Wnt9b | ENSMUSG00000018486 | NCBI 22412

Details for: Wnt9b

Gene ID: 22412

Symbol: Wnt9b

Ensembl ID: ENSMUSG00000018486

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

Associated with

Signaling by wnt
(R-MMU-195721)
Wnt ligand biogenesis and trafficking
(R-MMU-3238698)
Animal organ morphogenesis
(GO:0009887)
Branching involved in ureteric bud morphogenesis
(GO:0001658)
Branching morphogenesis of an epithelial tube
(GO:0048754)
Canonical wnt signaling pathway
(GO:0060070)
Cell-cell signaling
(GO:0007267)
Cell fate commitment
(GO:0045165)
Cellular response to starvation
(GO:0009267)
Co-receptor binding
(GO:0039706)
Collecting duct development
(GO:0072044)
Cytokine activity
(GO:0005125)
Embryonic cranial skeleton morphogenesis
(GO:0048701)
Establishment of planar polarity involved in nephron morphogenesis
(GO:0072046)
Extracellular region
(GO:0005576)
Extracellular space
(GO:0005615)
Frizzled binding
(GO:0005109)
In utero embryonic development
(GO:0001701)
Kidney development
(GO:0001822)
Kidney morphogenesis
(GO:0060993)
Kidney rudiment formation
(GO:0072003)
Male genitalia development
(GO:0030539)
Mesenchymal stem cell maintenance involved in nephron morphogenesis
(GO:0072038)
Mesonephric duct formation
(GO:0072181)
Mesonephric tubule development
(GO:0072164)
Metanephric tubule development
(GO:0072170)
Metanephric tubule formation
(GO:0072174)
Midbrain dopaminergic neuron differentiation
(GO:1904948)
Multicellular organism development
(GO:0007275)
Negative regulation of stem cell population maintenance
(GO:1902455)
Nephron tubule morphogenesis
(GO:0072078)
Neuron differentiation
(GO:0030182)
Non-canonical wnt signaling pathway
(GO:0035567)
Positive regulation of catalytic activity
(GO:0043085)
Receptor ligand activity
(GO:0048018)
Regulation of asymmetric cell division
(GO:0009786)
Regulation of mesenchymal to epithelial transition involved in metanephros morphogenesis
(GO:0003339)
Regulation of protein phosphorylation
(GO:0001932)
Regulation of tube size
(GO:0035150)
Roof of mouth development
(GO:0060021)
Signaling receptor binding
(GO:0005102)
Signal transduction
(GO:0007165)
Uterus morphogenesis
(GO:0061038)
Wnt-frizzled-lrp5/6 complex
(GO:1990851)
Wnt signaling pathway
(GO:0016055)
Wnt signaling pathway, planar cell polarity pathway
(GO:0060071)

Other Information

Proteins

Protein Wnt-9b
Q8C718_MOUSE

Genular Protein ID: 2693358388

Symbol: WNT9B_MOUSE

Name: Protein Wnt-9b

UniProtKB Accession Codes:

O35468 Q8VI90

Database IDs:

Citations:

PubMed ID: 11786923

Title: Molecular cloning and characterization of mouse Wnt14b, clustered with mouse Wnt3 in mouse chromosome 11.

PubMed ID: 11786923

PubMed ID: 12573259

Title: Mouse Wnt9b transforming activity, tissue-specific expression, and evolution.

PubMed ID: 12573259

DOI: 10.1016/s0888-7543(02)00012-5

PubMed ID: 9441749

Title: Isolation of two novel WNT genes, WNT14 and WNT15, one of which (WNT15) is closely linked to WNT3 on human chromosome 17q21.

PubMed ID: 9441749

DOI: 10.1006/geno.1997.5041

PubMed ID: 16054034

Title: Wnt9b plays a central role in the regulation of mesenchymal to epithelial transitions underlying organogenesis of the mammalian urogenital system.

PubMed ID: 16054034

DOI: 10.1016/j.devcel.2005.05.016

PubMed ID: 17537789

Title: Wnt/beta-catenin signaling regulates nephron induction during mouse kidney development.

PubMed ID: 17537789

DOI: 10.1242/dev.006155

PubMed ID: 22461561

Title: Wnt9b-dependent FGF signaling is crucial for outgrowth of the nasal and maxillary processes during upper jaw and lip development.

PubMed ID: 22461561

DOI: 10.1242/dev.075796

PubMed ID: 25257647

Title: Epigenetic mechanism causes Wnt9b deficiency and nonsyndromic cleft lip and palate in the A/WySn mouse strain.

