The UNC80 gene homepage

General information
Gene symbol UNC80
Gene name unc-80 homolog (C. elegans)
Chromosome 2
Chromosomal band q35
Imprinted Unknown
Genomic reference NC_000002.11
Transcript reference NM_032504.1
Exon/intron information NM_032504.1 exon/intron table
Associated with diseases IHPRF2
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 90
Unique public DNA variants reported 71
Individuals with public variants 23
Hidden variants 19
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created May 03, 2013
Date last updated February 26, 2024
Version UNC80:240226

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_032504.1.
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
Homepage URL http://www.LOVD.nl/UNC80
HGNC 26582
Entrez Gene 285175
PubMed articles UNC80
OMIM - Gene 612636
OMIM - Diseases IHPRF2 (hypotonia, infantile, with psychomotor retardation and characteristic facies, type 2 (IHPRF-2))
HGMD UNC80
GeneCards UNC80
GeneTests UNC80
Orphanet UNC80


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00024138 2 transcript variant 1 NM_032504.1 NP_115893.1 90


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