Fzd9 | ENSMUSG00000049551 | NCBI 14371

Details for: Fzd9

Gene ID: 14371

Symbol: Fzd9

Ensembl ID: ENSMUSG00000049551

Description: frizzled class receptor 9

Associated with

B cell differentiation
(GO:0030183)
Bone regeneration
(GO:1990523)
Canonical wnt signaling pathway
(GO:0060070)
Cell surface
(GO:0009986)
Cell surface receptor signaling pathway
(GO:0007166)
Cytoplasm
(GO:0005737)
Filopodium membrane
(GO:0031527)
Glutamatergic synapse
(GO:0098978)
G protein-coupled receptor activity
(GO:0004930)
G protein-coupled receptor signaling pathway
(GO:0007186)
Learning or memory
(GO:0007611)
Membrane
(GO:0016020)
Multicellular organism development
(GO:0007275)
Negative regulation of neuron apoptotic process
(GO:0043524)
Negative regulation of skeletal muscle acetylcholine-gated channel clustering
(GO:1904394)
Neuroblast proliferation
(GO:0007405)
Non-canonical wnt signaling pathway
(GO:0035567)
Ossification
(GO:0001503)
Perinuclear region of cytoplasm
(GO:0048471)
Plasma membrane
(GO:0005886)
Positive regulation of bone mineralization
(GO:0030501)
Positive regulation of canonical wnt signaling pathway
(GO:0090263)
Positive regulation of neural precursor cell proliferation
(GO:2000179)
Postsynapse
(GO:0098794)
Postsynapse organization
(GO:0099173)
Protein heterodimerization activity
(GO:0046982)
Protein homodimerization activity
(GO:0042803)
Regulation of cell cycle
(GO:0051726)
Regulation of postsynaptic cytosolic calcium ion concentration
(GO:0099566)
Regulation of skeletal muscle acetylcholine-gated channel clustering
(GO:1904393)
Signal transduction
(GO:0007165)
Transmembrane signaling receptor activity
(GO:0004888)
Wnt-protein binding
(GO:0017147)
Wnt receptor activity
(GO:0042813)
Wnt signaling pathway
(GO:0016055)

Other Information

Proteins

Frizzled-9

Genular Protein ID: 19881233

Symbol: FZD9_MOUSE

Name: Frizzled-9

UniProtKB Accession Codes:

Q9R216 O35494 Q9CX16 Q9R2B3

Database IDs:

Citations:

PubMed ID: 10198163

Title: Characterization and expression pattern of the frizzled gene Fzd9, the mouse homolog of FZD9 which is deleted in Williams-Beuren syndrome.

PubMed ID: 10198163

DOI: 10.1006/geno.1999.5773

PubMed ID: 16141072

Title: The transcriptional landscape of the mammalian genome.

PubMed ID: 16141072

DOI: 10.1126/science.1112014

PubMed ID: 15930120

Title: Hippocampal and visuospatial learning defects in mice with a deletion of frizzled 9, a gene in the Williams syndrome deletion interval.

PubMed ID: 15930120

DOI: 10.1242/dev.01871

PubMed ID: 21402791

Title: Control of bone formation by the serpentine receptor Frizzled-9.

PubMed ID: 21402791

DOI: 10.1083/jcb.201008012

PubMed ID: 24391920

Title: The Wnt serpentine receptor Frizzled-9 regulates new bone formation in fracture healing.

PubMed ID: 24391920

DOI: 10.1371/journal.pone.0084232

PubMed ID: 24860427

Title: Frizzled-9 impairs acetylcholine receptor clustering in skeletal muscle cells.

PubMed ID: 24860427

DOI: 10.3389/fncel.2014.00110

Sequence Information:

Length: 592
Mass: 64995
Checksum: 21B2D4F8CE232965
Sequence:

MAVPPLLRGA LLLWQLLATG GAALEIGRFD PERGRGPAPC QAMEIPMCRG IGYNLTRMPN 
LLGHTSQGEA AAQLAEFSPL VQYGCHSHLR FFLCSLYAPM CTDQVSTPIP ACRPMCEQAR 
LRCAPIMEQF NFGWPDSLDC ARLPTRNDPH ALCMEAPENA TAGPTEPHKG LGMLPVAPRP 
ARPPGDSAPG PGSGGTCDNP EKFQYVEKSR SCAPRCGPGV EVFWSRRDKD FALVWMAVWS 
ALCFFSTAFT VFTFLLEPHR FQYPERPIIF LSMCYNVYSL AFLIRAVAGA QSVACDQEAG 
ALYVIQEGLE NTGCTLVFLL LYYFGMASSL WWVVLTLTWF LAAGKKWGHE AIEAHGSYFH 
MAAWGLPALK TIVVLTLRKV AGDELTGLCY VASMDPAALT GFVLVPLSCY LVLGTSFLLT 
GFVALFHIRK IMKTGGTNTE KLEKLMVKIG VFSILYTVPA TCVIVCYVYE RLNMDFWRLR 
ATEQPCTAAT VPGGRRDCSL PGGSVPTVAV FMLKIFMSLV VGITSGVWVW SSKTFQTWQS 
LCYRKMAAGR ARAKACRTPG GYGRGTHCHY KAPTVVLHMT KTDPSLENPT HL

The gene details are incomplete or unavailable at the moment.

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.

Details for: Fzd9

Associated with

Other Information

Characterization and expression pattern of the frizzled gene Fzd9, the mouse homolog of FZD9 which is deleted in Williams-Beuren syndrome. PubMed ID: 10198163

The transcriptional landscape of the mammalian genome. PubMed ID: 16141072

Hippocampal and visuospatial learning defects in mice with a deletion of frizzled 9, a gene in the Williams syndrome deletion interval. PubMed ID: 15930120

Control of bone formation by the serpentine receptor Frizzled-9. PubMed ID: 21402791

The Wnt serpentine receptor Frizzled-9 regulates new bone formation in fracture healing. PubMed ID: 24391920