KEGG   Homo sapiens (human): 2030
Entry
2030              CDS       T01001                                 

Gene name
SLC29A1, ENT1
Definition
(RefSeq) solute carrier family 29 member 1 (Augustine blood group)
  KO
K15014  solute carrier family 29 (equilibrative nucleoside transporter), member 1/2/3
Organism
hsa  Homo sapiens (human)
Pathway
hsa05034  Alcoholism
Drug target
Dilazep (DG00237): D02631<JP> D07843
Draflazine: D03906
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09160 Human Diseases
  09165 Substance dependence
   05034 Alcoholism
    2030 (SLC29A1)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    2030 (SLC29A1)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC29: Facilitative nucleoside transporter
   2030 (SLC29A1)
SSDB
Motif
Pfam: Nucleoside_tran
Other DBs
NCBI-GeneID: 2030
NCBI-ProteinID: NP_001071643
OMIM: 602193
HGNC: 11003
Ensembl: ENSG00000112759
Vega: OTTHUMG00000014759
Pharos: Q99808(Tclin)
UniProt: Q99808
Structure
PDB: 
6OB7 6OB6

Position
6p21.1
AA seq 456 aa
MTTSHQPQDRYKAVWLIFFMLGLGTLLPWNFFMTATQYFTNRLDMSQNVSLVTAELSKDA
QASAAPAAPLPERNSLSAIFNNVMTLCAMLPLLLFTYLNSFLHQRIPQSVRILGSLVAIL
LVFLITAILVKVQLDALPFFVITMIKIVLINSFGAILQGSLFGLAGLLPASYTAPIMSGQ
GLAGFFASVAMICAIASGSELSESAFGYFITACAVIILTIICYLGLPRLEFYRYYQQLKL
EGPGEQETKLDLISKGEEPRAGKEESGVSVSNSQPTNESHSIKAILKNISVLAFSVCFIF
TITIGMFPAVTVEVKSSIAGSSTWERYFIPVSCFLTFNIFDWLGRSLTAVFMWPGKDSRW
LPSLVLARLVFVPLLLLCNIKPRRYLTVVFEHDAWFIFFMAAFAFSNGYLASLCMCFGPK
KVKPAEAETAGAIMAFFLCLGLALGAVFSFLFRAIV
NT seq 1371 nt   +upstreamnt  +downstreamnt
atgacaaccagtcaccagcctcaggacagatacaaagctgtctggcttatcttcttcatg
ctgggtctgggaacgctgctcccgtggaattttttcatgacggccactcagtatttcaca
aaccgcctggacatgtcccagaatgtgtccttggtcactgctgaactgagcaaggacgcc
caggcgtcagccgcccctgcagcacccttgcctgagcggaactctctcagtgccatcttc
aacaatgtcatgaccctatgtgccatgctgcccctgctgttattcacctacctcaactcc
ttcctgcatcagaggatcccccagtccgtacggatcctgggcagcctggtggccatcctg
ctggtgtttctgatcactgccatcctggtgaaggtgcagctggatgctctgcccttcttt
gtcatcaccatgatcaagatcgtgctcattaattcatttggtgccatcctgcagggcagc
ctgtttggtctggctggccttctgcctgccagctacacggcccccatcatgagtggccag
ggcctagcaggcttctttgcctccgtggccatgatctgcgctattgccagtggctcggag
ctatcagaaagtgccttcggctactttatcacagcctgtgctgttatcattttgaccatc
atctgttacctgggcctgccccgcctggaattctaccgctactaccagcagctcaagctt
gaaggacccggggagcaggagaccaagttggacctcattagcaaaggagaggagccaaga
gcaggcaaagaggaatctggagtttcagtctccaactctcagcccaccaatgaaagccac
tctatcaaagccatcctgaaaaatatctcagtcctggctttctctgtctgcttcatcttc
actatcaccattgggatgtttccagccgtgactgttgaggtcaagtccagcatcgcaggc
agcagcacctgggaacgttacttcattcctgtgtcctgtttcttgactttcaatatcttt
gactggttgggccggagcctcacagctgtattcatgtggcctgggaaggacagccgctgg
ctgccaagcctggtgctggcccggctggtgtttgtgccactgctgctgctgtgcaacatt
aagccccgccgctacctgactgtggtcttcgagcacgatgcctggttcatcttcttcatg
gctgcctttgccttctccaacggctacctcgccagcctctgcatgtgcttcgggcccaag
aaagtgaagccagctgaggcagagaccgcaggagccatcatggccttcttcctgtgtctg
ggtctggcactgggggctgttttctccttcctgttccgggcaattgtgtga

