KEGG   Homo sapiens (human): 113235
Entry
113235            CDS       T01001                                 
Symbol
SLC46A1, G21, HCP1, HsPCFT, PCFT, hPCFT
Name
(RefSeq) solute carrier family 46 member 1
  KO
K14613  MFS transporter, PCFT/HCP family, solute carrier family 46 (folate transporter), member 1
Organism
hsa  Homo sapiens (human)
Pathway
hsa01523  Antifolate resistance
hsa04977  Vitamin digestion and absorption
hsa04978  Mineral absorption
Disease
H01252  Hereditary folate malabsorption
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09150 Organismal Systems
  09154 Digestive system
   04977 Vitamin digestion and absorption
    113235 (SLC46A1)
   04978 Mineral absorption
    113235 (SLC46A1)
 09160 Human Diseases
  09176 Drug resistance: antineoplastic
   01523 Antifolate resistance
    113235 (SLC46A1)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    113235 (SLC46A1)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC46: Folate transporter
   113235 (SLC46A1)
 Major facilitator superfamily (MFS)
  Organic acid transporters
   Proton coupled folate transporter/heme carrier protein (PCFT/HCP) family [TC:2.A.1.50]
    113235 (SLC46A1)
SSDB
Motif
Pfam: MFS_1 Sugar_tr
Other DBs
NCBI-GeneID: 113235
NCBI-ProteinID: NP_542400
OMIM: 611672
HGNC: 30521
Ensembl: ENSG00000076351
UniProt: Q96NT5
Position
17:complement(28394642..28406592)
AA seq 459 aa
MEGSASPPEKPRARPAAAVLCRGPVEPLVFLANFALVLQGPLTTQYLWHRFSADLGYNGT
RQRGGCSNRSADPTMQEVETLTSHWTLYMNVGGFLVGLFSSTLLGAWSDSVGRRPLLVLA
SLGLLLQALVSVFVVQLQLHVGYFVLGRILCALLGDFGGLLAASFASVADVSSSRSRTFR
MALLEASIGVAGMLASLLGGHWLRAQGYANPFWLALALLIAMTLYAAFCFGETLKEPKST
RLFTFRHHRSIVQLYVAPAPEKSRKHLALYSLAIFVVITVHFGAQDILTLYELSTPLCWD
SKLIGYGSAAQHLPYLTSLLALKLLQYCLADAWVAEIGLAFNILGMVVFAFATITPLMFT
GYGLLFLSLVITPVIRAKLSKLVRETEQGALFSAVACVNSLAMLTASGIFNSLYPATLNF
MKGFPFLLGAGLLLIPAVLIGMLEKADPHLEFQQFPQSP
NT seq 1380 nt   +upstreamnt  +downstreamnt
atggaggggagcgcgagccccccggaaaagccccgcgcccgccctgcggctgccgtgctg
tgccggggcccggtagagccgctggtcttcctggccaactttgccttggtcctgcagggc
ccgctcaccacgcagtatctgtggcaccgcttcagcgccgacctcggctacaatggcacc
cgccaaagggggggctgcagcaaccgcagcgcggaccccaccatgcaggaagtggagacc
cttacctcccactggaccctctacatgaacgtgggcggcttcctggtggggctcttctcg
tccaccctgctgggagcttggagcgacagtgtgggccgccgcccgctgctagtgctggcc
tcgctgggcctgctgctccaggccctagtgtccgtttttgtggtgcagctgcagctccac
gtcggctacttcgtgctgggtcgcatcctttgtgccctcctcggcgacttcggtggcctt
ctggctgctagctttgcgtccgtggcagatgtcagctccagtcgcagccgcaccttccgg
atggccctgctggaagccagcatcggggtggctgggatgctggcaagcctcctcgggggc
cactggctccgggcccagggttatgccaaccccttctggctggccttggccttgctgata
gccatgactctctatgcagctttctgctttggtgagaccttaaaggagccaaagtccacc
cggctcttcacgttccgtcaccaccgatccattgtccagctctatgtggctcccgcccca
gagaagtccaggaaacatttagccctctactcactggccatcttcgtggtgatcactgtg
cactttggggcccaggacatcttaaccctttatgaactaagcacacccctctgctgggac
tccaaactaatcggctatggttctgcagctcagcatctcccctacctcaccagcctgctg
gccctgaagctcctgcagtactgcctggccgatgcctgggtagctgagatcggcctggcc
ttcaacatcctggggatggtggtctttgcctttgccactatcacgcctctcatgttcaca
ggatatgggttgcttttcctgtcattagtcatcacacctgtcatccgggctaaactctcc
aagctggtgagagagacagagcagggtgctctcttttctgctgtggcctgtgtgaatagc
ctggccatgctgacggcctccggcatcttcaactcactctacccagccactctgaacttt
atgaaggggttccccttcctcctgggagctggcctcctgctcatcccggctgttctgatt
gggatgctggaaaaggctgatcctcacctcgagttccagcagtttccccagagcccctga

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