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: 84910
MIM: 617203
HGNC: 25913
Ensembl: ENSG00000153214
Variants:
dbSNP: 84910
ClinVar: 84910
TCGA: ENSG00000153214
COSMIC: TMEM87B
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 24694933 | 2014 | Functional analysis of candidate genes in 2q13 deletion syndrome implicates FBLN7 and TMEM87B deficiency in congenital heart defects and FBLN7 in craniofacial malformations. | 25 |
| 24694933 | 2014 | Functional analysis of candidate genes in 2q13 deletion syndrome implicates FBLN7 and TMEM87B deficiency in congenital heart defects and FBLN7 in craniofacial malformations. | 25 |
Citation
Dessen P
TMEM87B (transmembrane protein 87B)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/74986/tmem87b-(transmembrane-protein-87b)
