Overview

Variant ID 7119
Entrez Gene ID 254251
Gene LCORL (GeneCards)
Location hg19 4:18071337-18071337
hg38 4:18069714-18069714
Disease Cockayne syndrome (view all the variants in this disease)
Method HiSeq X Ten
Mutation(HGVS format) NC_000004.11:g.18071337 T>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 191154276

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.3094
CADD Raw score (version 1.3) -0.021075 (Deleterious)
FATHMM raw prediction score 0.10009 (Tolerated)
Deleterious probability by DeFine 0.225 (Neutral)
Entrez Gene ID 254251 (NCBI Gene)
Official Gene Symbol LCORL (GeneCards)
Number of variants in LCORL in this database 41 (view all the variants)
Full name ligand dependent nuclear receptor corepressor like
Band 4p15.31
Other IDs Vega: OTTHUMG00000128538
OMIM: 611799
HGNC: HGNC:30776
Ensembl: ENSG00000178177
Other names MLR1
Summary This gene encodes a transcription factor that appears to function in spermatogenesis. Polymorphisms in this gene are associated with measures of skeletal frame size and adult height. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]

Individual #1

Individual ID 29217584.17 (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;