Type | Description |
---|---|
Definition | wingless-type MMTV integration site family, member 9B |
Date | Results | Publications |
---|---|---|
2020-01-04 11:36:00 | Co-transfection of M15 cells with Fzd5 (but no other Fzd family member) further increased the WNT9b signal to 16.8-fold and siRNA knockdown of Fzd5 reduced the signal by 52% | 30978219 |
2017-05-06 12:12:00 | Data indicate that mutations in wingless-type MMTV integration site family, member 9B protein (WNT9B) were frequently associated with Mayer-Rokitansky-Kuster-Hauser syndrome (MRKHS). | 26610373 |
2015-06-27 12:00:00 | Epigenetic mechanism causes Wnt9b deficiency and nonsyndromic cleft lip and palate in the A/WySn mouse strain. | 25257647 |
2013-05-04 10:47:00 | Expression of Wnt9b in Six2-positive cells disrupts cell fate decisions in the kidney and the gastrointestinal tract. | 22912798 |
2012-10-20 10:20:00 | Epithelial Wnt7b and Wnt9b as possible ligands of Fzd1-mediated beta-catenin (Ctnnb1)-dependent (canonical) Wnt signaling in the undifferentiated ureteric mesenchyme | 22833126 |
Type | IDs |
---|---|
Synonymous | Wnt14b, Wnt15, clf, clf1, wnt-14b, wnt-15 |
Gene |
UniProtKB-ID:
WNT9B_MOUSE,
Q8C718_MOUSE,
Q2TBA6_MOUSE
UniprotKB:
O35468,
Q8C718,
Q2TBA6
UniParc:
UPI00000E9A80,
UPI000005D2DF
EMBL:
BC110482,
AB073819,
AF031169,
AK052708,
AF469004
Ensembl:
ENSMUSG00000018486
KO:
mmu:22412
|
Nucleutide sequences |
EMBL-CDS:
AAC39950.1,
AAL82385.1,
BAB83866.1,
BAC35109.1,
AAI10483.1
Ensembl_TRS:
ENSMUST00000018630
|
Protein sequencees |
Ensembl_PRO:
ENSMUSP00000018630
RefSeq:
NP_035849.3,
XP_030101791.1
|
Others |
UniRef100:
UniRef100_O35468,
UniRef100_Q8C718
UniRef90:
UniRef90_O35468
UniRef50:
UniRef50_O35468
UniGene:
Mm.215161
CCDS:
CCDS25522.1
|
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