Eulemur rufifrons (Bennett's brown lemur): 138378393
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Entry
138378393 CDS
T11398
Symbol
HTR2C
Name
(RefSeq) 5-hydroxytryptamine receptor 2C
KO
K04157
5-hydroxytryptamine receptor 2
Organism
eruf Eulemur rufifrons (Bennett's brown lemur)
Pathway
eruf04020
Calcium signaling pathway
eruf04080
Neuroactive ligand-receptor interaction
eruf04082
Neuroactive ligand signaling
eruf04540
Gap junction
eruf04726
Serotonergic synapse
eruf04750
Inflammatory mediator regulation of TRP channels
Brite
KEGG Orthology (KO) [BR:
eruf00001
]
09130 Environmental Information Processing
09132 Signal transduction
04020 Calcium signaling pathway
138378393 (HTR2C)
09133 Signaling molecules and interaction
04080 Neuroactive ligand-receptor interaction
138378393 (HTR2C)
04082 Neuroactive ligand signaling
138378393 (HTR2C)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04540 Gap junction
138378393 (HTR2C)
09150 Organismal Systems
09156 Nervous system
04726 Serotonergic synapse
138378393 (HTR2C)
09157 Sensory system
04750 Inflammatory mediator regulation of TRP channels
138378393 (HTR2C)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04030 G protein-coupled receptors [BR:
eruf04030
]
138378393 (HTR2C)
G protein-coupled receptors [BR:
eruf04030
]
Rhodopsin family
Biogenic amine
Serotonin
138378393 (HTR2C)
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
7tm_1
7TM_GPCR_Srsx
7tm_4
7TM_GPCR_Srv
7TM_GPCR_Srx
Pox_P21
UPF0182
Motif
Other DBs
NCBI-GeneID:
138378393
NCBI-ProteinID:
XP_069319844
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All DBs
Position
30:complement(56686526..56990997)
Genome browser
AA seq
459 aa
AA seq
DB search
MVNLRNAVHSFLVHLVGLLVWQCDISISPVAAIVTDIFNTSDGGRFKFPDGVQNWPAISI
VVIIIMTIGGNILVIMAVSMEKKLHNATNYFLMSLAIADMLVGLLVMPLSLLAILYDYVW
PLPRYLCPVWISLDVLFSTASIMHLCAISLDRYVAIRNPIEHSRFNSRTKAIMKIAIVWA
ISIGVSVPIPVIGLRDEDKVFVNNTTCVLNDPNFVLIGSFVAFFIPLTIMVITYCLTIHV
LRRQALMLLHGHTEEPPGLSLDFLKCCKRNTADEENSANPNQDQNAGRRRKKKEKRPRGT
MQAINNEKKASKVLGIVFFVFLVMWCPFFITNILSVLCGKACNQKLMEKLLNVFVWIGYV
CSGINPLVYTLFNKTYRRAFSNYLRCNYKPEKKPPVRQIPRVAATALSGRELNVNIYRHT
NEQVVKKASDNEPGIEMQVENLELPVNPSNVVSERISSV
NT seq
1380 nt
NT seq
+upstream
nt +downstream
nt
atggtgaacctgaggaacgcggtgcattcgttccttgtgcacctagttggcctattggtt
tggcaatgcgatatttctataagcccagtagcagctatagtaactgacattttcaatacc
tccgatggtggacgcttcaaattcccagacggggtacaaaactggccagcaatttcaatc
gtcgtaataataatcatgacaataggtggcaacattctcgtaatcatggcagtaagcatg
gaaaagaaactgcacaatgccaccaattacttcttaatgtccctagccattgctgatatg
ctggtgggactccttgtcatgccactgtctctgcttgcaatcctttatgattatgtctgg
ccactacctagatatttgtgccccgtctggatatctttggatgttttattttcaacagcg
tccatcatgcacctctgcgctatatcgctggatcggtatgtagcaatacgtaatcctatt
gagcatagccgtttcaattcgcggactaaggccatcatgaagattgctatcgtttgggca
atatctataggtgtgtcagttcctatccctgtgattggactgagggacgaagacaaggtg
ttcgtgaacaacacgacgtgcgtgctcaatgacccaaatttcgttcttattgggtccttc
gtagctttcttcataccgctgacgattatggtgatcacgtattgcctgacgatccacgtt
cttcgcagacaagctttgatgttactgcacggccacaccgaggaaccgcctggactgagc
ctggatttcctgaagtgctgcaagaggaacaccgctgacgaagagaactctgccaaccct
aaccaagatcagaacgcaggtcgccgaagaaagaagaaggagaaacgtccgaggggcacc
atgcaggctatcaacaatgagaagaaagcctcgaaagtacttggcattgttttctttgtg
tttctggtcatgtggtgcccgtttttcattaccaatattctgtcagttctttgtgggaag
gcctgtaaccaaaagctcatggaaaagcttctgaatgtgtttgtttggataggctatgtt
tgttcaggaattaatcctctggtgtacacgctcttcaacaaaacttaccgaagggctttc
tccaactacttgcgctgcaattataagcctgagaaaaagccacctgtcagacaaattcca
agagttgccgccactgctttgtccgggagggagcttaatgttaacatttatcggcatacc
aatgaacaggtggttaagaaagctagcgacaacgagcctggtatagagatgcaagttgag
aatttggagctcccagtaaatccctctaatgtggttagcgaaaggattagtagtgtgtga
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