Details for: TMEM165

Gene ID: 55858

Symbol: TMEM165

Ensembl ID: ENSG00000134851

Description: transmembrane protein 165

Associated with

Other Information

Genular Protein ID: 1044099067

Symbol: TM165_HUMAN

Name: Transmembrane protein 165

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 10931946

Title: Gene expression profiling in the human hypothalamus-pituitary-adrenal axis and full-length cDNA cloning.

PubMed ID: 10931946

DOI: 10.1073/pnas.160270997

PubMed ID: 14702039

Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.

PubMed ID: 14702039

DOI: 10.1038/ng1285

PubMed ID: 15815621

Title: Generation and annotation of the DNA sequences of human chromosomes 2 and 4.

PubMed ID: 15815621

DOI: 10.1038/nature03466

PubMed ID: 15489334

Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

PubMed ID: 15489334

DOI: 10.1101/gr.2596504

PubMed ID: 21269460

Title: Initial characterization of the human central proteome.

PubMed ID: 21269460

DOI: 10.1186/1752-0509-5-17

PubMed ID: 23575229

Title: Impact of disease-causing mutations on TMEM165 subcellular localization, a recently identified protein involved in CDG-II.

PubMed ID: 23575229

DOI: 10.1093/hmg/ddt146

PubMed ID: 27008884

Title: Glycosylation abnormalities in Gdt1p/TMEM165 deficient cells result from a defect in Golgi manganese homeostasis.

PubMed ID: 27008884

DOI: 10.1093/hmg/ddw026

PubMed ID: 32047108

Title: The human Golgi protein TMEM165 transports calcium and manganese in yeast and bacterial cells.

PubMed ID: 32047108

DOI: 10.1074/jbc.ra119.012249

PubMed ID: 23430531

Title: Bone dysplasia as a key feature in three patients with a novel congenital disorder of glycosylation (CDG) type II due to a deep intronic splice mutation in TMEM165.

PubMed ID: 23430531

DOI: 10.1007/8904_2012_172

PubMed ID: 23569283

Title: Newly characterized Golgi-localized family of proteins is involved in calcium and pH homeostasis in yeast and human cells.

PubMed ID: 23569283

DOI: 10.1073/pnas.1219871110

PubMed ID: 25944712

Title: N-terminome analysis of the human mitochondrial proteome.

PubMed ID: 25944712

DOI: 10.1002/pmic.201400617

PubMed ID: 22683087

Title: TMEM165 deficiency causes a congenital disorder of glycosylation.

PubMed ID: 22683087

DOI: 10.1016/j.ajhg.2012.05.002

Sequence Information:

  • Length: 324
  • Mass: 34906
  • Checksum: A0E6C8BBFF189D72
  • Sequence:
  • MAAAAPGNGR ASAPRLLLLF LVPLLWAPAA VRAGPDEDLS HRNKEPPAPA QQLQPQPVAV 
    QGPEPARVEK IFTPAAPVHT NKEDPATQTN LGFIHAFVAA ISVIIVSELG DKTFFIAAIM 
    AMRYNRLTVL AGAMLALGLM TCLSVLFGYA TTVIPRVYTY YVSTVLFAIF GIRMLREGLK 
    MSPDEGQEEL EEVQAELKKK DEEFQRTKLL NGPGDVETGT SITVPQKKWL HFISPIFVQA 
    LTLTFLAEWG DRSQLTTIVL AAREDPYGVA VGGTVGHCLC TGLAVIGGRM IAQKISVRTV 
    TIIGGIVFLA FAFSALFISP DSGF

Database document:

This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.