Free for academic non-profit institutions. Other users need a Commercial license
ATP1A1-AS1 (ATP1A1 Antisense RNA 1) is an RNA Gene, and is affiliated with the lncRNA class. Diseases associated with ATP1A1-AS1 include Charcot-Marie-Tooth Disease, Axonal, Type 2Dd and Hypomagnesemia, Seizures, And Mental Retardation 2.
RNAcentral Transcript ID | Subcategory | Length (nts) | # of Sources | Source Identifiers and Annotations |
---|---|---|---|---|
URS000075EE0D_9606 | lncRNA | 1828 | 4 |
RefSeq: NR_024125, LncBook: HSALNT0013238, LNCipedia: ATP1A1-AS1:3, NONCODE: NONHSAT005431.2, |
URS0000759F49_9606 | lncRNA | 1554 | 4 |
RefSeq: NR_024124, LncBook: HSALNT0013239, LNCipedia: ATP1A1-AS1:5, NONCODE: NONHSAT005430.2, |
URS000075E7C5_9606 | lncRNA | 671 | 4 |
RefSeq: NR_027645, LncBook: HSALNT0013234, LNCipedia: ATP1A1-AS1:4, NONCODE: NONHSAT005428.2, |
URS0000759969_9606 | lncRNA | 565 | 4 |
RefSeq: NR_027646, LncBook: HSALNT0013233, LNCipedia: ATP1A1-AS1:1, NONCODE: NONHSAT005424.2, |
URS00008B61B8_9606 | lncRNA | 1014 | 3 |
Ensembl: ENST00000369492 (view in UCSC) , LncBook: HSALNT0013243, LNCipedia: ATP1A1-AS1:6, |
SNP ID | Clinical significance and condition | Chr 01 pos | Variation | AA Info | Type |
---|---|---|---|---|---|
872433 | Likely Benign: not provided | 116,398,991(-) |
C/T NM_000701.8(ATP1A1):c.2355C>T (p.Pro785=) |
SYNONYMOUS | |
931627 | Uncertain Significance: Hypomagnesemia, seizures, and mental retardation 2 | 116,399,513(-) |
C/T NM_000701.8(ATP1A1):c.2542C>T (p.Arg848Trp) |
MISSENSE | |
992402 | Uncertain Significance: Hypomagnesemia, seizures, and mental retardation 2 | 116,396,627(-) |
C/G NM_000701.8(ATP1A1):c.1866C>G (p.Ile622Met) |
MISSENSE | |
995868 | Likely Pathogenic: Charcot-marie-tooth disease, axonal, type 2DD | 116,401,219(-) |
CTGTAAGACCAG/C NM_000701.8(ATP1A1):c.2809_2819del (p.Cys937fs) |
FRAMESHIFT | |
rs149820510 | Likely Benign: not provided | 116,399,512(-) |
G/A NM_000701.8(ATP1A1):c.2541G>A (p.Glu847=) |
SYNONYMOUS |
Disorder | Aliases | PubMed IDs |
---|---|---|
charcot-marie-tooth disease, axonal, type 2dd |
|
|
hypomagnesemia, seizures, and mental retardation 2 |
|
|
charcot-marie-tooth disease |
|
|