Details for: REEP1
Associated with
Other Information
Genular Protein ID: 2452348930
Symbol: REEP1_HUMAN
Name: Receptor expression-enhancing protein 1
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 15550249
Title: RTP family members induce functional expression of mammalian odorant receptors.
PubMed ID: 15550249
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: 16720576
Title: Members of RTP and REEP gene families influence functional bitter taste receptor expression.
PubMed ID: 16720576
PubMed ID: 19690332
Title: Quantitative phosphoproteomic analysis of T cell receptor signaling reveals system-wide modulation of protein-protein interactions.
PubMed ID: 19690332
PubMed ID: 20200447
Title: Hereditary spastic paraplegia proteins REEP1, spastin, and atlastin-1 coordinate microtubule interactions with the tubular ER network.
PubMed ID: 20200447
DOI: 10.1172/jci40979
PubMed ID: 22703882
Title: Exome sequencing identifies a REEP1 mutation involved in distal hereditary motor neuropathy type V.
PubMed ID: 22703882
PubMed ID: 23186163
Title: Toward a comprehensive characterization of a human cancer cell phosphoproteome.
PubMed ID: 23186163
DOI: 10.1021/pr300630k
PubMed ID: 23969831
Title: Protrudin binds atlastins and endoplasmic reticulum-shaping proteins and regulates network formation.
PubMed ID: 23969831
PubMed ID: 24478229
Title: Functional mutation analysis provides evidence for a role of REEP1 in lipid droplet biology.
PubMed ID: 24478229
DOI: 10.1002/humu.22521
PubMed ID: 24275569
Title: An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome.
PubMed ID: 24275569
PubMed ID: 18644145
Title: Autosomal dominant hereditary spastic paraplegia: novel mutations in the REEP1 gene (SPG31).
PubMed ID: 18644145
PubMed ID: 16826527
Title: Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31.
PubMed ID: 16826527
DOI: 10.1086/505361
PubMed ID: 20718791
Title: Mutation screening of spastin, atlastin, and REEP1 in hereditary spastic paraplegia.
PubMed ID: 20718791
PubMed ID: 21618648
Title: REEP1 mutations in SPG31: frequency, mutational spectrum, and potential association with mitochondrial morpho-functional dysfunction.
PubMed ID: 21618648
DOI: 10.1002/humu.21542
PubMed ID: 27066569
Title: Recessive REEP1 mutation is associated with congenital axonal neuropathy and diaphragmatic palsy.
PubMed ID: 27066569
PubMed ID: 31872057
Title: Further supporting evidence for REEP1 phenotypic and allelic heterogeneity.
PubMed ID: 31872057
PubMed ID: 34193129
Title: Novel homozygous mutations in Pakistani families with Charcot-Marie-Tooth disease.
PubMed ID: 34193129
Sequence Information:
- Length: 201
- Mass: 22255
- Checksum: 98F120DE100276A9
- Sequence:
MVSWIISRLV VLIFGTLYPA YYSYKAVKSK DIKEYVKWMM YWIIFALFTT AETFTDIFLC WFPFYYELKI AFVAWLLSPY TKGSSLLYRK FVHPTLSSKE KEIDDCLVQA KDRSYDALVH FGKRGLNVAA TAAVMAASKG QGALSERLRS FSMQDLTTIR GDGAPAPSGP PPPGSGRASG KHGQPKMSRS ASESASSSGT A
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.