Homo sapiens (human): 1908 Help Entry 1908              CDS       T01001                                  Gene name EDN3, ET-3, ET3, HSCR4, PPET3, WS4B Definition (RefSeq) endothelin 3   KO K05227   endothelin-3 Organism hsa  Homo sapiens (human) Pathway hsa04024   cAMP signaling pathway hsa04080   Neuroactive ligand-receptor interaction hsa04270   Vascular smooth muscle contraction hsa04924   Renin secretion Disease H00759   Waardenburg syndrome H00910   Hirschsprung disease H00916   Congenital central hypoventilation syndrome Brite KEGG Orthology (KO) [BR:hsa00001]  09130 Environmental Information Processing   09132 Signal transduction    04024 cAMP signaling pathway     1908 (EDN3)   09133 Signaling molecules and interaction    04080 Neuroactive ligand-receptor interaction     1908 (EDN3)  09150 Organismal Systems   09152 Endocrine system    04924 Renin secretion     1908 (EDN3)   09153 Circulatory system    04270 Vascular smooth muscle contraction     1908 (EDN3) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  Endothelin Motif Other DBs NCBI-GeneID:  1908 NCBI-ProteinID:  NP_996917 OMIM:  131242 HGNC:  3178 Ensembl:  ENSG00000124205 Vega:  OTTHUMG00000032867 Pharos:  P14138(Tbio) CPD:  C16013 UniProt:  P14138 LinkDB All DBs Structure PDB:  6IGK Thumbnails Position 20q13.32 AA seq 238 aa AA seqDB search MEPGLWLLFGLTVTSAAGFVPCSQSGDAGRRGVSQAPTAARSEGDCEETVAGPGEETVAG PGEGTVAPTALQGPSPGSPGQEQAAEGAPEHHRSRRCTCFTYKDKECVYYCHLDIIWINT PEQTVPYGLSNYRGSFRGKRSAGPLPGNLQLSHRPHLRCACVGRYDKACLHFCTQTLDVS SNSRTAEKTDKEEEGKVEVKDQQSKQALDLHHPKLMPGSGLALAPSTCPRCLFQEGAP NT seq 717 nt NT seq  +upstreamnt  +downstreamnt atggagccggggctgtggctccttttcgggctcacagtgacctccgccgcaggattcgtg ccttgctcccagtctggggatgctggcaggcgcggcgtgtcccaggcccccactgcagcc agatctgagggggactgtgaagagactgtggctggccctggcgaggagactgtggctggc cctggcgaggggactgtggccccgacagcactgcagggtccaagccctggaagccctggg caggagcaggcggccgagggggcccctgagcaccaccgatccaggcgctgcacgtgcttc acctacaaggacaaggagtgtgtctactattgccacctggacatcatttggatcaacact cccgaacagacggtgccctatggactgtccaactacagaggaagcttccggggcaagagg tctgcggggccacttccagggaatctgcagctctcacatcggccacacttgcgctgcgct tgtgtggggagatatgacaaggcctgcctgcacttttgcacccaaactctggacgtcagc agtaattcaaggacggcagaaaaaacagacaaagaagaggaagggaaggttgaagtcaag gaccaacaaagcaagcaggctttagacctccaccatccaaagctcatgcccggcagtgga ctcgccctcgctccatctacctgcccccgctgcctctttcaggaaggagccccttag

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