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22412 Wnt9b

22412

Wnt9b

wingless-type MMTV integration site family, member 9B

protein-coding

Mus musculus

基因描述

Type Description
Definition wingless-type MMTV integration site family, member 9B

研究结论

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

名称对应

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

全选

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