The DPY19L2 gene homepage

General information
Gene symbol DPY19L2
Gene name dpy-19-like 2 (C. elegans)
Chromosome 12
Chromosomal band q14.2
Imprinted Unknown
Genomic reference NG_031909.1
Transcript reference NM_173812.4
Exon/intron information NM_173812.4 exon/intron table
Associated with diseases INFM, SPGF, SPGF9
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 15
Unique public DNA variants reported 9
Individuals with public variants 5
Hidden variants 2
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was performed by Johan den Dunnen, supported by Global Variome.
Date created May 03, 2013
Date last updated April 09, 2022
Version DPY19L2:220409

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_173812.4.
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 https://www.LOVD.nl/DPY19L2
HGNC 19414
Entrez Gene 283417
PubMed articles DPY19L2
OMIM - Gene 613893
OMIM - Diseases SPGF9 (spermatogenic failure, type 9 (SPGF9))
HGMD DPY19L2
GeneCards DPY19L2
GeneTests DPY19L2
Orphanet DPY19L2


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00006671 12 dpy-19-like 2 (C. elegans) NM_173812.4 NP_776173.3 15


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