Homo sapiens (human): 5443
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Entry
5443 CDS
T01001
Symbol
POMC, ACTH, CLIP, LPH, MSH, NPP, OBAIRH, POC
Name
(RefSeq) proopiomelanocortin
KO
K05228
proopiomelanocortin
Organism
hsa
Homo sapiens (human)
Pathway
hsa04024
cAMP signaling pathway
hsa04080
Neuroactive ligand-receptor interaction
hsa04915
Estrogen signaling pathway
hsa04916
Melanogenesis
hsa04920
Adipocytokine signaling pathway
hsa04925
Aldosterone synthesis and secretion
hsa04927
Cortisol synthesis and secretion
hsa04934
Cushing syndrome
Network
nt06310
CRH-ACTH-cortisol signaling
nt06360
Cushing syndrome
Element
N00297
ACTH-cortisol signaling pathway
N00298
CYP11B1-CYP11B2 fusion to ACTH-cortisol signaling pathway
N00318
EGFR-ERK-ACTH signaling pathway
N00319
Mutation-activated USP8 to EGFR-ERK-ACTH signaling pathway
N00324
CRHR-PKA-ACTH signaling pathway
N00325
Mutation-inactivated RASD1 to CRHR-PKA-ACTH signaling pathway
N00326
Mutation-activated GNAS to CRHR-PKA-ACTH signaling pathway
N00327
Mutation-inactivated PRKAR1A to CRHR-PKA-ACTH signaling pathway
Disease
H02106
Genetic obesity
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04024 cAMP signaling pathway
5443 (POMC)
09133 Signaling molecules and interaction
04080 Neuroactive ligand-receptor interaction
5443 (POMC)
09150 Organismal Systems
09152 Endocrine system
04920 Adipocytokine signaling pathway
5443 (POMC)
04915 Estrogen signaling pathway
5443 (POMC)
04916 Melanogenesis
5443 (POMC)
04925 Aldosterone synthesis and secretion
5443 (POMC)
04927 Cortisol synthesis and secretion
5443 (POMC)
09160 Human Diseases
09167 Endocrine and metabolic disease
04934 Cushing syndrome
5443 (POMC)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04052 Cytokines and neuropeptides [BR:
hsa04052
]
5443 (POMC)
Cytokines and neuropeptides [BR:
hsa04052
]
Neuropeptides
Neuropeptides (GPCR binding)
5443 (POMC)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
ACTH_domain
NPP
Op_neuropeptide
Motif
Other DBs
NCBI-GeneID:
5443
NCBI-ProteinID:
NP_000930
OMIM:
176830
HGNC:
9201
Ensembl:
ENSG00000115138
CPD:
C16019
C16020
C02758
C02017
C02210
C16134
C16136
C16137
UniProt:
P01189
Structure
PDB
LinkDB
All DBs
Position
2:complement(25160860..25168580)
Genome browser
AA seq
267 aa
AA seq
DB search
MPRSCCSRSGALLLALLLQASMEVRGWCLESSQCQDLTTESNLLECIRACKPDLSAETPM
FPGNGDEQPLTENPRKYVMGHFRWDRFGRRNSSSSGSSGAGQKREDVSAGEDCGPLPEGG
PEPRSDGAKPGPREGKRSYSMEHFRWGKPVGKKRRPVKVYPNGAEDESAEAFPLEFKREL
TGQRLREGDGPDGPADDGAGAQADLEHSLLVAAEKKDEGPYRMEHFRWGSPPKDKRYGGF
MTSEKSQTPLVTLFKNAIIKNAYKKGE
NT seq
804 nt
NT seq
+upstream
nt +downstream
nt
atgccgagatcgtgctgcagccgctcgggggccctgttgctggccttgctgcttcaggcc
tccatggaagtgcgtggctggtgcctggagagcagccagtgtcaggacctcaccacggaa
agcaacctgctggagtgcatccgggcctgcaagcccgacctctcggccgagactcccatg
ttcccgggaaatggcgacgagcagcctctgaccgagaacccccggaagtacgtcatgggc
cacttccgctgggaccgattcggccgccgcaacagcagcagcagcggcagcagcggcgca
gggcagaagcgcgaggacgtctcagcgggcgaagactgcggcccgctgcctgagggcggc
cccgagccccgcagcgatggtgccaagccgggcccgcgcgagggcaagcgctcctactcc
atggagcacttccgctggggcaagccggtgggcaagaagcggcgcccagtgaaggtgtac
cctaacggcgccgaggacgagtcggccgaggccttccccctggagttcaagagggagctg
actggccagcgactccgggagggagatggccccgacggccctgccgatgacggcgcaggg
gcccaggccgacctggagcacagcctgctggtggcggccgagaagaaggacgagggcccc
tacaggatggagcacttccgctggggcagcccgcccaaggacaagcgctacggcggtttc
atgacctccgagaagagccagacgcccctggtgacgctgttcaaaaacgccatcatcaag
aacgcctacaagaagggcgagtga
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integrated database retrieval system