Overview

Variant ID 25621
Entrez Gene ID 987
Gene LRBA (GeneCards)
Location hg19 4:151675038-151675038
hg38 4:150753886-150753886
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000004.11:g.151675038 C>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 -0.1927
CADD Raw score (version 1.3) 0.420621 (Deleterious)
FATHMM raw prediction score 0.1048 (Tolerated)
Deleterious probability by DeFine 0.4298 (Neutral)
Entrez Gene ID 987 (NCBI Gene)
Official Gene Symbol LRBA (GeneCards)
Number of variants in LRBA in this database 6 (view all the variants)
Full name LPS responsive beige-like anchor protein
Band 4q31.3
Other IDs Vega: OTTHUMG00000161443
OMIM: 606453
HGNC: HGNC:1742
Ensembl: ENSG00000198589
Other names BGL, LBA, CDC4L, CVID8, LAB300
Summary The protein encoded by this gene is a member of the WDL-BEACH-WD (WBW) gene family. Its expression is induced in B cells and macrophages by bacterial lipopolysaccharides (LPS). The encoded protein associates with protein kinase A and may be involved in leading intracellular vesicles to activated receptor complexes, which aids in the secretion and/or membrane deposition of immune effector molecules. Defects in this gene are associated with the disorder common variable immunodeficiency-8 with autoimmunity. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2012]

Individual #1

Individual ID 29217587.02 (view all the variants in this individual)
Pubmed ID 29217587
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID