Homo sapiens (human): 4159
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Entry
4159 CDS
T01001
Symbol
MC3R, BMIQ9, MC3, MC3-R, OB20, OQTL
Name
(RefSeq) melanocortin 3 receptor
KO
K04201
melanocortin 3 receptor
Organism
hsa
Homo sapiens (human)
Pathway
hsa04080
Neuroactive ligand-receptor interaction
Disease
H02106
Genetic obesity
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09133 Signaling molecules and interaction
04080 Neuroactive ligand-receptor interaction
4159 (MC3R)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04030 G protein-coupled receptors [BR:
hsa04030
]
4159 (MC3R)
G protein-coupled receptors [BR:
hsa04030
]
Rhodopsin family
Peptide
Melanocortin
4159 (MC3R)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
7tm_1
7tm_4
7TM_GPCR_Srsx
Motif
Other DBs
NCBI-GeneID:
4159
NCBI-ProteinID:
NP_063941
OMIM:
155540
HGNC:
6931
Ensembl:
ENSG00000124089
UniProt:
P41968
Structure
PDB
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All DBs
Position
20:56248732..56249815
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AA seq
323 aa
AA seq
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MNASCCLPSVQPTLPNGSEHLQAPFFSNQSSSAFCEQVFIKPEVFLSLGIVSLLENILVI
LAVVRNGNLHSPMYFFLCSLAVADMLVSVSNALETIMIAIVHSDYLTFEDQFIQHMDNIF
DSMICISLVASICNLLAIAVDRYVTIFYALRYHSIMTVRKALTLIVAIWVCCGVCGVVFI
VYSESKMVIVCLITMFFAMMLLMGTLYVHMFLFARLHVKRIAALPPADGVAPQQHSCMKG
AVTITILLGVFIFCWAPFFLHLVLIITCPTNPYCICYTAHFNTYLVLIMCNSVIDPLIYA
FRSLELRNTFREILCGCNGMNLG
NT seq
972 nt
NT seq
+upstream
nt +downstream
nt
atgaatgcttcgtgctgcctgccctctgttcagccaacactgcctaatggctcggagcac
ctccaagcccctttcttcagcaaccagagcagcagcgccttctgtgagcaggtcttcatc
aagcccgaggttttcctgtctctgggcatcgtcagtctgctggaaaacatcctggttatc
ctggccgtggtcaggaacggcaacctgcactccccgatgtacttctttctctgcagcctg
gcggtggccgacatgctggtaagtgtgtccaatgccctggagaccatcatgatcgccatc
gtccacagcgactacctgaccttcgaggaccagtttatccagcacatggacaacatcttc
gactccatgatctgcatctccctggtggcctccatctgcaacctcctggccatcgccgtc
gacaggtacgtcaccatcttttacgcgctccgctaccacagcatcatgaccgtgaggaag
gccctcaccttgatcgtggccatctgggtctgctgcggcgtctgtggcgtggtgttcatc
gtctactcggagagcaaaatggtcattgtgtgcctcatcaccatgttcttcgccatgatg
ctcctcatgggcaccctctacgtgcacatgttcctctttgcgcggctgcacgtcaagcgc
atagcagcactgccacctgccgacggggtggccccacagcaacactcatgcatgaagggg
gcagtcaccatcaccattctcctgggcgtgttcatcttctgctgggcccccttcttcctc
cacctggtcctcatcatcacctgccccaccaacccctactgcatctgctacactgcccac
ttcaacacctacctggtcctcatcatgtgcaactccgtcatcgacccactcatctacgct
ttccggagcctggaattgcgcaacacctttagggagattctctgtggctgcaacggcatg
aacttgggatag
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