Identity
HGNC
LOCATION
4q34.3
LOCUSID
ALIAS
MCOPCB9,MCOPS15,ODZ3,TEN3,TNM3,Ten-m3,ten-3
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: 55714
MIM: 610083
HGNC: 29944
Ensembl: ENSG00000218336
Variants:
dbSNP: 55714
ClinVar: 55714
TCGA: ENSG00000218336
COSMIC: TENM3
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000218336 | ENST00000510504 | H0YAF0 |
| ENSG00000218336 | ENST00000511685 | Q9P273 |
| ENSG00000218336 | ENST00000511685 | A0A140VJW8 |
| ENSG00000218336 | ENST00000512480 | D6RGC5 |
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 32960451 | 2021 | Ten-m/Odz3 regulates migration and differentiation of chondrogenic ATDC5 cells via RhoA-mediated actin reorganization. | 2 |
| 34174923 | 2021 | Replicative verification of susceptibility genes previously identified from families with segregating developmental dysplasia of the hip. | 1 |
| 32960451 | 2021 | Ten-m/Odz3 regulates migration and differentiation of chondrogenic ATDC5 cells via RhoA-mediated actin reorganization. | 2 |
| 34174923 | 2021 | Replicative verification of susceptibility genes previously identified from families with segregating developmental dysplasia of the hip. | 1 |
| 32799327 | 2020 | Exome sequencing in patients with microphthalmia, anophthalmia, and coloboma (MAC) from a consanguineous population. | 5 |
| 32799327 | 2020 | Exome sequencing in patients with microphthalmia, anophthalmia, and coloboma (MAC) from a consanguineous population. | 5 |
| 29753094 | 2019 | Sequence variations in TENM3 gene causing eye anomalies with intellectual disability: Expanding the phenotypic spectrum. | 8 |
| 30273960 | 2019 | Novel mutation in Teneurin 3 found to co-segregate in all affecteds in a multi-generation family with developmental dysplasia of the hip. | 13 |
| 29753094 | 2019 | Sequence variations in TENM3 gene causing eye anomalies with intellectual disability: Expanding the phenotypic spectrum. | 8 |
| 30273960 | 2019 | Novel mutation in Teneurin 3 found to co-segregate in all affecteds in a multi-generation family with developmental dysplasia of the hip. | 13 |
| 27103084 | 2016 | Confirmation of TENM3 involvement in autosomal recessive colobomatous microphthalmia. | 17 |
| 27103084 | 2016 | Confirmation of TENM3 involvement in autosomal recessive colobomatous microphthalmia. | 17 |
| 22766609 | 2012 | Homozygous null mutation in ODZ3 causes microphthalmia in humans. | 32 |
| 22766609 | 2012 | Homozygous null mutation in ODZ3 causes microphthalmia in humans. | 32 |
| 20379614 | 2010 | Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. | 78 |
Citation
Dessen P
TENM3 (teneurin transmembrane protein 3)
Atlas Genet Cytogenet Oncol Haematol. 2003-05-01
Online version: http://atlasgeneticsoncology.org/gene/41604/tenm3
