Human (GRCh38.p14)
Description

solute carrier family 5 member 11 [Source:HGNC Symbol;Acc:HGNC:23091]

Gene Synonyms

KST1, SGLT6, SMIT2

Location
About this transcript

This transcript has 15 exons, is annotated with 22 domains and features, is associated with 29932 variant alleles and maps to 459 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000424767.7SLC5A11-2022402675aaENSP00000416782.3
 
Protein coding
CCDS10625Q8WWX8-1 NM_001352248.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:2
ENST00000347898.7SLC5A11-2012745675aaENSP00000289932.3
 
Protein coding
CCDS10625Q8WWX8-1 -GENCODE basicAPPRIS P1TSL:1
ENST00000567758.6SLC5A11-2082263640aaENSP00000454401.1
 
Protein coding
CCDS58437Q8WWX8-2 -GENCODE basicTSL:5
ENST00000565769.5SLC5A11-2072214611aaENSP00000457179.1
 
Protein coding
CCDS58439Q8WWX8-3 -GENCODE basicTSL:1
ENST00000568579.6SLC5A11-2092156605aaENSP00000456234.1
 
Protein coding
CCDS58438Q8WWX8-5 -GENCODE basicTSL:5
ENST00000569071.2SLC5A11-2101936519aaENSP00000456376.1
 
Protein coding
CCDS58440Q8WWX8-6 -GENCODE basicTSL:5
ENST00000569520.5SLC5A11-21159191aaENSP00000454732.1
 
Protein coding
H3BN85 -TSL:4CDS 3' incomplete
ENST00000488922.6SLC5A11-203270362aaENSP00000458806.1
 
Nonsense mediated decay
I3L1G0 -TSL:5
ENST00000545376.6SLC5A11-204250954aaENSP00000441384.2
 
Nonsense mediated decay
A0A8J9ASH1 -TSL:2
ENST00000564125.1SLC5A11-205577No protein-
 
Retained intron
--TSL:3
ENST00000565586.1SLC5A11-206475No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 15, Coding exons: 13, Transcript length: 2,156 bps, Translation length: 605 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q8WWX8

CCDS

This transcript is a member of the Human CCDS set: CCDS58438

Transcript Support Level (TSL)

TSL:5

Version

ENST00000568579.6

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.