Homo sapiens (human): 136
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Entry
136 CDS
T01001
Symbol
ADORA2B, ADORA2
Name
(RefSeq) adenosine A2b receptor
KO
K04267
adenosine receptor A2b
Organism
hsa
Homo sapiens (human)
Pathway
hsa04015
Rap1 signaling pathway
hsa04020
Calcium signaling pathway
hsa04080
Neuroactive ligand-receptor interaction
hsa04082
Neuroactive ligand signaling
hsa04270
Vascular smooth muscle contraction
hsa05034
Alcoholism
Drug target
Adenosine (
DG00243
):
D00045
<JP/US>
D02300
<JP>
D02769
D08646
D08647
Aminophylline (
DG01062
):
D00227
D05429
<JP>
D11630
<US>
Diprophylline:
D00691
<JP>
Enprofylline:
D04006
Etrumadenant:
D12369
Proxyphylline:
D01771
<JP>
Theophylline (
DG01061
):
D00371
<JP/US>
D01712
D06103
D06104
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04015 Rap1 signaling pathway
136 (ADORA2B)
09133 Signaling molecules and interaction
04080 Neuroactive ligand-receptor interaction
136 (ADORA2B)
04082 Neuroactive ligand signaling
136 (ADORA2B)
09160 Human Diseases
09165 Substance dependence
05034 Alcoholism
136 (ADORA2B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04030 G protein-coupled receptors [BR:
hsa04030
]
136 (ADORA2B)
G protein-coupled receptors [BR:
hsa04030
]
Rhodopsin family
Base and nucleoside
Adenosine
136 (ADORA2B)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
7tm_1
7TM_GPCR_Srsx
7tm_4
GPR_Gpa2_C
7TM_GPCR_Srx
7TM_GPCR_Sri
Motif
Other DBs
NCBI-GeneID:
136
NCBI-ProteinID:
NP_000667
OMIM:
600446
HGNC:
264
Ensembl:
ENSG00000170425
UniProt:
P29275
Structure
PDB
PDBj
LinkDB
All DBs
Position
17:15850362..15975746
Genome browser
AA seq
332 aa
AA seq
DB search
MLLETQDALYVALELVIAALSVAGNVLVCAAVGTANTLQTPTNYFLVSLAAADVAVGLFA
IPFAITISLGFCTDFYGCLFLACFVLVLTQSSIFSLLAVAVDRYLAICVPLRYKSLVTGT
RARGVIAVLWVLAFGIGLTPFLGWNSKDSATNNCTEPWDGTTNESCCLVKCLFENVVPMS
YMVYFNFFGCVLPPLLIMLVIYIKIFLVACRQLQRTELMDHSRTTLQREIHAAKSLAMIV
GIFALCWLPVHAVNCVTLFQPAQGKNKPKWAMNMAILLSHANSVVNPIVYAYRNRDFRYT
FHKIISRYLLCQADVKSGNGQAGVQPALGVGL
NT seq
999 nt
NT seq
+upstream
nt +downstream
nt
atgctgctggagacacaggacgcgctgtacgtggcgctggagctggtcatcgccgcgctt
tcggtggcgggcaacgtgctggtgtgcgccgcggtgggcacggcgaacactctgcagacg
cccaccaactacttcctggtgtccctggctgcggccgacgtggccgtggggctcttcgcc
atcccctttgccatcaccatcagcctgggcttctgcactgacttctacggctgcctcttc
ctcgcctgcttcgtgctggtgctcacgcagagctccatcttcagccttctggccgtggca
gtcgacagatacctggccatctgtgtcccgctcaggtataaaagtttggtcacggggacc
cgagcaagaggggtcattgctgtcctctgggtccttgcctttggcatcggattgactcca
ttcctggggtggaacagtaaagacagtgccaccaacaactgcacagaaccctgggatgga
accacgaatgaaagctgctgccttgtgaagtgtctctttgagaatgtggtccccatgagc
tacatggtatatttcaatttctttgggtgtgttctgcccccactgcttataatgctggtg
atctacattaagatcttcctggtggcctgcaggcagcttcagcgcactgagctgatggac
cactcgaggaccaccctccagcgggagatccatgcagccaagtcactggccatgattgtg
gggatttttgccctgtgctggttacctgtgcatgctgttaactgtgtcactcttttccag
ccagctcagggtaaaaataagcccaagtgggcaatgaatatggccattcttctgtcacat
gccaattcagttgtcaatcccattgtctatgcttaccggaaccgagacttccgctacact
tttcacaaaattatctccaggtatcttctctgccaagcagatgtcaagagtgggaatggt
caggctggggtacagcctgctctcggtgtgggcctatga
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