K05334                      KO                                     

solute carrier family 6 (neurotransmitter transporter) member 19
map04974  Protein digestion and absorption
map04978  Mineral absorption
H00843  Hartnup disorder
H00905  Iminoglycinuria
H01304  Hyperglycinuria
KEGG Orthology (KO) [BR:ko00001]
 09150 Organismal Systems
  09154 Digestive system
   04974 Protein digestion and absorption
    K05334  SLC6A19; solute carrier family 6 (neurotransmitter transporter) member 19
   04978 Mineral absorption
    K05334  SLC6A19; solute carrier family 6 (neurotransmitter transporter) member 19
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters
    K05334  SLC6A19; solute carrier family 6 (neurotransmitter transporter) member 19
   04147 Exosome
    K05334  SLC6A19; solute carrier family 6 (neurotransmitter transporter) member 19
Transporters [BR:ko02000]
 Solute carrier family (SLC)
  SLC6: Sodium- and chloride-dependent neurotransmitter transporter
   K05334  SLC6A19; solute carrier family 6 (neurotransmitter transporter) member 19
Exosome [BR:ko04147]
 Exosomal proteins
  Exosomal proteins of other body fluids (saliva and urine)
   K05334  SLC6A19; solute carrier family 6 (neurotransmitter transporter) member 19
Other DBs
GO: 0005330
TC: 2.A.22.6.3
HSA: 340024(SLC6A19)
PTR: 100612671(SLC6A19)
PPS: 100990294(SLC6A19)
GGO: 101128098(SLC6A19)
PON: 100173524(SLC6A19)
NLE: 100596167(SLC6A19)
MCC: 100424683(SLC6A19)
MCF: 102140013(SLC6A19)
CSAB: 103214924(SLC6A19)
CATY: 105600702(SLC6A19)
PANU: 101024082(SLC6A19)
RRO: 104668702(SLC6A19)
RBB: 108513716(SLC6A19)
TFN: 117064698(SLC6A19)
PTEH: 111528339(SLC6A19)
CJC: 100395048(SLC6A19)
SBQ: 101048016(SLC6A19)
MMUR: 105876454(SLC6A19)
MMU: 74338(Slc6a19)
MCAL: 110308202(Slc6a19)
MPAH: 110329107(Slc6a19)
RNO: 664630(Slc6a19)
MCOC: 116083180(Slc6a19)
MUN: 110545361(Slc6a19)
CGE: 100762288(Slc6a19)
PLEU: 114696101(Slc6a19)
NGI: 103749671(Slc6a19)
HGL: 101706596(Slc6a19)
CPOC: 100715186(Slc6a19)
CCAN: 109698257(Slc6a19)
OCU: 100302437(SLC6A19)
OPI: 101530660(SLC6A19)
TUP: 102498528(SLC6A19)
CFA: 100683912(SLC6A19)
VVP: 112935446(SLC6A19)
VLG: 121477528(SLC6A19)
AML: 100479160(SLC6A19)
UMR: 103679265(SLC6A19)
UAH: 113260785(SLC6A19)
ORO: 101386033(SLC6A19)
ELK: 111153453
MPUF: 101690694(SLC6A19)
EJU: 114198564(SLC6A19)
MLX: 118006194(SLC6A19)
PYU: 121040751(SLC6A19)
PBG: 122495793(SLC6A19)
PTG: 102965266(SLC6A19)
PPAD: 109267685
AJU: 106985109(SLC6A19)
HHV: 120235624(SLC6A19)
BTA: 100337416(SLC6A19)
BOM: 102268976(SLC6A19)
BIU: 109574754(SLC6A19)
BBUB: 102415755(SLC6A19)
CHX: 102188256(SLC6A19)
OAS: 114118762(SLC6A19)
ODA: 120879242(SLC6A19)
CCAD: 122454582(SLC6A19)
SSC: 641346(SLC6A19)
CFR: 102509526(SLC6A19)
CBAI: 105081215(SLC6A19)
CDK: 105102194(SLC6A19)
BACU: 103002801(SLC6A19)
