Hylobates moloch (silvery gibbon): 116810092
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Entry
116810092 CDS
T08803
Symbol
HTR2B
Name
(RefSeq) 5-hydroxytryptamine receptor 2B
KO
K04157
5-hydroxytryptamine receptor 2
Organism
hmh
Hylobates moloch (silvery gibbon)
Pathway
hmh04020
Calcium signaling pathway
hmh04080
Neuroactive ligand-receptor interaction
hmh04082
Neuroactive ligand signaling
hmh04540
Gap junction
hmh04726
Serotonergic synapse
hmh04750
Inflammatory mediator regulation of TRP channels
Brite
KEGG Orthology (KO) [BR:
hmh00001
]
09130 Environmental Information Processing
09132 Signal transduction
04020 Calcium signaling pathway
116810092 (HTR2B)
09133 Signaling molecules and interaction
04080 Neuroactive ligand-receptor interaction
116810092 (HTR2B)
04082 Neuroactive ligand signaling
116810092 (HTR2B)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04540 Gap junction
116810092 (HTR2B)
09150 Organismal Systems
09156 Nervous system
04726 Serotonergic synapse
116810092 (HTR2B)
09157 Sensory system
04750 Inflammatory mediator regulation of TRP channels
116810092 (HTR2B)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04030 G protein-coupled receptors [BR:
hmh04030
]
116810092 (HTR2B)
G protein-coupled receptors [BR:
hmh04030
]
Rhodopsin family
Biogenic amine
Serotonin
116810092 (HTR2B)
BRITE hierarchy
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Ortholog
Paralog
GFIT
Motif
Pfam:
7tm_1
7TM_GPCR_Srsx
7TM_GPCR_Srv
7tm_4
7TM_GPCR_Srx
Motif
Other DBs
NCBI-GeneID:
116810092
NCBI-ProteinID:
XP_058293390
LinkDB
All DBs
Position
Unknown
AA seq
481 aa
AA seq
DB search
MALSYRVSELQSTIPEHILQSTFVHVISSNWSGLQTESIPEEMKQIVEEQGNKLHWAALL
ILMVIIPTIGGNTLVILAVSLEKKLQYATNYFLMSLAVADLLVGLFVMPIALLTIMFEAT
WPLPLVLCPAWLFLDVLFSTASIMHLCAISVDRYIAIKKPIQANQYNSRATAFIKITVVW
LISIGIAIPVPIKGIETDVDNPNNITCVLTKERFGNFMLFGSLAAFFTPLAIMIVTYFLT
IHALQKKAYLVKNKPPQRLTWLTVSTVFQRDETPCSSPEKVAMLDGSRKDKALPNSGDET
VTRRTSTIGKKSVQTISNEQRASKVLGIVFFLFLLMWCPFFITNITLVLCDSCNQTTLQM
LLEIFVWIGYVSSGVNPLVYTLFNKTFRDAFGRYITCNYRATKSVKTLSKRSSKIYFRNP
MAENSKFFKKHGIRNGINPAMYQSPMRLRSSTIQSSSIILLDTLLLTENEGDKTEEQVSY
V
NT seq
1446 nt
NT seq
+upstream
nt +downstream
nt
atggctctctcttacagagtgtctgaacttcaaagcacaattcctgagcacattttgcag
agcacctttgttcacgttatctcttctaactggtctggattacagacagaatcaatacca
gaggaaatgaaacagattgttgaggaacagggaaataaactgcactgggcagctcttctg
atactcatggtgataatacccacaattggtggaaatactcttgttattctggctgtttcg
ctggagaaaaagctgcagtatgctactaattactttctaatgtccttggcggtggctgat
ctgctggttggattgtttgtgatgccaattgccctcttgacaataatgtttgaggctacg
tggcccctcccacttgttctatgtcctgcctggttatttcttgacgttctcttttcaacc
gcatccatcatgcatctctgtgccatttcagtggatcgttatatagccatcaaaaagcca
atccaggccaatcaatataactcacgggctacagcattcatcaagattacagtggtgtgg
ttaatttcaataggcattgccattccagtccctattaaagggatagagactgatgtggac
aacccaaacaatatcacttgtgtgctgacaaaggaacgttttggcaatttcatgctcttt
ggctcactggctgccttcttcacacctcttgcaattatgattgtcacctactttctcact
atccacgctttacagaagaaggcttacttggtcaaaaacaagccacctcaacgcctaaca
tggttgactgtgtctacagttttccaaagggatgaaacaccttgctcgtcaccggaaaag
gtggcaatgctggatggttctcgaaaggacaaggctctgcccaactcaggtgatgaaaca
gttacgcgaagaacatccacaattggaaaaaagtcagtgcagaccatttccaatgaacag
agagcctcaaaggtcctagggattgtgtttttcctctttttgcttatgtggtgtcccttc
tttattacaaatataactttagttttatgtgattcctgtaaccaaactactctccaaatg
ctcctggagatatttgtgtggataggctatgtttcctcaggagtgaatcctttggtctac
accctcttcaataagacatttcgggatgcgtttggccgatatatcacctgcaattaccgg
gccacaaagtcagtaaaaactcttagcaaacgctccagtaagatctacttccggaatcca
atggcagagaactctaagtttttcaagaaacatggtattcgaaatgggattaatcctgcc
atgtaccagagtccaatgaggctccgaagttcaaccattcagtcttcatcaatcattcta
ctagatacacttctcctcactgaaaatgaaggtgacaaaactgaagagcaagttagttat
gtatag
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