Identity
HGNC
LOCATION
17q21.32
LOCUSID
ALIAS
WNT14B,WNT15
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 7484
MIM: 602864
HGNC: 12779
Ensembl: ENSG00000158955
Variants:
dbSNP: 7484
ClinVar: 7484
TCGA: ENSG00000158955
COSMIC: WNT9B
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000158955 | ENST00000290015 | O14905 |
| ENSG00000158955 | ENST00000393461 | E7EPC3 |
| ENSG00000158955 | ENST00000575372 | I3L0L8 |
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 33704824 | 2021 | Genetic Variation in WNT9B Increases Relapse Hazard in Multiple Sclerosis. | 6 |
| 34145744 | 2021 | Homozygous WNT9B variants in two families with bilateral renal agenesis/hypoplasia/dysplasia. | 2 |
| 34324458 | 2021 | Wnt Family Member 9b (Wnt9b) Is a New Sensitive and Specific Marker for Breast Cancer. | 1 |
| 33704824 | 2021 | Genetic Variation in WNT9B Increases Relapse Hazard in Multiple Sclerosis. | 6 |
| 34145744 | 2021 | Homozygous WNT9B variants in two families with bilateral renal agenesis/hypoplasia/dysplasia. | 2 |
| 34324458 | 2021 | Wnt Family Member 9b (Wnt9b) Is a New Sensitive and Specific Marker for Breast Cancer. | 1 |
| 31867895 | 2020 | Circulating Exosomal miR-20b-5p Inhibition Restores Wnt9b Signaling and Reverses Diabetes-Associated Impaired Wound Healing. | 83 |
| 32887752 | 2020 | Canonical Wnts Mediate CD8(+) T Cell Noncytolytic Anti-HIV-1 Activity and Correlate with HIV-1 Clinical Status. | 11 |
| 31867895 | 2020 | Circulating Exosomal miR-20b-5p Inhibition Restores Wnt9b Signaling and Reverses Diabetes-Associated Impaired Wound Healing. | 83 |
| 32887752 | 2020 | Canonical Wnts Mediate CD8(+) T Cell Noncytolytic Anti-HIV-1 Activity and Correlate with HIV-1 Clinical Status. | 11 |
| 28915250 | 2017 | Multi-layered mutation in hedgehog-related genes in Gorlin syndrome may affect the phenotype. | 10 |
| 28915250 | 2017 | Multi-layered mutation in hedgehog-related genes in Gorlin syndrome may affect the phenotype. | 10 |
| 24437584 | 2015 | Association of WNT9B Gene Polymorphisms With Nonsyndromic Cleft Lip With or Without Cleft Palate in Brazilian Nuclear Families. | 15 |
| 26075712 | 2015 | Associations of Polymorphisms in WNT9B and PBX1 with Mayer-Rokitansky-Küster-Hauser Syndrome in Chinese Han. | 12 |
| 24437584 | 2015 | Association of WNT9B Gene Polymorphisms With Nonsyndromic Cleft Lip With or Without Cleft Palate in Brazilian Nuclear Families. | 15 |
Citation
Dessen P
WNT9B (Wnt family member 9B)
Atlas Genet Cytogenet Oncol Haematol. 2003-06-01
Online version: http://atlasgeneticsoncology.org/gene/42833/wnt9b
