Homo sapiens (human): 267010
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Entry
267010 ncRNA
T01001
Symbol
RNU12, CDAGS, RNU12-1, RNU12L, RNU12P, SCAR33, dJ222E13.7
Name
(RefSeq) RNA, U12 small nuclear
Organism
hsa
Homo sapiens (human)
Disease
H01891
Autosomal recessive spinocerebellar ataxias
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NCBI-GeneID:
267010
OMIM:
620204
HGNC:
19380
Ensembl:
ENSG00000276027
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Position
22:42615244..42615393
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NT seq
150 nt
NT seq
+upstream
nt +downstream
nt
atgccttaaacttatgagtaaggaaaataacgattcggggtgacgcccgaatcctcactg
ctaatgtgagacgaatttttgagcgggtaaaggtcgccctcaaggtgacccgcctacttt
gcgggatgcctgggagttgcgatctgcccg
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