KEGG   Homo sapiens (human): 3177
Entry
3177              CDS       T01001                                 

Gene name
SLC29A2, DER12, ENT2, HNP36
Definition
(RefSeq) solute carrier family 29 member 2
  KO
K15014  solute carrier family 29 (equilibrative nucleoside transporter), member 1/2/3
Organism
hsa  Homo sapiens (human)
Pathway
hsa05034  Alcoholism
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09160 Human Diseases
  09165 Substance dependence
   05034 Alcoholism
    3177 (SLC29A2)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    3177 (SLC29A2)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC29: Facilitative nucleoside transporter
   3177 (SLC29A2)
SSDB
Motif
Pfam: Nucleoside_tran
Other DBs
NCBI-GeneID: 3177
NCBI-ProteinID: NP_001287797
OMIM: 602110
HGNC: 11004
Ensembl: ENSG00000174669
Vega: OTTHUMG00000169056
Pharos: Q14542(Tbio)
UniProt: Q14542
Position
11q13.2
AA seq 456 aa
MARGDAPRDSYHLVGISFFILGLGTLLPWNFFITAIPYFQARLAGAGNSTARILSTNHTG
PEDAFNFNNWVTLLSQLPLLLFTLLNSFLYQCVPETVRILGSLLAILLLFALTAALVKVD
MSPGPFFSITMASVCFINSFSAVLQGSLFGQLGTMPSTYSTLFLSGQGLAGIFAALAMLL
SMASGVDAETSALGYFITPCVGILMSIVCYLSLPHLKFARYYLANKSSQAQAQELETKAE
LLQSDENGIPSSPQKVALTLDLDLEKEPESEPDEPQKPGKPSVFTVFQKIWLTALCLVLV
FTVTLSVFPAITAMVTSSTSPGKWSQFFNPICCFLLFNIMDWLGRSLTSYFLWPDEDSRL
LPLLVCLRFLFVPLFMLCHVPQRSRLPILFPQDAYFITFMLLFAVSNGYLVSLTMCLAPR
QVLPHEREVAGALMTFFLALGLSCGASLSFLFKALL
NT seq 1371 nt   +upstreamnt  +downstreamnt
atggcgcgaggagacgccccgcgggacagctaccacctggtcgggatcagcttcttcatc
ctggggctgggcaccctccttccctggaacttcttcatcaccgccatcccgtacttccag
gcgcgactggccggggccggcaacagcacagccaggatcctgagcaccaaccacacgggt
cccgaggatgccttcaacttcaacaattgggtgacgctgctgtcccagctgcccctgctg
ctcttcaccctcctcaactccttcctgtaccagtgcgtcccggagacggtgcgcattctg
ggcagcctgctggccatactgctgctctttgccctgacagcagcgctggtcaaggtggac
atgagccccggacccttcttctccatcaccatggcctccgtctgcttcatcaactccttc
agtgcagtcctacagggcagcctcttcgggcagctgggcaccatgccctccacctacagc
accctcttcctcagcggccagggcctggctgggatctttgctgcccttgccatgctcctg
tccatggccagtggcgtggacgccgagacctctgccctggggtactttatcacgccctgt
gtgggcatcctcatgtccatcgtgtgttacctgagcctgcctcacctgaagtttgcccgc
tactacctggccaataaatcatcccaggcccaagctcaggagctggagaccaaagctgag
ctcctccagtctgatgagaacgggattcccagtagtccccagaaagtagctctgaccctg
gatcttgacctggagaaggagccggaatcagagccagatgagccccagaagccaggaaaa
ccttcagtcttcactgtcttccagaagatctggctgacagcgctgtgccttgtgttggtc
ttcacagtcaccctgtccgtcttccccgccatcacagccatggtgaccagctccaccagt
cctgggaagtggagtcagttcttcaaccccatctgctgcttcctcctcttcaacatcatg
gactggctgggacggagcctgacctcttacttcctgtggccagacgaggacagccggctg
ctgcccctgctggtctgcctgcggttcctgttcgtgcccctcttcatgctgtgccacgtg
ccccagaggtcccggctgcccatcctcttcccacaggatgcctacttcatcaccttcatg
ctgctctttgccgtttctaatggctacctggtgtccctcaccatgtgcctggcgcccagg
caggtgctgccacacgagagggaggtggccggcgccctcatgaccttcttcctggccctg
ggactttcctgtggagcctccctctccttcctcttcaaggcgctgctctga

