Overview

Variant ID 27031
Entrez Gene ID 4153
Gene MBL2 (GeneCards)
Location hg19 10:55048061-55048061
hg38 10:53288301-53288301
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000010.10:g.55048061 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 135534747

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.2779
CADD Raw score (version 1.3) 0.221633 (Deleterious)
FATHMM raw prediction score 0.066 (Tolerated)
Deleterious probability by DeFine 0.2734 (Neutral)
Entrez Gene ID 4153 (NCBI Gene)
Official Gene Symbol MBL2 (GeneCards)
Number of variants in MBL2 in this database 13 (view all the variants)
Full name mannose binding lectin 2
Band 10q21.1
Other IDs Vega: OTTHUMG00000150270
OMIM: 154545
HGNC: HGNC:6922
Ensembl: ENSG00000165471
Other names MBL, MBP, MBP1, MBPD, MBL2D, MBP-C, COLEC1, HSMBPC
Summary This gene encodes the soluble mannose-binding lectin or mannose-binding protein found in serum. The protein encoded belongs to the collectin family and is an important element in the innate immune system. The protein recognizes mannose and N-acetylglucosamine on many microorganisms, and is capable of activating the classical complement pathway. Deficiencies of this gene have been associated with susceptibility to autoimmune and infectious diseases. [provided by RefSeq, Jul 2008]

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