Protein Slc17a8

URN urn:agi-llid:64944
Total Entities 0
Connectivity 46
Name Slc17a8
Description solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8
Notes This gene encodes a vesicular glutamate transporter. The encoded protein transports the neurotransmitter glutamate into synaptic vesicles before it is released into the synaptic cleft. Mutations in this gene are the cause of autosomal-dominant nonsyndromic type 25 deafness. Alternate splicing results in multiple transcript variants.[provided by RefSeq, May 2010]

Ariadne Ontology Neurotransmitter loading
Cl- transport

GO Molecular Function L-glutamate transmembrane transporter activity
symporter activity

GO Cellular Component cell junction
membrane
synapse
synaptic vesicle membrane
integral to membrane
cytoplasmic vesicle
neuron projection

GO Biological Process transmembrane transport
amino acid transmembrane transport
sensory perception of sound
transport
neurotransmitter transport
ion transport
sodium ion transport
L-amino acid transport
L-glutamate transport

Pathway auditory mechanotransduction pathway

Group Neurotransmitter loading
Cl- transport
transmembrane transport
amino acid transmembrane transport
sensory perception of sound
transport
neurotransmitter transport
ion transport
sodium ion transport
L-amino acid transport
L-glutamate transport
L-glutamate transmembrane transporter activity
symporter activity
cell junction
membrane
synapse
synaptic vesicle membrane
integral to membrane
cytoplasmic vesicle
neuron projection

MedScan ID 64944

Hugo ID 20151

Human chromosome position 12q23.1

GenBank ID NC_000012
NM_139319
NP_647480
NM_001145288
NP_001138760
NG_021175
NC_018923
AC_000144
AC026110
AC126308
CH471054
EAW97637
AJ459241
CAD30553
AK128319
BAG54658
BC117229
AAI17230
BC143396
AAI43397
Q8NDX2
HQ258284
ADR83038
NC_000076
NM_182959
NP_892004
AC_000032
AC127279
CH466539
EDL21503
AF510321
AAN74643
AK082743
AK149687
BAE29026
BC042593
AAH42593
Q8BFU8
NC_005106
NM_153725
NP_714947
AC_000075
CH473960
EDM16983
EDM16984
AJ491795
CAD37138
AY117026
AAM50094
Q7TSF2

LocusLink ID 64944
246213
216227
266767

Alias DFNA25
VGLUT3
vesicular glutamate transporter 3
solute carrier family 17 member 8
BC042593
vesicular glutamate transporter-3
SLC17A8
vesicular glutamate transporter III
solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter), member 8
OTTMUSP00000029420
deafness, autosomal dominant 25
OTTMUSP00000043239
cDNA sequence BC042593

Organism Homo sapiens
Mus musculus
Rattus norvegicus

OMIM ID 607557
605583

Unigene ID Hs.116871
Mm.233921
Rn.84876

KEGG ID hsa:246213
mmu:216227
rno:266767

Swiss-Prot Accession Q8NDX2
Q8BFU8
Q7TSF2
B3KXZ6
B7ZKV4
Q17RQ8
Q8K1Q1

GO ID 0005313
0015293
0006811
0006836
0007605
0006814
0055085
0030054
0016021
0043005
0030672
0015807
0015813
0003333
0006810
0031410
0016020
0045202

Swiss-Prot ID VGLU3_HUMAN
VGLU3_MOUSE
VGLU3_RAT

Cell Localization Cytoplasmic vesicle
secretory vesicle
synaptic vesicle membrane
Membrane
Cell junction
synapse
synaptosome
Plasma membrane

IPI ID IPI00168611
IPI00783759
IPI00221470
IPI00200411

Mouse chromosome position 10

Rat chromosome position 7q13

Homologene ID 13584

MGI ID 3039629

RGD ID 628870

Primary Cell Localization Plasma membrane