WNT9B

Last updated
WNT9B
Identifiers
Aliases WNT9B , WNT14B, WNT15, Wnt family member 9B
External IDs OMIM: 602864 MGI: 1197020 HomoloGene: 2551 GeneCards: WNT9B
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_003396
NM_001320458

NM_011719

RefSeq (protein)

NP_001307387
NP_003387

NP_035849

Location (UCSC) Chr 17: 46.83 – 46.89 Mb Chr 11: 103.62 – 103.64 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Protein Wnt-9b (formerly Wnt15 [5] ) is a protein that in humans is encoded by the WNT9B gene. [6]

The Wnt family of genes produce glycolipoproteins that are involved with signaling and developmental processes. Like other Wnt genes, Wnt-9b codes for the Wnt-9b protein which participates in the canonical Wnt/β-catenin signaling pathway. Wnt-9b is a gene found on chromosome 17 in region 17q21. It can be traced to function in the establishment of the kidneys, because Wnt9 is critical for morphogenesis of the nephron. [7] This gene can impact kidney function in more than one way. Improper expression of the gene can cause cyst development on the kidney tubules, and in mice, mutant Wnt9 genes that cause lower protein concentrations resulted in failure of the kidneys to thrive shortly after birth. [8] Wnt-9b is a gene that often expressed in the epithelial cells of the Wolfian duct in early male and female embryos. In the embryos, Wnt11 is expressed at the branching points of the kidney tubules while Wnt-9b is expressed in a higher concentration at the stalk of the tubules. [9] Wnt-9b has also been tied to the involvement of neural differentiation by induction of retinoic acid, according to the NCBI. [10]

Related Research Articles

<span class="mw-page-title-main">Intermediate mesoderm</span> Layer of cells in mammalian embryos

Intermediate mesoderm or intermediate mesenchyme is a narrow section of the mesoderm located between the paraxial mesoderm and the lateral plate of the developing embryo. The intermediate mesoderm develops into vital parts of the urogenital system.

<span class="mw-page-title-main">ROR2</span> Protein

Tyrosine-protein kinase transmembrane receptor ROR2, also known as neurotrophic tyrosine kinase, receptor-related 2, is a protein that in humans is encoded by the ROR2 gene located on position 9 of the long arm of chromosome 9. This protein is responsible for aspects of bone and cartilage growth. It is involved in Robinow syndrome and autosomal dominant brachydactyly type B. ROR2 is a member of the receptor tyrosine kinase-like orphan receptor (ROR) family.

Prickle is also known as REST/NRSF-interacting LIM domain protein, which is a putative nuclear translocation receptor. Prickle is part of the non-canonical Wnt signaling pathway that establishes planar cell polarity. A gain or loss of function of Prickle1 causes defects in the convergent extension movements of gastrulation. In epithelial cells, Prickle2 establishes and maintains cell apical/basal polarity. Prickle1 plays an important role in the development of the nervous system by regulating the movement of nerve cells.

<span class="mw-page-title-main">WNT4</span> Protein-coding gene in the species Homo sapiens

WNT4 is a secreted protein that in humans is encoded by the WNT4 gene, found on chromosome 1. It promotes female sex development and represses male sex development. Loss of function can have serious consequences, such as female to male sex reversal.

<span class="mw-page-title-main">Notch 4</span> Protein-coding gene in the species Homo sapiens

Neurogenic locus notch homolog 4(Notch 4) is a protein that in humans is encoded by the NOTCH4 gene located on chromosome 6.

<span class="mw-page-title-main">Frizzled-2</span> Protein-coding gene in the species Homo sapiens

Frizzled-2(Fz-2) is a protein that in humans is encoded by the FZD2 gene.

<span class="mw-page-title-main">Frizzled-3</span> Protein-coding gene in the species Homo sapiens

Frizzled-3(Fz-3) is a protein that in humans is encoded by the FZD3 gene.

<span class="mw-page-title-main">DVL1</span> Human protein and coding gene

Segment polarity protein dishevelled homolog DVL-1 is a protein that in humans is encoded by the DVL1 gene.

<span class="mw-page-title-main">SCRIB</span> Protein-coding gene in the species Homo sapiens

SCRIB, also known as Scribble, SCRIBL, or Scribbled homolog (Drosophila), is a scaffold protein which in humans is encoded by the SCRIB gene. It was originally isolated in Drosophila melanogaster in a pathway (also known as the Scribble complex) with DLGAP5 (Discs large) and LLGL1 (Lethal giant larvae) as a tumor suppressor. In humans, SCRIB is found as a membrane protein and is involved in cell migration, cell polarity, and cell proliferation in epithelial cells. There is also strong evidence that SCRIB may play a role in cancer progression because of its strong homology to the Drosophila protein.

<span class="mw-page-title-main">WNT7A</span> Protein-coding gene in the species Homo sapiens

Protein Wnt-7a is a protein that in humans is encoded by the WNT7A gene.

