The WDR35 gene homepage

General information
Gene symbol WDR35
Gene name WD repeat domain 35
Chromosome 2
Chromosomal band p24.3
Imprinted Unknown
Genomic reference NG_021212.1
Transcript reference NM_001006657.1
Exon/intron information NM_001006657.1 exon/intron table
Associated with diseases CED, CED2, ID, SRTD, SRTD7
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Joanna Walczak-Sztulpa
Total number of public variants reported 126
Unique public DNA variants reported 83
Individuals with public variants 505
Hidden variants 12
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 WDR35:240226

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_001006657.1.
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 https://www.LOVD.nl/WDR35
External URL Sensenbrenner syndrome website
HGNC 29250
Entrez Gene 57539
PubMed articles WDR35
OMIM - Gene 613602
OMIM - Diseases CED2 (dysplasia, cranioectodermal, type 2 (CED-2))
SRTD7 (SRPS5)
HGMD WDR35
GeneCards WDR35
GeneTests WDR35
Orphanet WDR35


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00024301 2 transcript variant 1 NM_001006657.1 NP_001006658.1 126


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