Details for: Wnt1
Associated with
Other Information
Genular Protein ID: 1136332274
Symbol: WNT1_MOUSE
Name: Proto-oncogene Wnt-1
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 6091914
Title: Structure and nucleotide sequence of the putative mammary oncogene int-1; proviral insertions leave the protein-encoding domain intact.
PubMed ID: 6091914
PubMed ID: 3018519
Title: Nucleotide sequence and expression in vitro of cDNA derived from mRNA of int-1, a provirally activated mouse mammary oncogene.
PubMed ID: 3018519
PubMed ID: 2279700
Title: Expression of multiple novel Wnt-1/int-1-related genes during fetal and adult mouse development.
PubMed ID: 2279700
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: 2202907
Title: Targeted disruption of the murine int-1 proto-oncogene resulting in severe abnormalities in midbrain and cerebellar development.
PubMed ID: 2202907
DOI: 10.1038/346847a0
PubMed ID: 3594565
Title: Expression of the proto-oncogene int-1 is restricted to specific neural cells in the developing mouse embryo.
PubMed ID: 3594565
PubMed ID: 3594566
Title: Expression of the proto-oncogene int-1 is restricted to postmeiotic male germ cells and the neural tube of mid-gestational embryos.
PubMed ID: 3594566
PubMed ID: 10866835
Title: The evolutionarily conserved porcupine gene family is involved in the processing of the Wnt family.
PubMed ID: 10866835
PubMed ID: 15454084
Title: Mammalian Ryk is a Wnt coreceptor required for stimulation of neurite outgrowth.
PubMed ID: 15454084
PubMed ID: 16116452
Title: Ryk-mediated Wnt repulsion regulates posterior-directed growth of corticospinal tract.
PubMed ID: 16116452
DOI: 10.1038/nn1520
PubMed ID: 16543246
Title: Mouse cristin/R-spondin family proteins are novel ligands for the Frizzled 8 and LRP6 receptors and activate beta-catenin-dependent gene expression.
PubMed ID: 16543246
PubMed ID: 19841259
Title: Reciprocal regulation of Wnt and Gpr177/mouse Wntless is required for embryonic axis formation.
PubMed ID: 19841259
PubMed ID: 23499309
Title: Mutations in WNT1 cause different forms of bone fragility.
PubMed ID: 23499309
PubMed ID: 23656646
Title: WNT1 mutations in early-onset osteoporosis and osteogenesis imperfecta.
PubMed ID: 23656646
Sequence Information:
- Length: 370
- Mass: 41086
- Checksum: 02EEB23109231A40
- Sequence:
MGLWALLPSW VSTTLLLALT ALPAALAANS SGRWWGIVNI ASSTNLLTDS KSLQLVLEPS LQLLSRKQRR LIRQNPGILH SVSGGLQSAV RECKWQFRNR RWNCPTAPGP HLFGKIVNRG CRETAFIFAI TSAGVTHSVA RSCSEGSIES CTCDYRRRGP GGPDWHWGGC SDNIDFGRLF GREFVDSGEK GRDLRFLMNL HNNEAGRTTV FSEMRQECKC HGMSGSCTVR TCWMRLPTLR AVGDVLRDRF DGASRVLYGN RGSNRASRAE LLRLEPEDPA HKPPSPHDLV YFEKSPNFCT YSGRLGTAGT AGRACNSSSP ALDGCELLCC GRGHRTRTQR VTERCNCTFH WCCHVSCRNC THTRVLHECL
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.