Overview

Variant ID 18593
Entrez Gene ID 145581
Gene LRFN5 (GeneCards)
Location hg19 14:43380066-43380066
hg38 14:42910863-42910863
Disease Cockayne syndrome (view all the variants in this disease)
Method HiSeq X Ten
Mutation(HGVS format) NC_000014.8:g.43380066 G>A (Genome Assembly: GRCh37)

Other information

Exon or Intron NA
Position in protein NA
Amino acid changes in protein NA > NA
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 107349540

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.3291
CADD Raw score (version 1.3) 0.065602 (Deleterious)
FATHMM raw prediction score 0.08291 (Tolerated)
Deleterious probability by DeFine 0.0792 (Neutral)
Entrez Gene ID 145581 (NCBI Gene)
Official Gene Symbol LRFN5 (GeneCards)
Number of variants in LRFN5 in this database 36 (view all the variants)
Full name leucine rich repeat and fibronectin type III domain containing 5
Band 14q21.1
Other IDs Vega: OTTHUMG00000140261
OMIM: 612811
HGNC: HGNC:20360
Ensembl: ENSG00000165379
Other names SALM5, FIGLER8, C14orf146
Summary This gene encodes a protein that belongs to the leucine-rich repeat and fibronectin type III domain-containing family of proteins. A similar protein in mouse, a glycosylated transmembrane protein, is thought to function in presynaptic differentiation. [provided by RefSeq, Sep 2016]

Individual #1

Individual ID 29217584.16 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Female Patient  
Phenotype 3  
Disease Cockayne syndrome (view all the variants in this disease)
OMIM ID 216400

Publication #1: 29217584

Pubmed ID 29217584
Title Aging and neurodegeneration are associated with increased mutations in single human neurons.
Journal Science
Publication date 2018.02
Disease Cockayne syndrome Xeroderma Pigmentosum
Number of cases Male cases: 3; Female cases: 6; cases of unknown sex: 15;