Homo sapiens (human): 84823 Help Entry 84823             CDS       T01001                                  Symbol LMNB2, EPM9, LAMB2, LMN2, MCPH27 Name (RefSeq) lamin B2   KO K07611   lamin B Organism hsa  Homo sapiens (human) Pathway hsa04210   Apoptosis hsa04820   Cytoskeleton in muscle cells Network nt06539  Cytoskeleton in muscle cells   Element N01822   Linker of nucleoskeleton and cytoskeleton (LINC) complex Disease H00269   Primary microcephaly H00420   Familial partial lipodystrophy H00810   Progressive myoclonic epilepsy Brite KEGG Orthology (KO) [BR:hsa00001]  09140 Cellular Processes   09143 Cell growth and death    04210 Apoptosis     84823 (LMNB2)   09142 Cell motility    04820 Cytoskeleton in muscle cells     84823 (LMNB2)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04812 Cytoskeleton proteins [BR:hsa04812]     84823 (LMNB2) Cytoskeleton proteins [BR:hsa04812]  Eukaryotic cytoskeleton proteins   Intermediate filaments    Intermediate filaments     Type V: Nuclear lamins      84823 (LMNB2) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Filament LTD BRE1 Atg11_middle Motif Other DBs NCBI-GeneID:  84823 NCBI-ProteinID:  NP_116126 OMIM:  150341 HGNC:  6638 Ensembl:  ENSG00000176619 UniProt:  Q03252 Structure PDBPDBj LinkDB All DBs Position 19:complement(2428166..2456959) Genome browser AA seq 620 aa AA seqDB search MSPPSPGRRREQRRPRAAATMATPLPGRAGGPATPLSPTRLSRLQEKEELRELNDRLAHY IDRVRALELENDRLLLKISEKEEVTTREVSGIKALYESELADARRVLDETARERARLQIE IGKLRAELDEVNKSAKKREGELTVAQGRVKDLESLFHRSEVELAAALSDKRGLESDVAEL RAQLAKAEDGHAVAKKQLEKETLMRVDLENRCQSLQEELDFRKSVFEEEVRETRRRHERR LVEVDSSRQQEYDFKMAQALEELRSQHDEQVRLYKLELEQTYQAKLDSAKLSSDQNDKAA SAAREELKEARMRLESLSYQLSGLQKQASAAEDRIRELEEAMAGERDKFRKMLDAKEQEM TEMRDVMQQQLAEYQELLDVKLALDMEINAYRKLLEGEEERLKLSPSPSSRVTVSRATSS SSGSLSATGRLGRSKRKRLEVEEPLGSGPSVLGTGTGGSGGFHLAQQASASGSVSIEEID LEGKFVQLKNNSDKDQSLGNWRIKRQVLEGEEIAYKFTPKYILRAGQMVTVWAAGAGVAH SPPSTLVWKGQSSWGTGESFRTVLVNADGEEVAMRTVKKSSVMRENENGEEEEEEAEFGE EDLFHQQGDPRTTSRGCYVM NT seq 1863 nt NT seq  +upstreamnt  +downstreamnt atgagcccgccgagcccgggccgccgtcgggagcagcgcaggccgcgagccgccgccacc atggccacgccgctgcccggccgcgcgggcgggcccgccacgccgctgtcgcccacgcgc ctgtcgcggctgcaggagaaggaggagctgcgcgagctcaacgaccgcctggcgcactac atcgaccgcgtccgcgcgctggagctggagaacgaccggctcctgctcaagatctcagag aaggaggaggtgaccacgcgcgaggtgagtggcatcaaggcgctgtacgagtcggagctg gccgatgcccggagagtcctggatgagacggctcgagagcgtgcccggctgcagatagag attgggaagctgagggcagagttggacgaggtcaacaagagcgccaagaagagggagggc gagcttacggtggcccagggccgtgtgaaggacctggagtccctgttccaccggagcgag gtggagctggcagctgccctcagcgacaagcgcggcctggagagtgacgtggctgagctg cgggcccagctggccaaggccgaggacggtcatgcagtggccaaaaagcagctggagaag gagacgctgatgcgtgtggacctggagaaccgctgccagagcctgcaggaggagctggac ttccggaagagtgtgttcgaggaggaggtgcgggagacgcggcggcggcacgagcggcgc ctggtggaggtggacagcagccggcagcaggagtacgacttcaagatggcacaggcgctg gaggagctgcggagccagcacgacgagcaagtgcggctctacaagctggagctggagcag acctaccaggccaagctggacagcgccaagctgagctctgaccagaacgacaaggcggcc agtgcggctcgcgaggagctgaaggaggcccgcatgcgcctggagtccctcagctaccag ctctccggcctccagaagcaggccagtgccgctgaagatcgcattcgggagctggaggag gccatggccggggagcgggacaagttccggaagatgctggacgccaaggagcaggagatg acggagatgcgggacgtgatgcagcagcagctggccgagtaccaggagctgctggacgtg aagctggccctggacatggagatcaacgcctaccggaagctcctggagggcgaggaggag aggctgaagctgtcccccagcccatcctcgcgcgtcaccgtctcacgagccacctcgagc agcagcggcagcttgtccgccaccgggcgcctgggccgcagtaagcggaagcggctggag gtggaggagcccttgggcagcggcccaagcgtcctgggcacgggcacgggtggcagcggt ggcttccacctggcccagcaggcctcggcctcgggtagcgtcagcatcgaggagatcgac ctggagggcaagtttgtgcagctcaagaacaactcggacaaggatcagtctctggggaac tggagaatcaagaggcaggtcttggagggggaggagatcgcctacaagttcacgcccaag tacatcctgcgcgccggccagatggtcacggtgtgggcagctggtgcgggggtggcccac agccccccctcgacgctggtgtggaagggccagagcagctggggcacgggcgagagcttc cgcaccgtcctggttaacgcggatggcgaggaagtggccatgaggactgtgaagaagtcc tcggtgatgcgtgagaatgagaatggggaggaagaggaggaggaagccgagtttggcgag gaggatcttttccaccaacagggggacccgaggaccacctcaagaggctgctacgtgatg tga

DBGET integrated database retrieval system