SLX4 gene homepage

General information
Gene symbol SLX4
Gene name SLX4 structure-specific endonuclease subunit
Chromosome 16
Chromosomal band p13.3
Imprinted Unknown
Genomic reference LRG_503
Transcript reference NM_032444.2
Associated with diseases FANCP
Citation reference(s) -
Curators (1) Despoina Kalfakakou
Total number of public variants reported 464
Unique public DNA variants reported 157
Individuals with public variants 408
Hidden variants 0
Date created May 20, 2020
Date last updated June 29, 2020
Version SLX4:200629

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 23845
Entrez Gene 84464
PubMed articles SLX4
OMIM - Gene 613278
OMIM - Diseases FANCP (Fanconi anemia, complementation group P)


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000204 16 SLX4 structure-specific endonuclease subunit NM_032444.2 NP_115820.2 464


Copyright & disclaimer
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