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BDNF-AS (BDNF Antisense RNA) is an RNA Gene, and is affiliated with the lncRNA class. Diseases associated with BDNF-AS include Depression and Huntington Disease.
Name | Status | Disease Links | Group | Role | Mechanism of Action | Clinical Trials |
---|---|---|---|---|---|---|
antipsychotics | Pharma | 0 |
RNAcentral Transcript ID | Subcategory | Length (nts) | # of Sources | Source Identifiers and Annotations |
---|---|---|---|---|
URS0000361BAF_9606 | lncRNA | 596 | 4 |
Ensembl: ENST00000530313 (view in UCSC) , LncBook: HSALNT0173397, LNCipedia: BDNF-AS:19, NONCODE: NONHSAT018518.2, |
URS000075AB2C_9606 | lncRNA | 2036 | 3 |
RefSeq: NR_033312, Ensembl: ENST00000499568 (view in UCSC) , LncBook: HSALNT0173363, |
URS000075B01C_9606 | lncRNA | 1437 | 3 |
RefSeq: NR_033315, Ensembl: ENST00000500662 (view in UCSC) , LncBook: HSALNT0173354, |
URS000046132E_9606 | lncRNA | 572 | 3 |
Ensembl: ENST00000532965 (view in UCSC) , LncBook: HSALNT0173337, HSALNT0173338, NONCODE: NONHSAT018492.2, |
URS000075E443_9606 | lncRNA | 2320 | 2 |
RefSeq: NR_002832, Ensembl: ENST00000499008 (view in UCSC) , |
SNP ID | Clinical significance and condition | Chr 11 pos | Variation | AA Info | Type |
---|---|---|---|---|---|
981928 | Likely Pathogenic: Obesity | 27,658,008(+) |
C/T NM_001709.5(BDNF):c.557G>A (p.Cys186Tyr) |
MISSENSE | |
rs1287429853 | Uncertain Significance: not specified | 27,674,268(+) |
CTG/C NM_001709.5(BDNF):c.-21-15685_-21-15684del |
FRAMESHIFT_VARIANT,FIVE_PRIME_UTR_VARIANT,INTRON | |
rs138287649 | Likely Benign: not provided | 27,657,923(+) |
G/A NM_001709.5(BDNF):c.642C>T (p.Tyr214=) |
SYNONYMOUS | |
rs148736382 | Benign: not provided | 27,658,244(+) |
G/C NM_001709.5(BDNF):c.321C>G (p.Leu107=) |
NON_CODING_TRANSCRIPT_VARIANT,SYNONYMOUS | |
rs1554931219 | Likely Pathogenic: Inborn genetic diseases | 27,658,063(+) |
C/A NM_001709.5(BDNF):c.502G>T (p.Glu168Ter) |
NONSENSE |
Variant ID | Type | Subtype | PubMed ID |
---|---|---|---|
dgv135e201 | CNV | deletion | 23290073 |
dgv607n106 | CNV | deletion | 24896259 |
esv1476336 | CNV | insertion | 17803354 |
esv1745758 | CNV | deletion | 17803354 |
esv2064689 | CNV | deletion | 18987734 |
esv2672678 | CNV | deletion | 23128226 |
esv2744288 | CNV | deletion | 23290073 |
esv2744290 | CNV | deletion | 23290073 |
esv2744292 | CNV | deletion | 23290073 |
esv2744293 | CNV | deletion | 23290073 |
esv2744294 | CNV | deletion | 23290073 |
esv3258052 | CNV | deletion | 24192839 |
esv3357461 | CNV | insertion | 20981092 |
esv3454 | CNV | loss | 18987735 |
esv3547509 | CNV | deletion | 23714750 |
esv3625772 | CNV | loss | 21293372 |
esv3625773 | CNV | loss | 21293372 |
esv5866 | CNV | loss | 19470904 |
nsv1076609 | CNV | deletion | 25765185 |
nsv1141919 | OTHER | inversion | 24896259 |
nsv474533 | CNV | novel sequence insertion | 20440878 |
nsv819223 | CNV | gain | 19587683 |
nsv832095 | CNV | gain | 17160897 |
nsv957875 | CNV | insertion | 24416366 |
nsv958620 | CNV | deletion | 24416366 |
nsv971997 | CNV | duplication | 23825009 |
nsv982998 | CNV | duplication | 23825009 |
Disorder | Aliases | PubMed IDs |
---|---|---|
depression |
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huntington disease |
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retinoblastoma |
|
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body mass index quantitative trait locus 11 |
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schizophrenia |
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