FANCL gene homepage

General information
Gene symbol FANCL
Gene name FA complementation group L
Chromosome 2
Chromosomal band p16.1
Imprinted Unknown
Genomic reference LRG_501
Transcript reference NM_001114636.1, NM_018062.3
Associated with diseases FANCL
Citation reference(s) -
Curators (1) Despoina Kalfakakou
Total number of public variants reported 121
Unique public DNA variants reported 46
Individuals with public variants 152
Hidden variants 0
Date created May 20, 2020
Date last updated May 20, 2020
Version FANCL:200520

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 20748
Entrez Gene 55120
PubMed articles FANCL
OMIM - Gene 608111
OMIM - Diseases FANCL (Fanconi anemia, complementation group L)


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000083 2 Fanconi anemia, complementation group L, transcript variant 1 NM_001114636.1 NP_001108108.1 121
00000084 2 Fanconi anemia, complementation group L, transcript variant 2 NM_018062.3 NP_060532.2 121


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