Variant ID | 10424 |
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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) |
Exon or Intron | NA |
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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 |
MAF in gnomAD genome (version 2.0.1) | 0.00003228 |
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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) |
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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 ID | 29217584.03 (view all the variants in this individual) |
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Pubmed ID | 29217584 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 29217584 |
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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; |