Neogale vison (American mink): 122915799 Help Entry 122915799         CDS       T08764                                  Symbol POMC Name (RefSeq) pro-opiomelanocortin   KO K05228   proopiomelanocortin Organism nvs  Neogale vison (American mink) Pathway nvs04024   cAMP signaling pathway nvs04080   Neuroactive ligand-receptor interaction nvs04081   Hormone signaling nvs04082   Neuroactive ligand signaling nvs04915   Estrogen signaling pathway nvs04916   Melanogenesis nvs04920   Adipocytokine signaling pathway nvs04925   Aldosterone synthesis and secretion nvs04927   Cortisol synthesis and secretion nvs04934   Cushing syndrome Brite KEGG Orthology (KO) [BR:nvs00001]  09130 Environmental Information Processing   09132 Signal transduction    04024 cAMP signaling pathway     122915799 (POMC)   09133 Signaling molecules and interaction    04080 Neuroactive ligand-receptor interaction     122915799 (POMC)    04082 Neuroactive ligand signaling     122915799 (POMC)    04081 Hormone signaling     122915799 (POMC)  09150 Organismal Systems   09152 Endocrine system    04920 Adipocytokine signaling pathway     122915799 (POMC)    04915 Estrogen signaling pathway     122915799 (POMC)    04916 Melanogenesis     122915799 (POMC)    04925 Aldosterone synthesis and secretion     122915799 (POMC)    04927 Cortisol synthesis and secretion     122915799 (POMC)  09160 Human Diseases   09167 Endocrine and metabolic disease    04934 Cushing syndrome     122915799 (POMC)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04052 Cytokines and neuropeptides [BR:nvs04052]     122915799 (POMC) Cytokines and neuropeptides [BR:nvs04052]  Neuropeptides   GPCR binding    122915799 (POMC) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  ACTH_domain Op_neuropeptide NPP Motif Other DBs NCBI-GeneID:  122915799 NCBI-ProteinID:  XP_044118478 LinkDB All DBs Position 8:124834873..124838117 Genome browser AA seq 265 aa AA seqDB search MPRSCCSHPGALLLALLLQASVEVSGWCLESSQCQDLTTESNLLACIRACKPDLLAQTPV LPRSGDEPPLTENPRKYVMGHFRWDRFGPRNGSAGQKREEEEVAVGEGHALLPAGGRELR GDGSEPGPREGKRSYSMEHFRWGKPVGKKRRPVKVYPNGAEDESAEAFPLEFKRELAGER PEPALGPEGAAEGMAALADLEYGLVAEAEVAEKKDDGPYKMEHFRWGSPPKDKRYGGFMT SEKSQTPLVTLFKNAIIKNAHKKGQ NT seq 798 nt NT seq  +upstreamnt  +downstreamnt atgccgagatcgtgctgcagccacccaggggccctgctgttggccttgctgcttcaggcc tctgtggaagtgagtggctggtgcctggaaagcagccagtgtcaggacctcaccacggaa agtaacctgctggcgtgcatccgggcctgcaagcctgacctcctggcccagacgcctgtg ctcccccgcagcggcgacgagcccccgctgaccgagaacccgcggaagtatgtcatgggc cacttccgctgggaccggtttggcccccggaatggcagcgcgggccagaagcgcgaagaa gaggaggtcgccgtgggcgaaggccatgccctgctgcccgcgggcggccgggagctccgc ggcgatggcagcgagcccggcccccgcgagggcaagcgctcctattccatggagcacttc cgctggggcaagcctgtgggcaagaagcggcgcccggtgaaggtgtaccccaacggcgcc gaggacgagtcggccgaggccttcccgctcgagttcaagagagagctggccggggagcgg cctgagccggcgctcggccccgagggcgcggccgagggcatggcggccctggccgacctg gagtacggcctggtggcggaggccgaggtggcggagaagaaggacgacgggccctacaag atggagcacttccgctggggcagcccgcccaaggacaagcgctacggcggcttcatgacc tccgagaagagccagacccccctggtgacgctgttcaaaaacgccatcatcaagaacgcc cacaagaagggccagtga

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