FR399856

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  • Summary
  • Sequence
  • Secondary Structure
Evidence Mapping [blat]
blat with identity=99, coverage=90 and no-repeat
Evidence Sequence Similarity [highly similar]
Almost same sequences with one mismatch or one gap
Summary
ID FR399856
Description C/D box guide small nucleolar RNA (snoRNA) SNORD113 / SNORD114
Accession AL132709
Sequence Ontology C_D_box_snoRNA
Organism
Homo sapiens human , man
Genome Mapping
human(hg18)           1 region chr14:100499144-100499220(+) 
Cross Reference
Rfam v8.1 RF00181
Gene Association / Sense Overlap / 3'UTR
human(hg18) NR_003199 (uc001yix.1 )
Gene Association / Transcription Neighbor / upstream
human(hg18) NR_003201 (uc001yiz.1 ), NR_003200 (uc001yiy.1 )
Sequence Similarity
highly similar FR335002   C/D box small nucleolar RNA (snoRNA) 14q(II-7) / SNORD114-7

MicroArray / Invitrogen Ncode Noncoding RNA Array / hg18
ProbeTarget TranscriptProbe Locus
IVGNh29251 UC001YIX  chr14:100499159-100499219(+) 

Reference
Identification of tandemly-repeated C/D snoRNA genes at the imprinted human 14q32 domain reminiscent of those at the Prader-Willi/Angelman syndrome region.
Cavaillé J.,Seitz H.,Paulsen M.,Ferguson-Smith AC. and Bachellerie JP.
Hum Mol Genet 11 (13), 1527-38 (2002)

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