<span class="mw-page-title-main">ZIC3</span> Protein-coding gene in the species Homo sapiens

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<span class="mw-page-title-main">WNT3</span> Protein and coding gene in humans

Proto-oncogene protein Wnt-3 is a protein that in humans is encoded by the WNT3 gene.

<span class="mw-page-title-main">WNT11</span> Protein-coding gene in the species Homo sapiens

Protein Wnt-11 is a protein that in humans is encoded by the WNT11 gene.

<span class="mw-page-title-main">WNT7B</span> Protein-coding gene in the species Homo sapiens

Wnt7b is a signaling protein that plays a crucial role for many developmental processes including placental, lung, eye, dendrite, and bone formation along with kidney development. The primary role of Wnt7b is to establish the cortico-medullary axis of epithelial organization.

<span class="mw-page-title-main">Planar cell polarity</span>

Planar cell polarity (PCP) is the protein-mediated signaling that coordinates the orientation of cells in a layer of epithelial tissue. In vertebrates, examples of mature PCP oriented tissue are the stereo-cilia bundles in the inner ear, motile cilia of the epithelium, and cell motility in epidermal wound healing. Additionally, PCP is known to be crucial to major developmental time points including coordinating convergent extension during gastrulation and coordinating cell behavior for neural tube closure. Cells orient themselves and their neighbors by establishing asymmetric expression of PCP components on opposing cell members within cells to establish and maintain the directionality of the cells. Some of these PCP components are transmembrane proteins which can proliferate the orientation signal to the surrounding cells.

<span class="mw-page-title-main">Forkhead box d1</span> Human protein-coding gene

Forkhead box D1 is a protein that in humans is encoded by the FOXD1 gene. Forkhead d1 is a kidney expressed transcription factor maps at the chromosome 5 at position 5q12—q13, identified in Drosophila forkhead protein and mammalian HNF3 transcription factor. The name of was derived from two spiked head structures in the embryos of Drosophila forkhead mutant. It belong to transcription factor family that displays remarkable functional diversity and involved in a wide variety of biological processes. The most commonly used synonyms for Forkhead D1 are, FOX D1, FREAC-4 and BF2.

<span class="mw-page-title-main">PRICKLE1</span> Protein-coding gene in the species Homo sapiens

Prickle planar cell polarity protein 1 is a protein that in humans is encoded by the PRICKLE1 gene.

<span class="mw-page-title-main">Madin-Darby canine kidney cells</span> Cell line

Madin-Darby canine kidney (MDCK) cells are a model mammalian cell line used in biomedical research. MDCK cells are used for a wide variety of cell biology studies including cell polarity, cell-cell adhesions, collective cell motility, toxicity studies, as well as responses to growth factors. It is one of few cell culture models that is suited for 3D cell culture and multicellular rearrangements known as branching morphogenesis.

<span class="mw-page-title-main">VANGL2</span> Protein-coding gene in the species Homo sapiens

VANGL planar cell polarity protein 2 is a protein that in humans is encoded by the VANGL2 gene.

Barry James Thompson is an Australian and British developmental biologist and cancer biologist. He is a professor of the John Curtin School of Medical Research at the Australian National University in Canberra. Thompson is known for identifying genes, proteins and mechanisms involved in epithelial polarity, morphogenesis and cell signaling via the Wnt and Hippo signaling pathways, which have key roles in human cancer.

References

  1. 1 2 3 ENSG00000276799 GRCh38: Ensembl release 89: ENSG00000158955, ENSG00000276799 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000018486 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Garriock RJ, Warkman AS, Meadows SM, D'Agostino S, Krieg PA (2007). "Census of vertebrate Wnt genes: isolation and developmental expression of Xenopus Wnt2, Wnt3, Wnt9a, Wnt9b, Wnt10a, and Wnt16". Developmental Dynamics. 236 (5): 1249–58. doi:10.1002/dvdy.21156. PMID   17436276. S2CID   21016668.
  6. "Entrez Gene: Wnt9b wingless-type MMTV integration site family, member 9B".
  7. Karner C, Chirumamilla R, Aoki S, et al. (2009). "Wnt9b signaling regulates planar cell polarity and kidney tubule morphogenesis". Nat Genet. 41 (7): 793–799. doi:10.1038/ng.400. PMC   2761080 . PMID   19543268.
  8. Karner C, Chirumamilla R, Aoki S, et al. (2009). "Wnt9b signaling regulates planar cell polarity and kidney tubule morphogenesis". Nat Genet. 41 (7): 793–799. doi:10.1038/ng.400. PMC   2761080 . PMID   19543268.
  9. Carroll T, Park J, Hayashi S, Majumdar A, McMahon A, et al. (2005). "Wnt9b Plays a Central Role in the Regulation of Mesenchymal to Epithelial Transitions Underlying Organogenesis of the Mammalian Urogenital System". Developmental Cell. 9 (2): 283–292. doi: 10.1016/j.devcel.2005.05.016 . PMID   16054034.
  10. "WNT9B Wnt family member 9B [Homo sapiens (human)]". NCBI Genes & Expression. 2021-04-06. Retrieved 2021-04-14.