The NOP56 gene homepage

General information
Gene symbol NOP56
Gene name NOP56 ribonucleoprotein
Chromosome 20
Chromosomal band p13
Imprinted Unknown
Genomic reference NG_032136.1
Transcript reference NM_006392.3
Associated with diseases SCA-36
Citation reference(s) -
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 24
Unique public DNA variants reported 23
Individuals with public variants 0
Hidden variants 0
Date created May 03, 2013
Date last updated September 15, 2020
Version NOP56:200915

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 15911
Entrez Gene 10528
PubMed articles NOP56
OMIM - Gene 614154
OMIM - Diseases SCA-36 (ataxia, spinocerebellar, type 36 (SCA-36))

Active transcripts




NCBI ID     

NCBI Protein ID     

00014690 20 NOP56 ribonucleoprotein homolog (yeast), transcript variant 1 NM_006392.3 NP_006383.2 24

Copyright & disclaimer
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