PubMed ID: 25257647

DOI: 10.1002/bdra.23320

Sequence Information:

Length: 359
Mass: 38982
Checksum: C98D7B5F566B70F5
Sequence:

MRPAPALALA ALCLLVLPAA AAAAAYFGLT GREVLTPFPG LGTAAAPAQA GAHLKQCDLL 
KLSRRQKQLC RREPGLAETL RDAAHLGLLE CQFQFRQERW NCSLEGRTGL LQRGFKETAF 
LYAVSAAALT HALARACSAG RMERCTCDDS PGLESRQAWQ WGVCGDNLKY STKFLSNFLG 
PKRGSKDLRA RADAHNTHVG IKAVKSGLRT TCKCHGVSGS CAVRTCWKQL SPFRETGQVL 
KLRYDTAVKV SSATNEALGR LELWAPAKPG GPAKGLAPRP GDLVYMEDSP SFCRPSKYSP 
GTAGRVCSRD SSCSSLCCGR GYDTQSRMVV FSCHCQVQWC CYVECQQCAQ QELVYTCKR

Genular Protein ID: 619530523

Symbol: Q8C718_MOUSE

Name: N/A

UniProtKB Accession Codes:

Q8C718

Database IDs:

Citations:

PubMed ID: 10349636

Title: High-efficiency full-length cDNA cloning.

PubMed ID: 10349636

DOI: 10.1016/S0076-6879(99)03004-9

PubMed ID: 11042159

Title: Normalization and subtraction of cap-trapper-selected cDNAs to prepare full-length cDNA libraries for rapid discovery of new genes.

PubMed ID: 11042159

DOI: 10.1101/gr.145100

PubMed ID: 11076861

Title: RIKEN integrated sequence analysis (RISA) system--384-format sequencing pipeline with 384 multicapillary sequencer.

PubMed ID: 11076861

DOI: 10.1101/gr.152600

PubMed ID: 11217851

Title: Functional annotation of a full-length mouse cDNA collection.

PubMed ID: 11217851

DOI: 10.1038/35055500

PubMed ID: 12466851

Title: Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs.

PubMed ID: 12466851

DOI: 10.1038/nature01266

PubMed ID: 16141073

Title: Antisense Transcription in the Mammalian Transcriptome.

PubMed ID: 16141073

DOI: 10.1126/science.1112009

Sequence Information:

Length: 359
Mass: 38986
Checksum: 9D893B1B522F70F2
Sequence:

MRPAPALALA ALCLLVLPAA AAAAAYFGLT GREVLTPFPG LGTAAAPAQA GAHLKQCDLL 
KLSRRQKQLC RREPGLAETL RDAAHLGLLE CQFQFRQERW NCSLEGRTGL LQRGFKETAF 
LYAVSAAALT HALARACSAG RMERCTCDDS PGLESRQAWQ WGVCGDNLKY STKFLSNFLG 
PKRGSKDLRA RADAHNTHVG IKAVKSGLRT TCKCHGVSGS CAVRTCWKQL SPFRETGQVL 
KLRYDTAVKV SSATNEALGR LELWAPAKPG GTAKGLAPRP GDLVYMEDSP SFCRPSKYSP 
GTAGRVCSRD SSCSSLCCGR GYDTQSRMVV FSCHCQVQWC CYVECQQCAQ QELVYTCKR

The gene details are incomplete or unavailable at the moment.

Database document:

This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.

Details for: Wnt9b

Associated with

Other Information

Molecular cloning and characterization of mouse Wnt14b, clustered with mouse Wnt3 in mouse chromosome 11. PubMed ID: 11786923

Mouse Wnt9b transforming activity, tissue-specific expression, and evolution. PubMed ID: 12573259

Isolation of two novel WNT genes, WNT14 and WNT15, one of which (WNT15) is closely linked to WNT3 on human chromosome 17q21. PubMed ID: 9441749

Wnt9b plays a central role in the regulation of mesenchymal to epithelial transitions underlying organogenesis of the mammalian urogenital system. PubMed ID: 16054034

Wnt/beta-catenin signaling regulates nephron induction during mouse kidney development. PubMed ID: 17537789

Wnt9b-dependent FGF signaling is crucial for outgrowth of the nasal and maxillary processes during upper jaw and lip development. PubMed ID: 22461561

Epigenetic mechanism causes Wnt9b deficiency and nonsyndromic cleft lip and palate in the A/WySn mouse strain. PubMed ID: 25257647

High-efficiency full-length cDNA cloning. PubMed ID: 10349636

Normalization and subtraction of cap-trapper-selected cDNAs to prepare full-length cDNA libraries for rapid discovery of new genes. PubMed ID: 11042159

RIKEN integrated sequence analysis (RISA) system--384-format sequencing pipeline with 384 multicapillary sequencer. PubMed ID: 11076861

Functional annotation of a full-length mouse cDNA collection. PubMed ID: 11217851

Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs. PubMed ID: 12466851

Antisense Transcription in the Mammalian Transcriptome. PubMed ID: 16141073