Details for: TMEM106B
Associated with
Other Information
Genular Protein ID: 1555004101
Symbol: T106B_HUMAN
Name: N/A
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 14702039
Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.
PubMed ID: 14702039
DOI: 10.1038/ng1285
PubMed ID: 12690205
Title: Human chromosome 7: DNA sequence and biology.
PubMed ID: 12690205
PubMed ID: 12853948
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: 17081983
Title: Global, in vivo, and site-specific phosphorylation dynamics in signaling networks.
PubMed ID: 17081983
PubMed ID: 19159218
Title: Glycoproteomics analysis of human liver tissue by combination of multiple enzyme digestion and hydrazide chemistry.
PubMed ID: 19159218
DOI: 10.1021/pr8008012
PubMed ID: 20154673
Title: Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions.
PubMed ID: 20154673
DOI: 10.1038/ng.536
PubMed ID: 20068231
Title: Quantitative phosphoproteomics reveals widespread full phosphorylation site occupancy during mitosis.
PubMed ID: 20068231
PubMed ID: 21178100
Title: TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers.
PubMed ID: 21178100
PubMed ID: 22511793
Title: Membrane orientation and subcellular localization of transmembrane protein 106B (TMEM106B), a major risk factor for frontotemporal lobar degeneration.
PubMed ID: 22511793
PubMed ID: 22895706
Title: TMEM106B, the risk gene for frontotemporal dementia, is regulated by the microRNA-132/212 cluster and affects progranulin pathways.
PubMed ID: 22895706
PubMed ID: 23136129
Title: The frontotemporal lobar degeneration risk factor, TMEM106B, regulates lysosomal morphology and function.
PubMed ID: 23136129
DOI: 10.1093/hmg/dds475
PubMed ID: 23742080
Title: TMEM106B p.T185S regulates TMEM106B protein levels: implications for frontotemporal dementia.
PubMed ID: 23742080
DOI: 10.1111/jnc.12329
PubMed ID: 23186163
Title: Toward a comprehensive characterization of a human cancer cell phosphoproteome.
PubMed ID: 23186163
DOI: 10.1021/pr300630k
PubMed ID: 24488309
PubMed ID: 24442578
Title: TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions.
PubMed ID: 24442578
PubMed ID: 24385136
Title: TMEM106B protects C9ORF72 expansion carriers against frontotemporal dementia.
PubMed ID: 24385136
PubMed ID: 24357581
Title: The FTLD risk factor TMEM106B and MAP6 control dendritic trafficking of lysosomes.
PubMed ID: 24357581
PubMed ID: 25066864
Title: Lysosome size, motility and stress response regulated by fronto-temporal dementia modifier TMEM106B.
PubMed ID: 25066864
PubMed ID: 25255805
Title: Global profiling of co- and post-translationally N-myristoylated proteomes in human cells.
PubMed ID: 25255805
DOI: 10.1038/ncomms5919
PubMed ID: 28728022
Title: Loss of TMEM106B ameliorates lysosomal and frontotemporal dementia-related phenotypes in progranulin-deficient mice.
PubMed ID: 28728022
PubMed ID: 33333024
Title: Genetic Screens Identify Host Factors for SARS-CoV-2 and Common Cold Coronaviruses.
PubMed ID: 33333024
PubMed ID: 33686287
Title: Genome-wide CRISPR screening identifies TMEM106B as a proviral host factor for SARS-CoV-2.
PubMed ID: 33686287
PubMed ID: 35247328
Title: Homotypic fibrillization of TMEM106B across diverse neurodegenerative diseases.
PubMed ID: 35247328
PubMed ID: 35344984
Title: Amyloid fibrils in FTLD-TDP are composed of TMEM106B and not TDP-43.
PubMed ID: 35344984
PubMed ID: 35344985
Title: Age-dependent formation of TMEM106B amyloid filaments in human brains.
PubMed ID: 35344985
PubMed ID: 37421949
Title: TMEM106B is a receptor mediating ACE2-independent SARS-CoV-2 cell entry.
PubMed ID: 37421949
PubMed ID: 29186371
Title: A recurrent de novo mutation in TMEM106B causes hypomyelinating leukodystrophy.
PubMed ID: 29186371
DOI: 10.1093/brain/awx314
PubMed ID: 29444210
Title: The recurrent mutation in TMEM106B also causes hypomyelinating leukodystrophy in China and is a CpG hotspot.
PubMed ID: 29444210
DOI: 10.1093/brain/awy029
Sequence Information:
- Length: 274
- Mass: 31127
- Checksum: 906C923986DC04E6
- Sequence:
MGKSLSHLPL HSSKEDAYDG VTSENMRNGL VNSEVHNEDG RNGDVSQFPY VEFTGRDSVT CPTCQGTGRI PRGQENQLVA LIPYSDQRLR PRRTKLYVMA SVFVCLLLSG LAVFFLFPRS IDVKYIGVKS AYVSYDVQKR TIYLNITNTL NITNNNYYSV EVENITAQVQ FSKTVIGKAR LNNITIIGPL DMKQIDYTVP TVIAEEMSYM YDFCTLISIK VHNIVLMMQV TVTTTYFGHS EQISQERYQY VDCGRNTTYQ LGQSEYLNVL QPQQ
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.