KEGG   Homo sapiens (human): 5002
Entry
5002              CDS       T01001                                 
Symbol
SLC67A1, BWR1A, BWSCR1A, HET, IMPT1, ITM, ORCTL2, SLC22A18, SLC22A1L, TSSC5, p45-BWR1A
Name
(RefSeq) solute carrier family 67 member 1
  KO
K08214  MFS transporter, DHA1 family, solute carrier family 67, member 1
Organism
hsa  Homo sapiens (human)
Disease
H00031  Breast cancer
H00037  Rhabdomyosarcoma
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    5002 (SLC67A1)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC67: Organic cation transporter-like
   5002 (SLC67A1)
SSDB
Motif
Pfam: MFS_1 MFS_2 MFS_3
Other DBs
NCBI-GeneID: 5002
NCBI-ProteinID: NP_002546
OMIM: 602631
HGNC: 10964
Ensembl: ENSG00000110628
UniProt: Q96BI1
Position
11:2899691..2925246
AA seq 424 aa
MQGARAPRDQGRSPGRMSALGRSSVILLTYVLAATELTCLFMQFSIVPYLSRKLGLDSIA
FGYLQTTFGVLQLLGGPVFGRFADQRGARAALTLSFLAALALYLLLAAASSPALPGVYLL
FASRLPGALMHTLPAAQMVITDLSAPEERPAALGRLGLCFGVGVILGSLLGGTLVSAYGI
QCPAILAALATLLGAVLSFTCIPASTKGAKTDAQAPLPGGPRASVFDLKAIASLLRLPDV
PRIFLVKVASNCPTGLFMVMFSIISMDFFQLEAAQAGYLMSFFGLLQMVTQGLVIGQLSS
HFSEEVLLRASVLVFIVVGLAMAWMSSVFHFCLLVPGLVFSLCTLNVVTDSMLIKAVSTS
DTGTMLGLCASVQPLLRTLGPTVGGLLYRSFGVPVFGHVQVAINTLVLLVLWRKPMPQRK
DKVR
NT seq 1275 nt   +upstreamnt  +downstreamnt
atgcagggagctcgggctcccagggaccagggccggtcccccggcaggatgagcgctcta
ggccggtcctcggtcatcttgcttacctacgtgctggccgccacagaacttacctgcctc
ttcatgcagttctccatcgtgccatacctgtctcggaaactgggcctggattccattgcc
ttcggctacctgcaaaccaccttcggggtgctgcagctgctgggcgggccggtatttggc
aggttcgcagaccagcgcggggcgcgggcggcgctcacgctctccttcctggctgccttg
gcgctctacctgctcctggcggccgcctccagcccggccctgcccggggtctacctgctc
ttcgcctcgcgcctgcccggagcgctcatgcacacgctgccagccgcccagatggtcatc
acggacctgtcggcacccgaggagcggcccgcggccctgggccggctgggcctctgcttc
ggcgtcggagtcatcctcggctccctgctgggcgggaccctggtctccgcgtacgggatt
cagtgcccggccatcctggctgccctggccaccctcctgggagctgtcctcagcttcacc
tgcatccccgccagcaccaaaggggccaaaactgacgcccaggctccactgccaggcggc
ccccgggccagtgtgttcgacctgaaggccatcgcctccctgctgcggctgccagacgtc
ccgaggatcttcctggtgaaggtggcctccaactgccccacagggctcttcatggtcatg
ttctccatcatctccatggacttcttccagctggaggccgcccaagctggctacctcatg
tccttcttcgggctcctccagatggtgacccagggcctggtcatcgggcagctgagcagc
cacttctcggaggaggtgctgctccgggccagcgtgctggtcttcatcgtggtgggcctg
gccatggcctggatgtccagcgtcttccacttctgcctcctggtgcccggcctggtgttc
agcctctgcaccctcaacgtggtcaccgacagcatgctgatcaaggctgtctccacctcg
gacacagggaccatgctgggcctctgcgcctctgtacaaccactgctccgaactctggga
cccacggtcggcggcctcctgtaccgcagctttggcgtccccgtcttcggccacgtgcag
gttgctatcaatacccttgtcctcctggtcctctggaggaaacctatgccccagaggaag
gacaaagtccggtga

  All links  
Disease (4)   
   OMIM (4)   
Gene (17)   
   RefGene (7)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (5)   
   OC (1)   
Protein sequence (26)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (24)   
DNA sequence (54)   
   RefSeq(nuc) (24)   
   GenBank (15)   
   EMBL (15)   
Protein domain (3)   
   Pfam (3)   
All databases (104)   

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