LVE: 103088450(SLC6A19)
OOR: 101290050
DLE: 111178484(SLC6A19)
PCAD: 102981180
PSIU: 116752227(SLC6A19)
ECB: 100069470(SLC6A19)
EPZ: 103553583(SLC6A19)
EAI: 106835878(SLC6A19)
MYB: 102245862(SLC6A19)
MYD: 102769398(SLC6A19)
MMYO: 118657066(SLC6A19)
MLF: 102423517(SLC6A19)
MNA: 107536762(SLC6A19)
PKL: 118703498(SLC6A19)
HAI: 109371678(SLC6A19)
DRO: 112321106(SLC6A19)
SHON: 118998654(SLC6A19)
AJM: 119043405(SLC6A19)
PDIC: 114506003(SLC6A19)
MMF: 118642450(SLC6A19)
RFQ: 117025333(SLC6A19)
PALE: 102891152(SLC6A19)
PGIG: 120586304(SLC6A19)
PVP: 105301318(SLC6A19)
RAY: 107499980(SLC6A19)
MJV: 108408616(SLC6A19)
TOD: 119260484(SLC6A19)
LAV: 100676875(SLC6A19)
TMU: 101342012
MDO: 100618267(SLC6A19)
GAS: 123238021(SLC6A19)
SHR: 100933103(SLC6A19)
PCW: 110201213(SLC6A19)
OAA: 100074607(SLC6A19)
GGA: 420971(SLC6A19)
PCOC: 116226540(SLC6A19)
MGP: 100546492(SLC6A19)
CJO: 107309458(SLC6A19)
NMEL: 110394863(SLC6A19)
APLA: 101791865(SLC6A19)
ACYG: 106045015(SLC6A19)
TGU: 100223404(SLC6A19)
LSR: 110469749(SLC6A19)
SCAN: 103825943(SLC6A19)
PMOA: 120502987(SLC6A19)
OTC: 121337773(SLC6A19)
PRUF: 121358430(SLC6A19)
GFR: 102043780(SLC6A19)
FAB: 101819871(SLC6A19)
PHI: 102108309(SLC6A19)
PMAJ: 107200980(SLC6A19)
CCAE: 111925331(SLC6A19)
CCW: 104685845(SLC6A19)
ETL: 114060992(SLC6A19)
FPG: 101915935(SLC6A19)
FCH: 102047372
CLV: 102092964(SLC6A19)
EGZ: 104128508(SLC6A19)
NNI: 104013408(SLC6A19)
ACUN: 113476610(SLC6A19)
TALA: 104359779(SLC6A19)
PADL: 103922328(SLC6A19)
AAM: 106492854(SLC6A19)
AROW: 112971805(SLC6A19)
NPD: 112947537(SLC6A19)
DNE: 112983039(SLC6A19)
ASN: 102383088(SLC6A19)
AMJ: 102563441(SLC6A19)
CPOO: 109313698(SLC6A19)
GGN: 109291960
PSS: 102447644(SLC6A19)
CMY: 102929740
CPIC: 101946921(SLC6A19)
TST: 117872743(SLC6A19)
CABI: 116817009(SLC6A19)
MRV: 120397937(SLC6A19)
ACS: 100559327(slc6a19)
PVT: 110080905(SLC6A19)
PBI: 103056380(SLC6A19)
PMUR: 107292117(SLC6A19)
PGUT: 117662413(SLC6A19)
VKO: 123029736
PMUA: 114601046
ZVI: 118090404(SLC6A19)
GJA: 107123974(SLC6A19)
XLA: 447481(slc6a19.S) 447504(slc6a19.L)
XTR: 100145739(slc6a19)
NPR: 108797280(SLC6A19)
DRE: 100334171(slc6a19a.2) 326030(slc6a19b) 553256(slc6a19a.1)
IPU: 108270036(Slc6a19) 108274802
LOC: 102689620(slc6a19)
LCM: 102361061(SLC6A19)
CMK: 103176218
RTP: 109912179(slc6a19)
CIN: 100186059
HAZT: 108670468
BGT: 106069830
PMAX: 117339401
 » show all
Seow HF, Broer S, Broer A, Bailey CG, Potter SJ, Cavanaugh JA, Rasko JE
Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19.
Nat Genet 36:1003-7 (2004)
Broer S
Amino acid transport across mammalian intestinal and renal epithelia.
Physiol Rev 88:249-86 (2008)
Broer S
Apical transporters for neutral amino acids: physiology and pathophysiology.
Physiology (Bethesda) 23:95-103 (2008)

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