Human (GRCh38.p14)
Description

solute carrier family 6 member 14 [Source:HGNC Symbol;Acc:HGNC:11047]

Location

Chromosome X: 116,436,606-116,461,458 forward strand.

GRCh38:CM000685.2

About this gene

This gene has 6 transcripts (splice variants), 30 orthologues, 19 paralogues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000598581.3SLC6A14-2024536642aaENSP00000470801.1
 
Protein coding
CCDS14570Q9UN76 NM_007231.5MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P4TSL:1
ENST00000961159.1SLC6A14-2044391595aaENSP00000631218.1
 
Protein coding
--GENCODE Basic
ENST00000905559.1SLC6A14-2033550598aaENSP00000575618.1
 
Protein coding
--GENCODE Basic
ENST00000961161.1SLC6A14-2062198641aaENSP00000631220.1
 
Protein coding
--GENCODE PrimaryGENCODE BasicAPPRIS ALT1
ENST00000961160.1SLC6A14-2051987569aaENSP00000631219.1
 
Protein coding
--GENCODE Basic
ENST00000463626.1SLC6A14-201344No protein-
 
Protein coding CDS not defined
--TSL:3