BDNF brain derived neurotrophic factor
Gene ID: 627, updated on 22-Apr-2024Gene type: protein coding
Also known as: ANON2; BULN2
- See all available tests in GTR for this gene
- Go to complete Gene record for BDNF
- Go to Variation Viewer for BDNF variants
Summary
This gene encodes a member of the nerve growth factor family of proteins. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature protein. Binding of this protein to its cognate receptor promotes neuronal survival in the adult brain. Expression of this gene is reduced in Alzheimer's, Parkinson's, and Huntington's disease patients. This gene may play a role in the regulation of the stress response and in the biology of mood disorders. [provided by RefSeq, Nov 2015]
Associated conditions
See all available tests in GTR for this gene
Description | Tests |
---|---|
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. GeneReviews: Not available | |
Common variants at CDKAL1 and KLF9 are associated with body mass index in east Asian populations. GeneReviews: Not available | |
Genome wide association study identifies KCNMA1 contributing to human obesity. GeneReviews: Not available | |
Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. GeneReviews: Not available | |
Genome-wide meta-analyses identify multiple loci associated with smoking behavior. GeneReviews: Not available | |
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. GeneReviews: Not available | |
Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption. GeneReviews: Not available | |
Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index. GeneReviews: Not available | |
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche. GeneReviews: Not available |
Genomic context
- Location:
- 11p14.1
- Sequence:
- Chromosome: 11; NC_000011.10 (27654893..27722030, complement)
- Total number of exons:
- 12
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for BDNF variants |
Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- BDNF database
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- RefSeqGeneLink to Nucleotide RefSeqGenes
- Variation ViewerRelated Variants
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