Details for: SPRY2
Associated with
Other Information
Genular Protein ID: 3050276979
Symbol: SPY2_HUMAN
Name: Protein sprouty homolog 2
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 9458049
Title: Sprouty encodes a novel antagonist of FGF signaling that patterns apical branching of the Drosophila airways.
PubMed ID: 9458049
PubMed ID: 14702039
Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.
PubMed ID: 14702039
DOI: 10.1038/ng1285
PubMed ID: 17974005
Title: The full-ORF clone resource of the German cDNA consortium.
PubMed ID: 17974005
PubMed ID: 15057823
Title: The DNA sequence and analysis of human chromosome 13.
PubMed ID: 15057823
DOI: 10.1038/nature02379
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: 10887178
Title: Sprouty proteins are targeted to membrane ruffles upon growth factor receptor tyrosine kinase activation. Identification of a novel translocation domain.
PubMed ID: 10887178
PubMed ID: 16877379
Title: A functional interaction between sprouty proteins and caveolin-1.
PubMed ID: 16877379
PubMed ID: 12717443
Title: Mammalian Sprouty4 suppresses Ras-independent ERK activation by binding to Raf1.
PubMed ID: 12717443
DOI: 10.1038/ncb978
PubMed ID: 17974561
Title: Tesk1 interacts with Spry2 to abrogate its inhibition of ERK phosphorylation downstream of receptor tyrosine kinase signaling.
PubMed ID: 17974561
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: 21288888
Title: Cleavage-site specificity of prolyl endopeptidase FAP investigated with a full-length protein substrate.
PubMed ID: 21288888
DOI: 10.1093/jb/mvr017
PubMed ID: 23186163
Title: Toward a comprehensive characterization of a human cancer cell phosphoproteome.
PubMed ID: 23186163
DOI: 10.1021/pr300630k
PubMed ID: 29408807
Title: Modifier variant of METTL13 suppresses human GAB1-associated profound deafness.
PubMed ID: 29408807
DOI: 10.1172/jci97350
PubMed ID: 25782674
Title: A SPRY2 mutation leading to MAPK/ERK pathway inhibition is associated with an autosomal dominant form of IgA nephropathy.
PubMed ID: 25782674
DOI: 10.1038/ejhg.2015.52
Sequence Information:
- Length: 315
- Mass: 34688
- Checksum: 8CC6256929D91A7E
- Sequence:
MEARAQSGNG SQPLLQTPRD GGRQRGEPDP RDALTQQVHV LSLDQIRAIR NTNEYTEGPT VVPRPGLKPA PRPSTQHKHE RLHGLPEHRQ PPRLQHSQVH SSARAPLSRS ISTVSSGSRS STRTSTSSSS SEQRLLGSSF SSGPVADGII RVQPKSELKP GELKPLSKED LGLHAYRCED CGKCKCKECT YPRPLPSDWI CDKQCLCSAQ NVIDYGTCVC CVKGLFYHCS NDDEDNCADN PCSCSQSHCC TRWSAMGVMS LFLPCLWCYL PAKGCLKLCQ GCYDRVNRPG CRCKNSNTVC CKVPTVPPRN FEKPT
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.