Overview

Variant ID 10424
Entrez Gene ID 64764
Gene CREB3L2 (GeneCards)
Location hg19 7:137619293-137619293
hg38 7:137934547-137934547
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000007.13:g.137619293 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 159138663

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0.00003228
EIGEN score 0.237
CADD Raw score (version 1.3) 0.147356 (Deleterious)
FATHMM raw prediction score 0.154 (Tolerated)
Deleterious probability by DeFine 0.4051 (Neutral)
Entrez Gene ID 64764 (NCBI Gene)
Official Gene Symbol CREB3L2 (GeneCards)
Number of variants in CREB3L2 in this database 3 (view all the variants)
Full name cAMP responsive element binding protein 3 like 2
Band 7q33
Other IDs Vega: OTTHUMG00000155744
OMIM: 608834
HGNC: HGNC:23720
Ensembl: ENSG00000182158
Other names BBF2H7
Summary This gene encodes a member of the oasis bZIP transcription factor family. Members of this family can dimerize but form homodimers only. The encoded protein is a transcriptional activator. Translocations between this gene on chromosome 7 and the gene fused in sarcoma on chromosome 16 can be found in some tumors. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]

Individual #1

Individual ID 29217584.03 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

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;