Macaca mulatta (rhesus monkey): 708141
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Entry
708141 CDS
T01028
Symbol
HTR2C
Name
(RefSeq) 5-hydroxytryptamine receptor 2C isoform X1
KO
K04157
5-hydroxytryptamine receptor 2
Organism
mcc
Macaca mulatta (rhesus monkey)
Pathway
mcc04020
Calcium signaling pathway
mcc04080
Neuroactive ligand-receptor interaction
mcc04082
Neuroactive ligand signaling
mcc04540
Gap junction
mcc04726
Serotonergic synapse
mcc04750
Inflammatory mediator regulation of TRP channels
Brite
KEGG Orthology (KO) [BR:
mcc00001
]
09130 Environmental Information Processing
09132 Signal transduction
04020 Calcium signaling pathway
708141 (HTR2C)
09133 Signaling molecules and interaction
04080 Neuroactive ligand-receptor interaction
708141 (HTR2C)
04082 Neuroactive ligand signaling
708141 (HTR2C)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04540 Gap junction
708141 (HTR2C)
09150 Organismal Systems
09156 Nervous system
04726 Serotonergic synapse
708141 (HTR2C)
09157 Sensory system
04750 Inflammatory mediator regulation of TRP channels
708141 (HTR2C)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04030 G protein-coupled receptors [BR:
mcc04030
]
708141 (HTR2C)
G protein-coupled receptors [BR:
mcc04030
]
Rhodopsin family
Biogenic amine
Serotonin
708141 (HTR2C)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
7tm_1
7TM_GPCR_Srsx
7tm_4
7TM_GPCR_Srx
DUF1385
UPF0182
DUF2208
Pox_P21
Motif
Other DBs
NCBI-GeneID:
708141
NCBI-ProteinID:
XP_028697795
Ensembl:
ENSMMUG00000009607
UniProt:
F7A578
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All DBs
Position
X:111272387..111434981
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AA seq
458 aa
AA seq
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MVNLRNAVHSFLVHLIGLLVWQCDISVSPVAAIVTDIFNTSDGGRFKFPDGVQNWPALSI
VVIIIMTIGGNILVIMAVSMEKKLHNATNYFLMSLAIADMLVGLLVMPLSLLAILYDYVW
PLPRYLCPVWISLDVLFSTASIMHLCAISLDRYVAIRNPIEHSRFNSRTKAIMKIAIVWA
ISIGVSVPIPVIGLRDEDKVFVNNTTCVLNDPNFVLIGSFVAFFIPLTIMVITYCLTIYV
LRRQALMLLHGHTEEPPGLSLDFLKCCKRNTAEEENAANPNQDQNARRRRKKERRPRGTM
QAINNERKASKVLGIVFFVFLIMWCPFFITNILSVLCEKSCNQKLMEKLLNVFVWIGYVC
SGINPLVYTLFNKIYRRAFSNYLRCNYKVEKKPPVRQIPRVAATALSGRELNVNIYRHTN
EPVIKKASDNEPGIEMQAENLELPVNPSSVVSERISSV
NT seq
1377 nt
NT seq
+upstream
nt +downstream
nt
atggtgaacctgaggaacgcggtgcattcattccttgtgcacctaattggcctattggtt
tggcaatgcgatatttctgtcagcccagtagcagctatagtaactgacattttcaatacc
tccgatggtggacgcttcaaattcccagacggggtacaaaactggccagcactttcaatc
gtcgtaataataatcatgacaataggtggcaacatacttgtgatcatggcagtaagcatg
gaaaagaaactgcacaatgccaccaattacttcttaatgtccctagccattgctgatatg
ctagtgggactacttgtcatgcccctgtctctcctggcaatcctttatgattatgtctgg
ccactacctagatatttgtgccccgtctggatttctttagatgttttattttcaacagcg
tccatcatgcacctctgcgctatatcgctggatcggtatgtagcaatacgtaatcctatt
gagcatagccgtttcaattcgcggactaaggccatcatgaagattgctattgtttgggca
atttctataggtgtatcagttcctatccctgtgattggactgagggacgaagacaaggtg
ttcgtgaacaacacgacgtgcgtgctcaacgacccaaatttcgttcttattgggtccttc
gtagctttcttcataccgctgacgattatggtgattacctattgcctgacgatctacgtt
cttcgccgacaagctttgatgttactgcacggccacaccgaggaaccgcctggactaagt
ctggatttcctgaagtgctgcaagaggaatacggccgaggaagagaacgctgcaaaccct
aaccaagaccagaacgcacgccgaagaaggaagaaggagagacgtcctaggggcaccatg
caggctatcaacaatgaaagaaaagcttcgaaagtccttgggattgttttctttgtgttt
ctgatcatgtggtgcccatttttcattaccaatattctgtcggttctttgtgagaagtcc
tgtaaccaaaagctcatggaaaagcttctgaatgtgtttgtttggattggctatgtgtgt
tcaggaatcaatcctctggtgtatactctcttcaacaaaatttaccgaagggcattctcc
aactatttgcgctgcaattataaggtagagaaaaagcctcctgtcaggcaaattccaaga
gttgccgccactgctttgtcagggagggagcttaatgttaacatttatcggcataccaat
gaaccggtgatcaagaaagccagtgacaatgagcccggtatagagatgcaagctgagaat
ttagagttaccagtaaatccctccagtgtggttagcgaaaggattagtagtgtgtga
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