TMEM185A (transmembrane protein 185A)

2014-11-01  

Identity

HGNC
LOCATION
Xq28
LOCUSID
ALIAS
CXorf13,FAM11A,FRAXF,ee3
FUSION GENES

Other Information

Locus ID:

NCBI: 84548
MIM: 300031
HGNC: 17125
Ensembl: ENSG00000269556

Variants:

dbSNP: 84548
ClinVar: 84548
TCGA: ENSG00000269556
COSMIC: TMEM185A

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000269556ENST00000502618H0YBJ6
ENSG00000269556ENST00000502858H0YAP3
ENSG00000269556ENST00000502900E5RFI9
ENSG00000269556ENST00000507237E7EMM1
ENSG00000269556ENST00000511776E5RGV1
ENSG00000269556ENST00000600449Q8NFB2
ENSG00000269556ENST00000611119B7Z4G6
ENSG00000269556ENST00000612022A0A087X081
ENSG00000269556ENST00000613273B3KY49

Expression (GTEx)

0
5
10
15
20
25

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
155253542004Cloning of a novel neuronally expressed orphan G-protein-coupled receptor which is up-regulated by erythropoietin, interacts with microtubule-associated protein 1b and colocalizes with the 5-hydroxytryptamine 2a receptor.6
155253542004Cloning of a novel neuronally expressed orphan G-protein-coupled receptor which is up-regulated by erythropoietin, interacts with microtubule-associated protein 1b and colocalizes with the 5-hydroxytryptamine 2a receptor.6
128064922003Genetic and neurological evaluation in a sample of individuals with pervasive developmental disorders.1
128064922003Genetic and neurological evaluation in a sample of individuals with pervasive developmental disorders.1
124041112002A novel gene, FAM11A, associated with the FRAXF CpG island is transcriptionally silent in FRAXF full mutation.6
124041112002A novel gene, FAM11A, associated with the FRAXF CpG island is transcriptionally silent in FRAXF full mutation.6

Citation

Dessen P

TMEM185A (transmembrane protein 185A)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/74850/tmem185a-(transmembrane-protein-185a)