Homo sapiens (human): 26832
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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
Disease
H02459
Syndromic neurodevelopmental disorder
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)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Other DBs
NCBI-GeneID:
26832
OMIM:
621090
HGNC:
10212
Ensembl:
ENSG00000200156
LinkDB
All DBs
Position
15:65304677..65304793
Genome browser
NT seq
117 nt
NT seq
+upstream
nt +downstream
nt
atactctggtttctcttcagatcgtataaatctttcgccttttactaaagatttccgtgg
agaggaacaactctgagtcttaagctaattttttgaggccttgttccgacaaggcta
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