Homo sapiens (human): 9153
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Entry
9153 CDS
T01001
Symbol
SLC28A2, CNT2, HCNT2, HsT17153, SPNT1
Name
(RefSeq) solute carrier family 28 member 2
KO
K11536
pyrimidine nucleoside transport protein
Organism
hsa
Homo sapiens (human)
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
02000 Transporters [BR:
hsa02000
]
9153 (SLC28A2)
Transporters [BR:
hsa02000
]
Solute carrier family (SLC)
SLC28: Na+-coupled nucleoside transporter
9153 (SLC28A2)
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SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Nucleos_tra2_C
Nucleos_tra2_N
Gate
Motif
Other DBs
NCBI-GeneID:
9153
NCBI-ProteinID:
NP_004203
OMIM:
606208
HGNC:
11002
Ensembl:
ENSG00000137860
UniProt:
O43868
Q2M2A7
Q53H72
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All DBs
Position
15:45252234..45277846
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AA seq
658 aa
AA seq
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MEKASGRQSIALSTVETGTVNPGLELMEKEVEPEGSKRTDAQGHSLGDGLGPSTYQRRSR
WPFSKARSFCKTHASLFKKILLGLLCLAYAAYLLAACILNFQRALALFVITCLVIFVLVH
SFLKKLLGKKLTRCLKPFENSRLRLWTKWVFAGVSLVGLILWLALDTAQRPEQLIPFAGI
CMFILILFACSKHHSAVSWRTVFSGLGLQFVFGILVIRTDLGYTVFQWLGEQVQIFLNYT
VAGSSFVFGDTLVKDVFAFQALPIIIFFGCVVSILYYLGLVQWVVQKVAWFLQITMGTTA
TETLAVAGNIFVGMTEAPLLIRPYLGDMTLSEIHAVMTGGFATISGTVLGAFIAFGVDAS
SLISASVMAAPCALASSKLAYPEVEESKFKSEEGVKLPRGKERNVLEAASNGAVDAIGLA
TNVAANLIAFLAVLAFINAALSWLGELVDIQGLTFQVICSYLLRPMVFMMGVEWTDCPMV
AEMVGIKFFINEFVAYQQLSQYKNKRLSGMEEWIEGEKQWISVRAEIITTFSLCGFANLS
SIGITLGGLTSIVPHRKSDLSKVVVRALFTGACVSLISACMAGILYVPRGAEADCVSFPN
TSFTNRTYETYMCCRGLFQSTSLNGTNPPSFSGPWEDKEFSAMALTNCCGFYNNTVCA
NT seq
1977 nt
NT seq
+upstream
nt +downstream
nt
atggagaaagcaagtggaagacagtccattgctctgtccacagtggagactggcacagtg
aacccggggctggagctcatggaaaaagaagtagagcctgagggaagcaagaggactgac
gcacaaggacacagcctgggggatggactgggcccttccacttaccagaggaggagtcgg
tggcctttcagcaaagcaagaagtttctgcaaaacacacgccagcttgttcaagaagatc
ctgttgggcctgttgtgtttggcctatgctgcctatctcctggcagcttgcatcttgaat
ttccagagggcactggccttgtttgtcatcacctgcttggtgatctttgtcctggttcac
tcgtttttgaaaaagctcctgggcaaaaaattaacaagatgtctgaagccctttgaaaac
tcccgcctgaggctttggacgaaatgggtgtttgcaggagtctccttggttggccttata
ctgtggttggctttagacacagcccaaaggccagagcagctgatcccctttgcaggaatc
tgcatgttcatccttatcctctttgcctgctccaaacaccacagcgcagtgtcctggagg
acagtgttttcgggcctaggtcttcaatttgtctttgggatcttggtcatcagaactgat
cttggatatactgtatttcagtggctgggagagcaggtccagattttcctgaactacact
gtggccggctccagttttgtctttggggatacactggtcaaggatgtctttgcttttcag
gccttaccaatcatcattttctttggatgtgtggtgtccattctctactacctgggcctt
gtgcaatgggtagttcagaaggtcgcctggtttttacaaatcactatgggcaccactgct
acagagaccctggctgtggcaggaaacatctttgtgggtatgacagaggcacctctgctc
atccgtccctaccttggggacatgacactctctgaaatccatgcggtgatgactggaggg
tttgccaccatttctggcactgtgctgggagccttcatagcctttggggttgatgcatca
tccctgatttctgcctctgtgatggccgccccttgtgctctcgcctcatcaaagctagcg
tatccggaagtggaggagtccaagttcaagagtgaggagggggtaaagctgccccgtggg
aaggagaggaatgtcctggaagctgccagcaacggagccgtagatgccataggccttgct
actaatgtagcagccaacctgattgcctttttggctgtgttggccttcatcaatgctgcc
ctctcctggctgggggaattggtggacatacaggggctcactttccaggtcatctgctcc
tatctcctaaggcccatggttttcatgatgggtgtagagtggacagactgtccaatggtg
gctgagatggtgggaatcaagttcttcataaatgagtttgtggcttatcagcaactgtct
caatacaagaacaaacgtctctctggaatggaggagtggattgagggagagaaacagtgg
atttctgtgagagctgaaatcattacaacattttcactctgtggatttgccaatcttagt
tccataggaatcacacttggaggcttgacatcaatagtacctcaccggaagagtgacttg
tccaaggttgtggtcagggccctcttcacaggggcctgtgtatcccttatcagtgcctgt
atggcaggaatcctctatgtccccaggggagctgaagctgactgtgtctccttcccaaac
acaagtttcaccaatagaacctatgagacctacatgtgctgcagagggctctttcagagt
acttctctgaatggcaccaaccctccttctttttctggtccctgggaagataaggagttc
agtgctatggcccttactaactgctgtggattctacaacaataccgtctgtgcctaa
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