| Type | Description |
|---|---|
| Definition | stathmin 2 |
| Date | Results | Publications |
|---|---|---|
| 2021-02-20 13:36:00 | Truncated stathmin-2 is a marker of TDP-43 pathology in frontotemporal dementia. | 32790644 |
| 2020-03-07 11:08:00 | STMN2 is a key regulator functionally connected to known Parkinson's disease risk genes. Network analysis predicts a function of human STMN2 in synaptic trafficking. [Meta-Analysis} | 31748532 |
| 2019-05-25 11:28:00 | premature polyadenylation-mediated reduction in stathmin-2 is a hallmark of ALS-FTD that functionally links reduced nuclear TDP-43 function to enhanced neuronal vulnerability. | 30643298 |
| 2019-05-25 11:28:00 | expression of STMN2, which encodes a microtubule regulator, declined after TDP-43 knockdown and TDP-43 mislocalization as well as in patient-specific motor neurons and postmortem patient spinal cord. STMN2 loss upon reduced TDP-43 function was due to altered splicing, which is functionally important, as we show STMN2 is necessary for normal axonal outgrowth and regeneration. | 30643292 |
| 2014-12-06 12:15:00 | RARB and STMN2 polymorphisms were not associated with sporadic CJD in the Korean population. | 24414001 |
| Type | IDs |
|---|---|
| Synonymous | SCG10, SCGN10 |
| Gene |
UniProtKB-ID:
STMN2_HUMAN
UniprotKB:
Q93045
UniParc:
UPI0000E21B31,
UPI0000000C77
EMBL:
AC025599,
D50375,
S82024,
CR456833,
AC016240,
BQ069488,
CH471068,
BT020034,
AK292737,
BC006302
Ensembl:
ENSG00000104435
KO:
hsa:11075
|
| Nucleutide sequences |
EMBL-CDS:
AAH06302.1,
AAB36428.1,
BAF85426.1,
AAV38837.1,
CAG33114.1,
BAA23326.1,
EAW87065.1,
EAW87064.1
Ensembl_TRS:
ENST00000518111,
ENST00000220876
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000429243,
ENSP00000220876
RefSeq:
NP_001186143.1,
NP_008960.2,
XP_005251199.1
|
| Others |
UniRef100:
UniRef100_Q93045
UniRef90:
UniRef90_Q93045
UniRef50:
UniRef50_Q93045
UniGene:
Hs.521651
CCDS:
CCDS56542.1,
CCDS43748.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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