Human (GRCh38.p14)
Description

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

Gene Synonyms

KST1, SGLT6, SMIT2

Location

Scaffold HG2471_PATCH: 96,541-165,111 forward strand.

GRCh38:ML143373.1

View this gene on the primary assembly.

About this gene

This gene has 13 transcripts (splice variants) and 1 gene allele.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000672588.1SLC5A11-2182745675aaENSP00000499965.1
 
Protein coding
Q8WWX8-1 -Ensembl CanonicalGENCODE basic
ENST00000710486.1SLC5A11-2242402675aaENSP00000518306.1
 
Protein coding
--GENCODE basic
ENST00000673269.1SLC5A11-2222399640aaENSP00000500384.1
 
Protein coding
Q8WWX8-2 -GENCODE basic
ENST00000672971.1SLC5A11-2202294605aaENSP00000500955.1
 
Protein coding
Q8WWX8-5 -GENCODE basic
ENST00000672547.1SLC5A11-2172246640aaENSP00000500395.1
 
Protein coding
Q8WWX8-2 -GENCODE basic
ENST00000673441.1SLC5A11-2232214611aaENSP00000500055.1
 
Protein coding
Q8WWX8-3 -GENCODE basic
ENST00000672672.1SLC5A11-2192139605aaENSP00000500207.1
 
Protein coding
Q8WWX8-5 -GENCODE basic
ENST00000672306.1SLC5A11-2152069519aaENSP00000500570.1
 
Protein coding
Q8WWX8-6 -GENCODE basic
ENST00000671711.1SLC5A11-2121919519aaENSP00000500525.1
 
Protein coding
Q8WWX8-6 -GENCODE basic
ENST00000671921.1SLC5A11-21359191aaENSP00000500759.1
 
Protein coding
--CDS 3' incomplete
ENST00000672342.1SLC5A11-216270362aaENSP00000499901.1
 
Nonsense mediated decay
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ENST00000672151.1SLC5A11-214577No protein-
 
Retained intron
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ENST00000673108.1SLC5A11-221475No protein-
 
Retained intron
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