KEGG T01001: 340024

Homo sapiens (human): 340024

Entry

340024 CDS T01001

Gene name

SLC6A19, B0AT1, HND

Definition

solute carrier family 6 (neutral amino acid transporter), member 19

Orthology

K05334

solute carrier family 6 (neurotransmitter transporter) member 19

Organism

hsa Homo sapiens (human)

Pathway

hsa04974	Protein digestion and absorption
hsa04978	Mineral absorption

Disease

H00843	Hartnup disorder
H00905	Iminoglycinuria
H01304	Hyperglycinuria

Class

Organismal Systems; Digestive system; Protein digestion and absorption [PATH:hsa04974]
Organismal Systems; Digestive system; Mineral absorption [PATH:hsa04978]

SSDB

Motif

Pfam:

SNF

Other DBs

NCBI-GI:

NCBI-GeneID:

OMIM:

HGNC:

HPRD:

Ensembl:

Vega:

UniProt:

Position

5p15.33

AA seq 634 aa
MVRLVLPNPGLDARIPSLAELETIEQEEASSRPKWDNKAQYMLTCLGFCVGLGNVWRFPY
LCQSHGGGAFMIPFLILLVLEGIPLLYLEFAIGQRLRRGSLGVWSSIHPALKGLGLASML
TSFMVGLYYNTIISWIMWYLFNSFQEPLPWSDCPLNENQTGYVDECARSSPVDYFWYRET
LNISTSISDSGSIQWWMLLCLACAWSVLYMCTIRGIETTGKAVYITSTLPYVVLTIFLIR
GLTLKGATNGIVFLFTPNVTELAQPDTWLDAGAQVFFSFSLAFGGLISFSSYNSVHNNCE
KDSVIVSIINGFTSVYVAIVVYSVIGFRATQRYDDCFSTNILTLINGFDLPEGNVTQENF
VDMQQRCNASDPAAYAQLVFQTCDINAFLSEAVEGTGLAFIVFTEAITKMPLSPLWSVLF
FIMLFCLGLSSMFGNMEGVVVPLQDLRVIPPKWPKEVLTGLICLGTFLIGFIFTLNSGQY
WLSLLDSYAGSIPLLIIAFCEMFSVVYVYGVDRFNKDIEFMIGHKPNIFWQVTWRVVSPL
LMLIIFLFFFVVEVSQELTYSIWDPGYEEFPKSQKISYPNWVYVVVVIVAGVPSLTIPGY
AIYKLIRNHCQKPGDHQGLVSTLSTASMNGDLKY

NT seq 1905 nt +upstreamnt +downstreamnt
atggtgaggctcgtgctgcccaaccccggcctagacgcccggatcccgtccctggctgag
ctggagaccatcgagcaggaggaggccagctcccggccgaagtgggacaacaaggcgcag
tacatgctcacctgcctgggcttctgcgtgggcctcggcaacgtgtggcgcttcccctac
ctgtgtcagagccacggaggaggagccttcatgatcccgttcctcatcctgctggtcctg
gagggcatccccctgctgtacctggagttcgccatcgggcagcggctgcggcggggcagc
ctgggtgtgtggagctccatccacccggccctgaagggcctaggcctggcctccatgctc
acgtccttcatggtgggactgtattacaacaccatcatctcctggatcatgtggtactta
ttcaactccttccaggagcctctgccctggagcgactgcccgctcaacgagaaccagaca
gggtatgtggacgagtgcgccaggagctcccctgtggactacttctggtaccgagagacg
ctcaacatctccacgtccatcagcgactcgggctccatccagtggtggatgctgctgtgc
ctggcctgcgcatggagcgtcctgtacatgtgcaccatccgcggcatcgagaccaccggg
aaggccgtgtacatcacctccacgctgccctatgtcgtcctgaccatcttcctcatccga
ggcctgacgctgaagggcgccaccaatggcatcgtcttcctcttcacgcccaacgtcacg
gagctggcccagccggacacctggctggacgcgggcgcacaggtcttcttctccttctcc
ctggccttcgggggcctcatctccttctccagctacaactctgtgcacaacaactgcgag
aaggactcggtgattgtgtccatcatcaacggcttcacatcggtgtatgtggccatcgtg
gtctactccgtcattgggttccgcgccacacagcgctacgacgactgcttcagcacgaac
atcctgaccctcatcaacgggttcgacctgcctgaaggcaacgtgacccaggagaacttt
gtggacatgcagcagcggtgcaacgcctccgaccccgcggcctacgcgcagctggtgttc
cagacctgcgacatcaacgccttcctctcagaggccgtggagggcacaggcctggccttc
atcgtcttcaccgaggccatcaccaagatgccgttgtccccactgtggtctgtgctcttc
ttcattatgctcttctgcctggggctgtcatctatgtttgggaacatggagggcgtcgtt
gtgcccctgcaggacctcagagtcatccccccgaagtggcccaaggaggtgctcacaggc
ctcatctgcctggggacattcctcattggcttcatcttcacgctgaactccggccagtac
tggctctccctgctggacagctatgccggctccattcccctgctcatcatcgccttctgc
gagatgttctctgtggtctacgtgtacggtgtggacaggttcaataaggacatcgagttc
atgatcggccacaagcccaacatcttctggcaagtcacgtggcgcgtggtcagccccctg
ctcatgctgatcatcttcctcttcttcttcgtggtagaggtcagtcaggagctgacctac
agcatctgggaccctggctacgaggaatttcccaaatcccagaagatctcctacccgaac
tgggtgtatgtggtggtggtgattgtggctggagtgccctccctcaccatccctggctat
gccatctacaagctcatcaggaaccactgccagaagccaggggaccatcaggggctggtg
agcacactgtccacagcctccatgaacggggacctgaagtactga

All links

Ontology (1)   
   KEGG BRITE (1)   
Pathway (2)   
   KEGG PATHWAY (2)   
Disease (7)   
   KEGG DISEASE (3)   
   OMIM (4)   
Genome (1)   
   KEGG GENOME (1)   
Gene (16)   
   KEGG ORTHOLOGY (1)   
   NCBI-Gene (1)   
   NCBI-GI (8)   
   UniGene (1)   
   HGNC (1)   
   HPRD (1)   
   ENSEMBL-HSA (1)   
   OC (1)   
   VEGA (1)   
Protein sequence (2)   
   UniProt (1)   
   RefSeq(pep) (1)   
DNA sequence (21)   
   RefSeq(nuc) (1)   
   GenBank (10)   
   EMBL (10)   
Protein domain (1)   
   Pfam (1)   
All databases (51)   

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