene-based displays