Type | Description |
---|---|
Definition | a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 20 |
Date | Results | Publications |
---|---|---|
2020-06-27 10:18:00 | Results provide compelling evidence that ADAMTS9 and ADAMTS20 were differentially sensitive to B3GLCT inactivation and suggest that the developmental defects in PTRPLS result from disruption of a subset of highly sensitive POFUT2/B3GLCT targets such as ADAMTS20. | 31600785 |
2019-04-13 10:39:00 | ADAMTS9 or ADAMTS20 mutagenesis impaired neural and yolk sac ciliogenesis, leading to morphogenetic anomalies resulting from impaired hedgehog signaling, which is transduced by primary cilia. | 30814516 |
2011-01-01 11:34:00 | These findings support a model in which cooperative versican proteolysis by ADAMTS9 in vascular endothelium and by ADAMTS20 in palate mesenchyme drives palatal shelf sculpting and extension. | 21041365 |
2010-01-21 00:00:00 | This protein is identified and characterized and its relation to other disintegrins and thrombospondin 1 repeats is examined. | 12562771 |
2010-01-21 00:00:00 | Adamts20 mutations in belted (bt) mice cause white spotting of the dorsal and ventral torso, indicative of defective neural crest (NC)-derived melanoblast development. | 18454205 |
Type | IDs |
---|---|
Synonymous | Adamst20, bt |
Gene |
UniProtKB-ID:
ATS20_MOUSE,
Q3UQW9_MOUSE
UniprotKB:
P59511,
Q3UQW9
UniParc:
UPI000019333A,
UPI00001E9D29,
UPI00005AC0E8
EMBL:
AY189815,
AC084384,
AC084382,
AY189816,
AJ512753,
AK142029
Ensembl:
ENSMUSG00000022449
KO:
mmu:223838
|
Nucleutide sequences |
EMBL-CDS:
AAO74896.1,
AAO74895.1,
CAD54808.3,
BAE24919.1
Ensembl_TRS:
ENSMUST00000155907,
ENSMUST00000035342
|
Protein sequencees |
Ensembl_PRO:
ENSMUSP00000036330,
ENSMUSP00000121696
RefSeq:
NP_803180.3,
NP_001158258.1,
XP_006520926.1,
XP_011243896.1,
NP_001158257.1,
XP_017172070.1
|
Others |
UniRef100:
UniRef100_P59511-2,
UniRef100_P59511
UniRef90:
UniRef90_P59511,
UniRef90_P59511-2
UniRef50:
UniRef50_P59511,
UniRef50_P59511-2
UniGene:
Mm.214132
CCDS:
CCDS27770.1,
CCDS49711.1
|
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