Details for: DPM3

Gene ID: 54344

Symbol: DPM3

Ensembl ID: ENSG00000179085

Description: dolichyl-phosphate mannosyltransferase subunit 3, regulatory

Associated with

Other Information

Genular Protein ID: 4126783512

Symbol: DPM3_HUMAN

Name: Dolichol-phosphate mannosyltransferase subunit 3

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 10835346

Title: Human dolichol-phosphate-mannose synthase consists of three subunits, DPM1, DPM2 and DPM3.

PubMed ID: 10835346

DOI: 10.1093/emboj/19.11.2475

PubMed ID: 11420690

Title: Dolichol-phosphate-mannose-3 (DPM3)/prostin-1 is a novel phospholipase C-gamma regulated gene negatively associated with prostate tumor invasion.

PubMed ID: 11420690

DOI: 10.1038/sj.onc.1204379

PubMed ID: 16710414

Title: The DNA sequence and biological annotation of human chromosome 1.

PubMed ID: 16710414

DOI: 10.1038/nature04727

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: 25944712

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

PubMed ID: 25944712

DOI: 10.1002/pmic.201400617

PubMed ID: 19576565

Title: Deficiency of Dol-P-Man synthase subunit DPM3 bridges the congenital disorders of glycosylation with the dystroglycanopathies.

PubMed ID: 19576565

DOI: 10.1016/j.ajhg.2009.06.006

PubMed ID: 28803818

Title: A homozygous DPM3 mutation in a patient with alpha-dystroglycan-related limb girdle muscular dystrophy.

PubMed ID: 28803818

DOI: 10.1016/j.nmd.2017.07.006

PubMed ID: 29246662

Title: Corrigendum to 'A homozygous DPM3 mutation in a patient with alpha-dystroglycan-related limb girdle muscular dystrophy' [Neuromuscular disorders 27/11 (2017) 1043-1046].

PubMed ID: 29246662

DOI: 10.1016/j.nmd.2017.11.012

PubMed ID: 31469168

Title: Novel mutations in DPM3 cause dystroglycanopathy with central nervous system involvement.

PubMed ID: 31469168

DOI: 10.1111/cge.13634

PubMed ID: 31266720

Title: Dilated cardiomyopathy and limb-girdle muscular dystrophy-dystroglycanopathy due to novel pathogenic variants in the DPM3 gene.

PubMed ID: 31266720

DOI: 10.1016/j.nmd.2019.05.004

Sequence Information:

  • Length: 92
  • Mass: 10094
  • Checksum: C350A6896842A877
  • Sequence:
  • MTKLAQWLWG LAILGSTWVA LTTGALGLEL PLSCQEVLWP LPAYLLVSAG CYALGTVGYR 
    VATFHDCEDA ARELQSQIQE ARADLARRGL RF

Genular Protein ID: 2422531140

Symbol: A0A140VJI4_HUMAN

Name: N/A

UniProtKB Accession Codes:

Database IDs:

Sequence Information:

  • Length: 122
  • Mass: 13277
  • Checksum: DD8661D41C2AE5C0
  • Sequence:
  • MLSVGGLRLS LVRFSFLLLR GALLPSLAVT MTKLAQWLWG LAILGSTWVA LTTGALGLEL 
    PLSCQEVLWP LPAYLLVSAG CYALGTVGYR VATFHDCEDA ARELQSQIQE ARADLARRGL 
    RF

Genular Protein ID: 1406424857

Symbol: Q86TM7_HUMAN

Name: N/A

UniProtKB Accession Codes:

Database IDs:

Citations:

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

Sequence Information:

  • Length: 94
  • Mass: 10294
  • Checksum: 83BEDEB19905CF61
  • Sequence:
  • VTMTKLAQWL WGLAILGSTW VALTTGALGL ELPLSCQEVL WPLPAYLLVS AGCYALGTVG 
    YRVATFHDCE DAARELQSQI QEARADLARR GLRF

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.