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TCF4-AS1 (TCF4 Antisense RNA 1) is an RNA Gene, and is affiliated with the lncRNA class. Diseases associated with TCF4-AS1 include Pitt-Hopkins Syndrome.
RNAcentral Transcript ID | Subcategory | Length (nts) | # of Sources | Source Identifiers and Annotations |
---|---|---|---|---|
URS000036BB34_9606 | lncRNA | 396 | 3 |
Ensembl: ENST00000587660 (view in UCSC) , LNCipedia: TCF4-AS1:1, NONCODE: NONHSAT059369.2, |
URS00008E3A6A_9606 | lncRNA | 396 | 1 |
RefSeq: NR_132985, |
URS0001BCC7F8_9606 | lncRNA | 660 | 1 |
LncBook: HSALNT0251506, |
SNP ID | Clinical significance and condition | Chr 18 pos | Variation | AA Info | Type |
---|---|---|---|---|---|
833957 | Likely Benign: Pitt-Hopkins syndrome | 55,464,135(+) |
C/A NM_001083962.2(TCF4):c.148G>T (p.Val50Leu) |
MISSENSE | |
rs1341051748 | Uncertain Significance: Pitt-Hopkins syndrome | 55,464,140(+) |
A/C NM_001083962.2(TCF4):c.146-3T>G |
INTRON | |
rs143244149 | Benign/Likely Benign: Pitt-Hopkins syndrome; History of neurodevelopmental disorder; not specified | 55,461,054(+) |
T/C NM_001083962.2(TCF4):c.269A>G (p.Asn90Ser) |
MISSENSE | |
rs1555672050 | Uncertain Significance: Pitt-Hopkins syndrome | 55,464,101(+) |
T/C NM_001083962.2(TCF4):c.182A>G (p.Asn61Ser) |
MISSENSE | |
rs1568107383 | Likely Benign: Pitt-Hopkins syndrome | 55,461,033(+) |
T/C NM_001083962.2(TCF4):c.290A>G (p.Asn97Ser) |
MISSENSE |
Disorder | Aliases | PubMed IDs |
---|---|---|
pitt-hopkins syndrome |
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No publications were found for TCF4-AS1 Gene.