Homo sapiens (human): 100151683
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Entry
100151683 ncRNA
T01001
Symbol
RNU4ATAC, LWS, MOPD1, RFMN, RNU4ATAC1, TALS, U4ATAC
Name
(RefSeq) RNA, U4atac small nuclear
KO
K26388
U4atac small nuclear RNA
Organism
hsa
Homo sapiens (human)
Disease
H00993
Microcephalic osteodysplastic primordial dwarfism, type I (MOPD I)
H01575
Roifman syndrome
H02871
Lowry-Wood syndrome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03041 Spliceosome [BR:
hsa03041
]
100151683 (RNU4ATAC)
09184 RNA family
03100 Non-coding RNAs [BR:
hsa03100
]
100151683 (RNU4ATAC)
Spliceosome [BR:
hsa03041
]
Splicing related RNAs
100151683 (RNU4ATAC)
Non-coding RNAs [BR:
hsa03100
]
Small nuclear RNA
Sm-class snRNA
100151683 (RNU4ATAC)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Other DBs
NCBI-GeneID:
100151683
OMIM:
601428
HGNC:
34016
Ensembl:
ENSG00000264229
LinkDB
All DBs
Position
2:121530880..121531009
Genome browser
NT seq
130 nt
NT seq
+upstream
nt +downstream
nt
aaccatccttttcttggggttgcgctactgtccaatgagcgcatagtgagggcagtactg
ctaacgcctgaacaacacacccgcatcaactagagcttttgctttattttggtgcaattt
ttggaaaaat
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