SLC6A19

GENE INFORMATION

? »

Gene name

SLC6A19

Synonyms

Description

Solute carrier family 6 (neutral amino acid transporter), member 19 (HGNC Symbol)

Entrez gene summary

This gene encodes a system B(0) transmembrane protein that actively transports most neutral amino acids across the apical membrane of epithelial cells. Mutations in this gene result in Hartnup disorder. [provided by RefSeq, Jul 2008]

Chromosome

5

Cytoband

p15.33

Chromosome location (bp)

1201710 - 1225232

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000174358 (version 75.37)

Entrez gene

340024

UniProt

Q695T7 (UniProt - Evidence at protein level)

neXtProt

NX_Q695T7

Antibodypedia

SLC6A19 antibodies
 

PROTEIN VIEW

? »
 
 
 
SLC6A19-001
 
SLC6A19-002
 
 
 
 
 

PROTEIN INFORMATION

? »

Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

SLC6A19-001 ENSP00000305302
ENST00000304460
Q695T7
Show all »
Show » Show » 634 71.1 No >9
SLC6A19-002 ENSP00000425701
ENST00000515652
E9PD72
Show all »
Show » Show » 354 39.4 No 2