Type | Description |
---|---|
Definition | ataxin 3 |
Date | Results | Publications |
---|---|---|
2021-04-03 13:36:00 | Pathological ATX3 Expression Induces Cell Perturbations in E. coli as Revealed by Biochemical and Biophysical Investigations. | 33477953 |
2021-03-06 13:28:00 | RAN Translation of the Expanded CAG Repeats in the SCA3 Disease Context. | 33157084 |
2021-02-06 13:59:00 | CAG Repeat Size Influences the Progression Rate of Spinocerebellar Ataxia Type 3. | 32978817 |
2021-01-16 15:53:00 | Druggable genome screen identifies new regulators of the abundance and toxicity of ATXN3, the Spinocerebellar Ataxia type 3 disease protein. | 31783119 |
2021-01-09 13:34:00 | [Detection and analysis of dynamic variant in a pedigree affected with spinocerebellar ataxia type 3]. | 33306823 |
Type | IDs |
---|---|
Synonymous | AT3, ATX3, JOS, MJD, MJD1, SCA3 |
Gene |
UniProtKB-ID:
ATX3_HUMAN,
A0A0A0MS38_HUMAN,
C9JQV6_HUMAN
UniprotKB:
P54252,
A0A0A0MS38,
C9JQV6
UniParc:
UPI0001754A96,
UPI000013D23A,
UPI0001B7106B,
UPI00001694ED,
UPI0000140E20,
UPI0001B7106A,
UPI0001B71063
EMBL:
U64820,
U64822,
U64821,
AB038653,
AL121773,
AL049872,
AB050194,
S75313,
BC033711,
CH471061,
EU009923
Ensembl:
ENSG00000066427
KO:
hsa:4287
|
Nucleutide sequences |
EMBL-CDS:
AAB63354.1,
EAW81472.1,
AAH33711.1,
AAB33571.1,
BAB55646.1,
BAB55645.1,
AAB63352.1,
ABS29269.1,
AAB63353.1,
BAB18798.1
Ensembl_TRS:
ENST00000532032,
ENST00000503767,
ENST00000644486,
ENST00000340660,
ENST00000502250,
ENST00000393287,
ENST00000429774
|
Protein sequencees |
Ensembl_PRO:
ENSP00000426697,
ENSP00000437157,
ENSP00000339110,
ENSP00000496695,
ENSP00000425322,
ENSP00000376965,
ENSP00000389376
RefSeq:
NP_001158252.1,
NP_001158246.1,
NP_001158250.1,
NP_001158248.1,
NP_001121168.1,
NP_001158254.1,
NP_004984.2,
NP_001158249.1,
NP_001158251.1,
NP_001121169.2,
NP_001158253.1,
NP_109376.1
|
Others |
UniRef100:
UniRef100_A0A0A0MS38,
UniRef100_P54252,
UniRef100_C9JQV6
UniRef90:
UniRef90_C9JQV6,
UniRef90_P54252,
UniRef90_A0A0A0MS38
UniRef50:
UniRef50_P54252,
UniRef50_K7G901
UniGene:
Hs.532632
CCDS:
CCDS45154.1,
CCDS32143.1,
CCDS9900.1,
CCDS53908.1
|
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Refseq |
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