Human (GRCh37.p13)
Description

solute carrier family 5 (sodium/choline cotransporter), member 7 [Source:HGNC Symbol;Acc:14025]

Gene Synonyms

CHT, CHT1, HMN7A, hCHT

Location

Chromosome 2: 108,602,979-108,630,450 forward strand.

GRCh37:CM000664.1

About this gene

This gene has 3 transcripts (splice variants) and is associated with 5 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000264047.2SLC5A7-0015152580aaENSP00000264047.2
 
Protein coding
CCDS2074F5H382 Q2T9H3 Q9GZV3
NM_021815.2GENCODE basic
ENST00000409059.1SLC5A7-0022032580aaENSP00000387346.1
 
Protein coding
CCDS2074F5H382 Q2T9H3 Q9GZV3
-GENCODE basic
ENST00000540517.1SLC5A7-2011914475aaENSP00000445351.1
 
Protein coding
F5H382 Q2T9H3 -GENCODE basic
As of the latest update in March 2020 we are not supporting data for species other than human on this GRCh37 site and the view you wish to use is disabled.

You can read more about why we have done this on our blog.

You can still view this page on the following archive resources:

1. The Ensembl 75 archive represents a code and data freeze taken in February 2014.

2. The GRCh37 archive represents a code and data freeze taken in January 2019.