Tag | Content |
---|---|
UniProt Accession | BDNF_HUMAN; P23560; |
Entrez ID | 627 |
GenBank Protein ID | NM_001143805.1; NM_001143806.1; NM_001143807.1; NM_001143808.1; NM_001143809.1; NM_001143810.1; NM_001143811.1; NM_001143812.1; NM_001143813.1; NM_001143814.1; NM_001143816.1; NM_001709.4; NM_170731.4; NM_170732.4; NM_170733.3; NM_170734.3; NM_170735.5; XM_011520280.2; |
GenBank Nucleotide ID | NP_001137277.1; NP_001137278.1; NP_001137279.1; NP_001137280.1; NP_001137281.1; NP_001137282.1; NP_001137283.1; NP_001137284.1; NP_001137285.1; NP_001137286.1; NP_001137288.1; NP_001700.2; NP_733927.1; NP_733928.1; NP_733929.1; NP_733930.1; NP_733931.1; XP_011518582.1; |
Protein Name | Brain-derived neurotrophic factor (BDNF) (Abrineurin) |
Gene Name | BDNF |
Organism | Homo sapiens |
NCBI Taxa ID | 9606 |
Functional Description | During development, promotes the survival and differentiation of selected neuronal populations of the peripheral and central nervous systems. Participates in axonal growth, pathfinding and in the modulation of dendritic growth and morphology. Major regulator of synaptic transmission and plasticity at adult synapses in many regions of the CNS. The versatility of BDNF is emphasized by its contribution to a range of adaptive neuronal responses including long-term potentiation (LTP), long-term depression (LTD), certain forms of short-term synaptic plasticity, as well as homeostatic regulation of intrinsic neuronal excitability. |
Sequence (Fasta) | MTILFLTMVI SYFGCMKAAP MKEANIRGQG GLAYPGVRTH GTLESVNGPK AGSRGLTSLA 60 DTFEHVIEEL LDEDQKVRPN EENNKDADLY TSRVMLSSQV PLEPPLLFLL EEYKNYLDAA 120 NMSMRVRRHS DPARRGELSV CDSISEWVTA ADKKTAVDMS GGTVTVLEKV PVSKGQLKQY 180 FYETKCNPMG YTKEGCRGID KRHWNSQCRT TQSYVRALTM DSKKRIGWRF IRIDTSCVCT 240 LTIKRGR 248 |
|
Database | Annotation |
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CTD (Curated) (count: 33) (view all) | MESH:D000544
; Alzheimer Disease MESH:D019969 ; Amphetamine-Related Disorders MESH:D000067877 ; Autism Spectrum Disorder MESH:D001321 ; Autistic Disorder MESH:D001714 ; Bipolar Disorder MESH:D001835 ; Body Weight |
HGMD (count: 9) (view all) | CE068220; Bipolar disorder, susceptibility, association with; Repeat variations
CP068169; Bipolar disorder, association with; Complex rearrangements CP066519; Hyperphagia and severe obesity; Complex rearrangements CM023769; Central hypoventilation syndrome ?; Missense/nonsense CM020369; Parkinson disease, association with; Missense/nonsense CR014434; Alzheimer disease, association with; Regulatory |
GWASdb (count: 19) (view all) | rs6265; Weight; obesity
rs6265; Body mass index; obesity rs6265; Smoking behavior; nicotine dependence|lung cancer rs6265; Eating disorders; eating disorder rs11030101; Bone mineral density (paediatric, skull); bone resorption disease rs11030104; Body mass index; obesity |
PTM | Modification Sites |
---|---|
Phosphorylation (count: 6) | 11 LFLTMVISYFGCMKA dbPAF
12 FLTMVISYFGCMKAA dbPAF 155 VTAADKKTAVDMSGG dbPAF 191 TKCNPMGYTKEGCRG dbPAF 62 GLTSLADTFEHVIEE dbPAF 7 *MTILFLTMVISYFG dbPAF |
Network | Interaction | ||
---|---|---|---|
A | B | Source | |