Pteropus alecto (black flying fox): 102887090
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Entry
102887090 CDS
T02993
Symbol
HTR2C
Name
(RefSeq) 5-hydroxytryptamine receptor 2C isoform X1
KO
K04157
5-hydroxytryptamine receptor 2
Organism
pale
Pteropus alecto (black flying fox)
Pathway
pale04020
Calcium signaling pathway
pale04080
Neuroactive ligand-receptor interaction
pale04082
Neuroactive ligand signaling
pale04540
Gap junction
pale04726
Serotonergic synapse
pale04750
Inflammatory mediator regulation of TRP channels
Brite
KEGG Orthology (KO) [BR:
pale00001
]
09130 Environmental Information Processing
09132 Signal transduction
04020 Calcium signaling pathway
102887090 (HTR2C)
09133 Signaling molecules and interaction
04080 Neuroactive ligand-receptor interaction
102887090 (HTR2C)
04082 Neuroactive ligand signaling
102887090 (HTR2C)
09140 Cellular Processes
09144 Cellular community - eukaryotes
04540 Gap junction
102887090 (HTR2C)
09150 Organismal Systems
09156 Nervous system
04726 Serotonergic synapse
102887090 (HTR2C)
09157 Sensory system
04750 Inflammatory mediator regulation of TRP channels
102887090 (HTR2C)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04030 G protein-coupled receptors [BR:
pale04030
]
102887090 (HTR2C)
G protein-coupled receptors [BR:
pale04030
]
Rhodopsin family
Biogenic amine
Serotonin
102887090 (HTR2C)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
7tm_1
7TM_GPCR_Srsx
7tm_4
7TM_GPCR_Srx
DUF1385
Pox_P21
UPF0182
Motif
Other DBs
NCBI-GeneID:
102887090
NCBI-ProteinID:
XP_006916232
LinkDB
All DBs
Position
Unknown
AA seq
456 aa
AA seq
DB search
MVNVRKVVHSFLVHLIGLLVWQCDISVSPVAAIVTDIFNTSDGGRFKFPDGVQNWPALSI
IIIIILTIGGNILVIMAVSLEKKLHNATNYFLMSLAIADMLVGLLVMPLSLLAILYDYVW
PLPRYLCPVWISLDVLFSTASIMHLCAISLDRYVAIRNPIEHSHFNSRTKAIMKIAIVWA
ISVGVSVPILVIGLRDEDKVFVSNTTCVLNDPNFVLIGSFVAFFIPLTIMVITYCLTIHV
LRRQALMLLHGHTEEPPGISLDFLKCCKKTTDENSVNPNQDLNPRGRKKKERRPRGTMQA
INNERKASKVLGIVFFVFLIMWCPFFITNILSVLCGKACNQKLMEKLLNVFVWIGYVCSG
INPLVYTLFNKVYRRAFSNYLRCNYKAEKKPPVRHMPRVAATVLSGRELNVNIYRHTNKP
VIKKAIDNEHEIEMQVENLELPVNPSNIVSERISNV
NT seq
1371 nt
NT seq
+upstream
nt +downstream
nt
atggtcaacgtgaggaaagtggtgcattcattcctcgtgcacctaattggcctattggtt
tggcaatgcgatatttctgtgagcccagttgcagctatagtaactgacattttcaatacc
tccgatggtggacgcttcaaattcccagacggggtacaaaactggccagcactttcaatc
atcataatcataatcttgacaataggtggcaacattctagttatcatggcagtaagcttg
gaaaagaaactacacaatgccaccaattacttcttaatgtccctagcaattgctgatatg
ctggtgggactacttgtcatgccactgtctctgcttgcaatcctttatgattatgtctgg
ccactacctagatatttgtgccccgtctggatttctttggatgttttattttctacggcg
tccatcatgcacctctgcgctatctcgctggatcggtatgtagcaatacgtaatcctatt
gagcatagccatttcaattcacggactaaggccatcatgaagattgctattgtttgggca
atttctgtaggcgtatcagttcctatcctagtgattggactgagagatgaagacaaagtg
tttgtcagtaacaccacctgcgtgctgaatgacccaaatttcgttcttattgggtccttc
gtagctttcttcataccgctgaccatcatggtgattacgtactgcctgacgatccacgtt
cttcgcagacaagctctgatgttactgcacggccacaccgaggaaccacccggaataagc
ctggatttcctgaagtgctgcaagaaaaccaccgatgaaaactctgtaaaccctaaccaa
gatttgaacccacgcggaagaaagaagaaagaaagacgtcctcggggcaccatgcaagct
atcaacaatgaacggaaagcatcgaaagtccttggcattgttttctttgtgtttctgatc
atgtggtgcccgttttttattaccaatattctgtcagttctttgtgggaaagcatgtaat
caaaagctcatggaaaaacttctgaatgtgtttgtttggattggctatgtttgttcagga
attaatcctctggtgtacactcttttcaacaaagtttaccgaagggctttttccaactac
ttgcgttgcaattataaggcagaaaaaaagcctcctgtcaggcatatgccaagagttgct
gccactgtgttgtctgggagggagctcaatgttaacatttaccggcacaccaataaacca
gtgataaagaaagctattgacaatgagcacgagatagagatgcaagttgagaatttggag
ctaccagtcaatccctccaatatagttagtgaaaggattagtaatgtgtaa
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