Homo sapiens (human): 8996 Help Entry 8996              CDS       T01001                                  Symbol NOL3, ARC, FCM, MYOCL1, MYP, NOP, NOP30 Name (RefSeq) nucleolar protein 3   KO K28177   nucleolar protein 3 Organism hsa  Homo sapiens (human) Pathway hsa04210   Apoptosis Disease H02789   Familial myoclonus Brite KEGG Orthology (KO) [BR:hsa00001]  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     8996 (NOL3) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  CARD Trypan_PARP Motif Other DBs NCBI-GeneID:  8996 NCBI-ProteinID:  NP_001263236 OMIM:  605235 HGNC:  7869 Ensembl:  ENSG00000140939 UniProt:  O60936 Q5TZN6 Structure PDBPDBj LinkDB All DBs Position 16:67170538..67175737 Genome browser AA seq 208 aa AA seqDB search MGNAQERPSETIDRERKRLVETLQADSGLLLDALLARGVLTGPEYEALDALPDAERRVRR LLLLVQGKGEAACQELLRCAQRTAGAPDPAWDWQHVGPGYRDRSYDPPCPGHWTPEAPGS GTTCPGLPRASDPDEAGGPEGSEAVQSGTPEEPEPELEAEASKEAEPEPEPEPELEPEAE AEPEPELEPEPDPEPEPDFEERDESEDS NT seq 627 nt NT seq  +upstreamnt  +downstreamnt atgggcaacgcgcaggagcggccgtcagagactatcgaccgcgagcggaaacgcctggtc gagacgctgcaggcggactcgggactgctgttggacgcgctgctggcgcggggcgtgctc accgggccagagtacgaggcattggatgcactgcctgatgccgagcgcagggtgcgccgc ctactgctgctggtgcagggcaagggcgaggccgcctgccaggagctgctacgctgtgcc cagcgtaccgcgggcgcgccggaccccgcttgggactggcagcacgtgggtccgggctac cgggaccgcagctatgaccctccatgcccaggccactggacgccggaggcacccggctcg gggaccacatgccccgggttgcccagagcttcagaccctgacgaggccgggggccctgag ggctccgaggcggtgcaatccgggaccccggaggagccagagccagagctggaagctgag gcctctaaagaggctgaaccggagccggagccagagccagagctggaacccgaggctgaa gcagaaccagagccggaactggagccagaaccggacccagagcccgagcccgacttcgag gaaagggacgagtccgaagattcctga

DBGET integrated database retrieval system