KEGG   Homo sapiens (human): 55315
Entry
55315             CDS       T01001                                 

Gene name
SLC29A3, ENT3, HCLAP, HJCD, PHID
Definition
(RefSeq) solute carrier family 29 member 3
  KO
K15014  solute carrier family 29 (equilibrative nucleoside transporter), member 1/2/3
Organism
hsa  Homo sapiens (human)
Pathway
hsa05034  Alcoholism
Disease
H00815  H syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09160 Human Diseases
  09165 Substance dependence
   05034 Alcoholism
    55315 (SLC29A3)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    55315 (SLC29A3)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC29: Facilitative nucleoside transporter
   55315 (SLC29A3)
SSDB
Motif
Pfam: Nucleoside_tran
Other DBs
NCBI-GeneID: 55315
NCBI-ProteinID: NP_060814
OMIM: 612373
HGNC: 23096
Ensembl: ENSG00000198246
Vega: OTTHUMG00000018424
Pharos: Q9BZD2(Tbio)
UniProt: Q9BZD2
Position
10q22.1
AA seq 475 aa
MAVVSEDDFQHSSNSTYRTTSSSLRADQEALLEKLLDRPPPGLQRPEDRFCGTYIIFFSL
GIGSLLPWNFFITAKEYWMFKLRNSSSPATGEDPEGSDILNYFESYLAVASTVPSMLCLV
ANFLLVNRVAVHIRVLASLTVILAIFMVITALVKVDTSSWTRGFFAVTIVCMVILSGAST
VFSSSIYGMTGSFPMRNSQALISGGAMGGTVSAVASLVDLAASSDVRNSALAFFLTATVF
LVLCMGLYLLLSRLEYARYYMRPVLAAHVFSGEEELPQDSLSAPSVASRFIDSHTPPLRP
ILKKTASLGFCVTYVFFITSLIYPAICTNIESLNKGSGSLWTTKFFIPLTTFLLYNFADL
CGRQLTAWIQVPGPNSKALPGFVLLRTCLIPLFVLCNYQPRVHLKTVVFQSDVYPALLSS
LLGLSNGYLSTLALLYGPKIVPRELAEATGVVMSFYVCLGLTLGSACSTLLVHLI
NT seq 1428 nt   +upstreamnt  +downstreamnt
atggccgttgtctcagaggacgactttcagcacagttcaaactccacctacagaaccaca
agcagcagtctccgagctgaccaggaggcactgcttgagaagctgctggaccgcccgccc
cctggcctgcagaggcccgaggaccgcttctgtggcacatacatcatcttcttcagcctg
ggcattggcagtctactgccatggaacttctttatcactgccaaggagtactggatgttc
aaactccgcaactcctccagcccagccaccggggaggaccctgagggctcagacatcctg
aactactttgagagctaccttgccgttgcctccaccgtgccctccatgctgtgcctggtg
gccaacttcctgcttgtcaacagggttgcagtccacatccgtgtcctggcctcactgacg
gtcatcctggccatcttcatggtgataactgcactggtgaaggtggacacttcctcctgg
acccgtggcttttttgcggtcaccattgtctgcatggtgatcctcagcggtgcctccact
gtcttcagcagcagcatctacggcatgaccggctcctttcctatgaggaactcccaggca
ctgatatcaggaggagccatgggcgggacggtcagcgccgtggcctcattggtggacttg
gctgcatccagtgatgtgaggaacagcgccctggccttcttcctgacggccactgtcttc
ctcgtgctctgcatgggactctacctgctgctgtccaggctggagtatgccaggtactac
atgaggcctgttcttgcggcccatgtgttttctggtgaagaggagcttccccaggactcc
ctcagtgccccttcggtggcctccagattcattgattcccacacaccccctctccgcccc
atcctgaagaagacggccagcctgggcttctgtgtcacctacgtcttcttcatcaccagc
ctcatctaccccgccatctgcaccaacatcgagtccctcaacaagggttcgggctcactg
tggaccaccaagtttttcatccccctcactaccttcctcctgtacaactttgctgaccta
tgtggccggcagctcaccgcctggatccaggtgccagggcccaatagcaaggcgctccca
gggttcgtgctcctccggacctgcctcatccccctcttcgtgctctgtaactaccagccc
cgcgtccacctgaagactgtggtcttccagtccgatgtgtaccccgcactcctcagctcc
ctgctggggctcagcaacggctacctcagcaccctggccctcctctacgggcctaagatt
gtgcccagggagctggctgaggccacgggagtggtgatgtccttttatgtgtgcttgggc
ttaacactgggctcagcctgctctaccctcctggtgcacctcatctag

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