KEGG   Homo sapiens (human): 55065
Entry
55065             CDS       T01001                                 
Symbol
SLC52A1, GPCR42, GPR172B, PAR2, RBFVD, RFT1, RFVT1, hRFT1, huPAR-2
Name
(RefSeq) solute carrier family 52 member 1
  KO
K22117  riboflavin transporter 1/3
Organism
hsa  Homo sapiens (human)
Disease
H02544  Riboflavin deficiency
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    55065 (SLC52A1)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC52: Riboflavin transporter
   55065 (SLC52A1)
SSDB
Motif
Pfam: DUF1011
Other DBs
NCBI-GeneID: 55065
NCBI-ProteinID: NP_001098047
OMIM: 607883
HGNC: 30225
Ensembl: ENSG00000132517
UniProt: Q9NWF4
Position
17:complement(5032602..5042414)
AA seq 448 aa
MAAPTLGRLVLTHLLVALFGMGSWAAVNGIWVELPVVVKDLPEGWSLPSYLSVVVALGNL
GLLVVTLWRQLAPGKGEQVPIQVVQVLSVVGTALLAPLWHHVAPVAGQLHSVAFLTLALV
LAMACCTSNVTFLPFLSHLPPPFLRSFFLGQGLSALLPCVLALVQGVGRLECPPAPTNGT
SGPPLDFPERFPASTFFWALTALLVTSAAAFRGLLLLLPSLPSVTTGGSGPELQLGSPGA
EEEEKEEEEALPLQEPPSQAAGTIPGPDPEAHQLFSAHGAFLLGLMAFTSAVTNGVLPSV
QSFSCLPYGRLAYHLAVVLGSAANPLACFLAMGVLCRSLAGLVGLSLLGMLFGAYLMALA
ILSPCPPLVGTTAGVVLVVLSWVLCLCVFSYVKVAASSLLHGGGRPALLAAGVAIQVGSL
LGAGAMFPPTSIYHVFQSRKDCVDPCGP
NT seq 1347 nt   +upstreamnt  +downstreamnt
atggcagcacccacgctgggccgtctggtgctgacccacctgctggtggccctttttggc
atgggctcctgggctgctgtgaacgggatctgggtggagctgcctgtggtggtaaaagac
cttccagagggttggagcctcccctcatacctctctgtggttgtggcgctgggaaacctg
ggtctgctggtggtgaccctgtggaggcagctggccccgggcaagggcgagcaggtcccc
atccaggtggtacaggtgctgagtgtagtgggcacagccctgctggcccctctgtggcac
cacgtggccccagtggcagggcagctccactctgtggccttcctaactctggccttggtg
ttggcaatggcctgttgtacctctaatgtcactttcctgcccttcctgagccacctgcca
cctcctttcttacggtctttcttcctgggtcagggtctcagtgccctactcccctgtgtg
ctggccctagtgcaaggtgtgggccgcctcgagtgcccaccagcgcccaccaatggcacc
tctgggcctcccctcgacttccctgagcgttttcctgccagcaccttcttctgggcactg
actgcccttctggtcacttcagctgccgccttccggggtctcctgttgctgttgccatca
ctaccctctgtaaccacagggggctcagggcctgaacttcaactgggatccccaggagca
gaggaggaagagaaggaggaagaagaggctttgccattgcaggagccaccgagccaggca
gcaggcaccatccctggcccagaccctgaggcccatcagctgttctcagcccatggtgcc
ttcctgctgggcctgatggccttcaccagtgccgtgaccaatggcgtgctgccttctgtg
cagagcttttcctgtttgccctatgggcgcctggcctaccacctggctgtggtgctgggc
agtgccgccaacccccttgcctgcttcctggccatgggcgtgctgtgcaggtccctggca
gggctggttggtctttctctgctgggcatgctctttggggcctacctgatggcactggca
atcctgagcccctgcccacccctggtgggcaccactgcaggggtggtccttgtggtgctg
tcgtgggtgctgtgtctgtgtgtgttctcatatgtgaaggtggctgcaagctccctgctg
catggtgggggtcggccggcattgctggcagctggtgtggccatccaagtgggctccctg
cttggtgccggtgccatgttccctcccaccagcatctaccacgtgtttcaaagcagaaag
gactgtgtagacccctgtggcccctga

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Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (16)   
   KEGG ORTHOLOGY (1)   
   RefGene (9)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (1)   
   OC (1)   
Protein sequence (10)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (8)   
DNA sequence (28)   
   RefSeq(nuc) (8)   
   GenBank (10)   
   EMBL (10)   
Protein domain (1)   
   Pfam (1)   
All databases (61)   

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