| Type | Description |
|---|---|
| Definition | dishevelled associated activator of morphogenesis 2 |
| Date | Results | Publications |
|---|---|---|
| 2021-01-16 16:00:00 | DAAM2 Variants Cause Nephrotic Syndrome via Actin Dysregulation. | 33232676 |
| 2018-06-09 10:39:00 | Biochemical analyses demonstrate that Daam2 associates with VHL and facilitates its ubiquitination and degradation. | 29053101 |
| 2017-03-25 10:54:00 | Reduction of Daam2 expression occurred with clinical improvement of the patients | 26293489 |
| 2014-08-09 12:24:00 | miR-335 regulates the expression of at least five formin family members, three of which are validated, FMNL3, FMN2 and DAAM2. | 24223803 |
| 2009-08-12 21:34:00 | Observational study of gene-disease association. (HuGE Navigator) | 19562778 |
| Type | IDs |
|---|---|
| Synonymous | dJ90A20A.1 |
| Gene |
UniProtKB-ID:
DAAM2_HUMAN,
A0A0J9YYF7_HUMAN
UniprotKB:
Q86T65,
A0A0J9YYF7
UniParc:
UPI000020DC88,
UPI0000231CFE,
UPI000016191D
EMBL:
AL592158,
AL590999,
AL161439,
AL136089,
CH471081,
AL357412,
AB002379,
FO393411,
AL833083
Ensembl:
ENSG00000146122
KO:
hsa:23500
|
| Nucleutide sequences |
EMBL-CDS:
CAI20010.2,
CAD89973.1,
EAX03996.1,
BAA20835.2,
EAX03995.1
Gene_ORFName:
hCG_33196
Ensembl_TRS:
ENST00000538976,
ENST00000398904,
ENST00000274867,
ENST00000633794
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000381876,
ENSP00000437808,
ENSP00000274867,
ENSP00000488831
RefSeq:
XP_006715103.3,
XP_016866119.1,
XP_006715106.1,
NP_001188356.1,
XP_006715105.1,
XP_006715102.3,
NP_056160.2,
XP_006715109.1,
XP_006715108.1
|
| Others |
UniRef100:
UniRef100_A0A0J9YYF7,
UniRef100_Q86T65
UniRef90:
UniRef90_Q86T65
UniRef50:
UniRef50_Q86T65
UniGene:
Hs.357128
CCDS:
CCDS54999.1,
CCDS56426.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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