Homo sapiens (human): 26832 Help Entry 26832             ncRNA     T01001                                  Symbol RNU5B-1, RNU5B, RNU5B-1P, U5B1 Name (RefSeq) RNA, U5B small nuclear 1   KO K14279   U5 spliceosomal RNA Organism hsa  Homo sapiens (human) Pathway hsa03040   Spliceosome Network nt06547  Spliceosome   Element N01969   U4/U6-U5 snRNP fomation N01970   Spliceosome assembly (B complex formation) N01971   spliceosome activation N01972   Spliceosome catalysis (branching) N01993   Spliceosome catalysis (exon ligation) N01994   Spliceosome disassembly Disease H02997   Neurodevelopmental disorder with seizures and joint laxity Brite KEGG Orthology (KO) [BR:hsa00001]  09120 Genetic Information Processing   09121 Transcription    03040 Spliceosome     26832 (RNU5B-1)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03041 Spliceosome [BR:hsa03041]     26832 (RNU5B-1)   09184 RNA family    03100 Non-coding RNAs [BR:hsa03100]     26832 (RNU5B-1) Spliceosome [BR:hsa03041]  Splicing related RNAs   26832 (RNU5B-1) Non-coding RNAs [BR:hsa03100]  Small nuclear RNA   Sm-class snRNA    26832 (RNU5B-1) SSDB OrthologParalogGFIT Other DBs NCBI-GeneID:  26832 OMIM:  621090 HGNC:  10212 LinkDB All DBs Position 15:65304677..65304793 Genome browser NT seq 117 nt NT seq  +upstreamnt  +downstreamnt atactctggtttctcttcagatcgtataaatctttcgccttttactaaagatttccgtgg agaggaacaactctgagtcttaagctaattttttgaggccttgttccgacaaggcta

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