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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 4 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000264047.2SLC5A7-0015152580aaENSP00000264047.2
 
Protein coding
CCDS2074F5H382 Q2T9H3 Q9GZV3
NM_021815
NP_068587
GENCODE basic
ENST00000409059.1SLC5A7-0022032580aaENSP00000387346.1
 
Protein coding
CCDS2074F5H382 Q2T9H3 Q9GZV3
-GENCODE basic
ENST00000540517.1SLC5A7-2011914475aaENSP00000445351.1
 
Protein coding
F5H382 Q2T9H3 -GENCODE basic

Gene-based displays