KEGG   Homo sapiens (human): 79581
Entry
79581             CDS       T01001                                 
Symbol
SLC52A2, BVVLS2, D15Ertd747e, GPCR41, GPR172A, HuPAR-1, PAR1, RFT3, RFVT2, hRFT3
Name
(RefSeq) solute carrier family 52 member 2
  KO
K22117  riboflavin transporter 1/3
Organism
hsa  Homo sapiens (human)
Disease
H01903  Brown-Vialetto-Van Laere syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    79581 (SLC52A2)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC52: Riboflavin transporter
   79581 (SLC52A2)
SSDB
Motif
Pfam: SLC52_ribofla_tr
Other DBs
NCBI-GeneID: 79581
NCBI-ProteinID: NP_001240744
OMIM: 607882
HGNC: 30224
Ensembl: ENSG00000185803
UniProt: Q9HAB3
Position
8:144358552..144361272
AA seq 445 aa
MAAPTPARPVLTHLLVALFGMGSWAAVNGIWVELPVVVKELPEGWSLPSYVSVLVALGNL
GLLVVTLWRRLAPGKDEQVPIRVVQVLGMVGTALLASLWHHVAPVAGQLHSVAFLALAFV
LALACCASNVTFLPFLSHLPPRFLRSFFLGQGLSALLPCVLALVQGVGRLECPPAPINGT
PGPPLDFLERFPASTFFWALTALLVASAAAFQGLLLLLPPPPSVPTGELGSGLQVGAPGA
EEEVEESSPLQEPPSQAAGTTPGPDPKAYQLLSARSACLLGLLAATNALTNGVLPAVQSF
SCLPYGRLAYHLAVVLGSAANPLACFLAMGVLCRSLAGLGGLSLLGVFCGGYLMALAVLS
PCPPLVGTSAGVVLVVLSWVLCLGVFSYVKVAASSLLHGGGRPALLAAGVAIQVGSLLGA
VAMFPPTSIYHVFHSRKDCADPCDS
NT seq 1338 nt   +upstreamnt  +downstreamnt
atggcagcacccacgcccgcccgtccggtgctgacccacctgctggtggctctcttcggc
atgggctcctgggctgcggtcaatgggatctgggtggagctacctgtggtggtcaaagag
cttccagagggttggagcctcccctcttacgtctctgtgcttgtggctctggggaacctg
ggtctgctggtggtgaccctctggaggaggctggccccaggaaaggacgagcaggtcccc
atccgggtggtgcaggtgctgggcatggtgggcacagccctgctggcctctctgtggcac
catgtggccccagtggcaggacagttgcattctgtggccttcttagcactggcctttgtg
ctggcactggcatgctgtgcctcgaatgtcactttcctgcccttcttgagccacctgcca
cctcgcttcttacggtcattcttcctgggtcaaggcctgagtgccctgctgccctgcgtg
ctggccctagtgcagggtgtgggccgcctcgagtgcccgccagcccccatcaacggcacc
cctggccccccgctcgacttccttgagcgttttcccgccagcaccttcttctgggcactg
actgcccttctggtcgcttcagctgctgccttccagggtcttctgctgctgttgccgcca
ccaccatctgtacccacaggggagttaggatcaggcctccaggtgggagccccaggagca
gaggaagaggtggaagagtcctcaccactgcaagagccaccaagccaggcagcaggcacc
acccctggtccagaccctaaggcctatcagcttctatcagcccgcagtgcctgcctgctg
ggcctgttggccgccaccaacgcgctgaccaatggcgtgctgcctgccgtgcagagcttt
tcctgcttaccctacgggcgtctggcctaccacctggctgtggtgctgggcagtgctgcc
aatcccctggcctgcttcctggccatgggtgtgctgtgcaggtccttggcagggctgggc
ggcctctctctgctgggcgtgttctgtgggggctacctgatggcgctggcagtcctgagc
ccctgcccgcccctggtgggcacctcggcgggggtggtcctcgtggtgctgtcgtgggtg
ctgtgtcttggcgtgttctcctacgtgaaggtggcagccagctccctgctgcatggcggg
ggccggccggcattgctggcagccggcgtggccatccaggtgggctctctgctcggcgct
gttgctatgttccccccgaccagcatctatcacgtgttccacagcagaaaggactgtgca
gacccctgtgactcctga

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (22)   
   KEGG ORTHOLOGY (1)   
   RefGene (10)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (6)   
   OC (1)   
Protein sequence (31)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (29)   
DNA sequence (66)   
   RefSeq(nuc) (30)   
   GenBank (18)   
   EMBL (18)   
Protein domain (1)   
   Pfam (1)   
All databases (126)   

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