| Type | Description |
|---|---|
| Definition | VPS33A CORVET/HOPS core subunit |
| Date | Results | Publications |
|---|---|---|
| 2016-06-28 11:31:00 | VPS33A(D251E) mutation plays dual roles by increasing the HOPS complex assembly and its association with the autophagic SNARE complex, which selectively affects the autophagosome-lysosome fusion. | 26259518 |
| 2010-01-21 00:00:00 | VPS33A is mutated in Hermansky-Pudlak syndrome and may have a role in melanogenesis | 12538872 |
| 2010-01-21 00:00:00 | These studies suggest that loss of Purkinje neurons is the most obvious neurological atrophy in the buff mutant mouse, a structural change that generates motor coordination deficits and impaired postural phenotypes. | 19254700 |
| 2010-01-21 00:00:00 | Knockdown of Vps33a expression reduced the lysosomal storage of RANKL and caused the accumulation of newly synthesized RANKL in the Golgi apparatus, indicating that Vps33a is involved in transporting RANKL from the Golgi apparatus to secretory lysosomes. | 19419298 |
| Type | IDs |
|---|---|
| Synonymous | 3830421M04Rik, AI503300, AW048546, AW554476, bf |
| Gene |
UniProtKB-ID:
VP33A_MOUSE
UniprotKB:
Q9D2N9
UniParc:
UPI00000231DA
EMBL:
AK140553,
AK150282,
AK019463,
AF439858,
AK150550,
AK041982
Ensembl:
ENSMUSG00000029434
KO:
mmu:77573
|
| Nucleutide sequences |
EMBL-CDS:
BAB31735.1,
AAL33578.1,
BAE29438.1,
BAE29652.1,
BAC31121.1,
BAE24421.1
Ensembl_TRS:
ENSMUST00000031388
|
| Protein sequencees |
Ensembl_PRO:
ENSMUSP00000031388
RefSeq:
NP_001346442.1,
XP_006530567.1,
NP_084205.3
|
| Others |
UniRef100:
UniRef100_Q9D2N9
UniRef90:
UniRef90_Q9D2N9
UniRef50:
UniRef50_Q96AX1
UniGene:
Mm.41372
CCDS:
CCDS19666.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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