TMEM87B (transmembrane protein 87B)

2014-11-01  

Identity

HGNC
LOCATION
2q13
LOCUSID
ALIAS
-
FUSION GENES

Other Information

Locus ID:

NCBI: 84910
MIM: 617203
HGNC: 25913
Ensembl: ENSG00000153214

Variants:

dbSNP: 84910
ClinVar: 84910
TCGA: ENSG00000153214
COSMIC: TMEM87B

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000153214ENST00000283206Q96K49
ENSG00000153214ENST00000452029H7C1G1
ENSG00000153214ENST00000452614H7C0B3
ENSG00000153214ENST00000649734A0A3B3IU29
ENSG00000153214ENST00000650799A0A494BZZ8

Expression (GTEx)

0
5
10
15
20
25
30

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
246949332014Functional analysis of candidate genes in 2q13 deletion syndrome implicates FBLN7 and TMEM87B deficiency in congenital heart defects and FBLN7 in craniofacial malformations.11

Citation

Dessen P

TMEM87B (transmembrane protein 87B)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/74986/tmem87b