WNT9B (Wnt family member 9B)

2003-06-01  

Identity

HGNC
LOCATION
17q21.32
LOCUSID
ALIAS
WNT14B,WNT15
FUSION GENES

Other Information

Locus ID:

NCBI: 7484
MIM: 602864
HGNC: 12779
Ensembl: ENSG00000158955

Variants:

dbSNP: 7484
ClinVar: 7484
TCGA: ENSG00000158955
COSMIC: WNT9B

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000158955ENST00000290015O14905
ENSG00000158955ENST00000393461E7EPC3
ENSG00000158955ENST00000575372I3L0L8

Expression (GTEx)

0
1
2
3

Pathways

PathwaySourceExternal ID
mTOR signaling pathwayKEGGko04150
Wnt signaling pathwayKEGGko04310
MelanogenesisKEGGko04916
Basal cell carcinomaKEGGko05217
mTOR signaling pathwayKEGGhsa04150
Wnt signaling pathwayKEGGhsa04310
MelanogenesisKEGGhsa04916
Pathways in cancerKEGGhsa05200
Basal cell carcinomaKEGGhsa05217
HTLV-I infectionKEGGko05166
HTLV-I infectionKEGGhsa05166
Hippo signaling pathwayKEGGhsa04390
Hippo signaling pathwayKEGGko04390
Proteoglycans in cancerKEGGhsa05205
Proteoglycans in cancerKEGGko05205
Signaling pathways regulating pluripotency of stem cellsKEGGhsa04550
Signaling pathways regulating pluripotency of stem cellsKEGGko04550
Wnt signalingKEGGhsa_M00677
Wnt signalingKEGGM00677
Signal TransductionREACTOMER-HSA-162582
Signaling by GPCRREACTOMER-HSA-372790
GPCR ligand bindingREACTOMER-HSA-500792
Class B/2 (Secretin family receptors)REACTOMER-HSA-373080
Signaling by WntREACTOMER-HSA-195721
WNT ligand biogenesis and traffickingREACTOMER-HSA-3238698
Breast cancerKEGGko05224
Breast cancerKEGGhsa05224

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
337048242021Genetic Variation in WNT9B Increases Relapse Hazard in Multiple Sclerosis.6
341457442021Homozygous WNT9B variants in two families with bilateral renal agenesis/hypoplasia/dysplasia.2
343244582021Wnt Family Member 9b (Wnt9b) Is a New Sensitive and Specific Marker for Breast Cancer.1
337048242021Genetic Variation in WNT9B Increases Relapse Hazard in Multiple Sclerosis.6
341457442021Homozygous WNT9B variants in two families with bilateral renal agenesis/hypoplasia/dysplasia.2
343244582021Wnt Family Member 9b (Wnt9b) Is a New Sensitive and Specific Marker for Breast Cancer.1
318678952020Circulating Exosomal miR-20b-5p Inhibition Restores Wnt9b Signaling and Reverses Diabetes-Associated Impaired Wound Healing.83
328877522020Canonical Wnts Mediate CD8(+) T Cell Noncytolytic Anti-HIV-1 Activity and Correlate with HIV-1 Clinical Status.11
318678952020Circulating Exosomal miR-20b-5p Inhibition Restores Wnt9b Signaling and Reverses Diabetes-Associated Impaired Wound Healing.83
328877522020Canonical Wnts Mediate CD8(+) T Cell Noncytolytic Anti-HIV-1 Activity and Correlate with HIV-1 Clinical Status.11
289152502017Multi-layered mutation in hedgehog-related genes in Gorlin syndrome may affect the phenotype.10
289152502017Multi-layered mutation in hedgehog-related genes in Gorlin syndrome may affect the phenotype.10
244375842015Association of WNT9B Gene Polymorphisms With Nonsyndromic Cleft Lip With or Without Cleft Palate in Brazilian Nuclear Families.15
260757122015Associations of Polymorphisms in WNT9B and PBX1 with Mayer-Rokitansky-Küster-Hauser Syndrome in Chinese Han.12
244375842015Association 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/gene-fusions/welcome