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Search results 301 to 360 out of 360 for Cd164

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0.057s
Type Details Score
Allele    
Name: CD164 antigen; wild type
Allele  
Name: CD164 sialomucin-like 2; wild type
Allele Type: Not Specified
Allele  
Name: CD164 antigen; gene trap OST33912, Lexicon Genetics
Allele Type: Gene trapped
Allele
Name: CD164 antigen; endonuclease-mediated mutation 1, Cyagen Biosciences
Allele Type: Endonuclease-mediated
Attribute String: Null/knockout
Publication
First Author: Zannettino AC
Year: 1998
Journal: Blood
Title: The sialomucin CD164 (MGC-24v) is an adhesive glycoprotein expressed by human hematopoietic progenitors and bone marrow stromal cells that serves as a potent negative regulator of hematopoiesis.
Volume: 92
Issue: 8
Pages: 2613-28
Allele
Name: CD164 antigen; targeted mutation 1a, Wellcome Trust Sanger Institute
Allele Type: Targeted
Attribute String: Conditional ready, Null/knockout, Reporter
Allele
Name: CD164 antigen; endonuclease-mediated mutation 1, Baylor College of Medicine
Allele Type: Endonuclease-mediated
Attribute String: Null/knockout
Allele
Name: CD164 antigen; endonuclease-mediated mutation 2, GemPharmatech Co., Ltd
Allele Type: Endonuclease-mediated
Attribute String: Null/knockout
Allele
Name: CD164 antigen; endonuclease-mediated mutation 1, GemPharmatech Co., Ltd
Allele Type: Endonuclease-mediated
Attribute String: Conditional ready, No functional change
Allele  
Name: CD164 antigen; gene trap D157G01, German Gene Trap Consortium
Allele Type: Gene trapped
Strain
Attribute String: coisogenic, endonuclease-mediated mutation, mutant strain
Allele
Name: CD164 sialomucin-like 2; endonuclease-mediated mutation 2, GemPharmatech Co., Ltd
Allele Type: Endonuclease-mediated
Attribute String: Null/knockout
Allele
Name: CD164 sialomucin-like 2; endonuclease-mediated mutation 1, GemPharmatech Co., Ltd
Allele Type: Endonuclease-mediated
Attribute String: Conditional ready, No functional change
Allele  
Name: CD164 sialomucin-like 2; gene trap OST14023, Lexicon Genetics
Allele Type: Gene trapped
Allele
Name: CD164 sialomucin-like 2; targeted mutation 1, Lexicon Pharmaceuticals
Allele Type: Targeted
Attribute String: Null/knockout
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus caroli
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus pahari
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus spretus
GXD Expression
Probe: MGI:6455044
Assay Type: RNA in situ
Annotation Date: 2020-09-14
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1760027
Pattern: Regionally restricted
Stage: TS27
Assay Id: MGI:6455074
Age: postnatal day 1
Image: 2c
Note: Expression is restricted to the hair cells (inner and outer).
Specimen Label: 2c
Detected: true
Specimen Num: 1
DO Term
Strain
Attribute String: coisogenic, endonuclease-mediated mutation, mutant strain
Allele
Name: CD164 sialomucin-like 2; targeted mutation 1, Mouse Biology Program, UC Davis
Allele Type: Targeted
Attribute String: Null/knockout, Reporter
Strain
Attribute String: mutant stock, targeted mutation
Strain
Attribute String: mutant stock, targeted mutation
Publication
First Author: Nyegaard M
Year: 2015
Journal: PLoS Genet
Title: A Novel Locus Harbouring a Functional CD164 Nonsense Mutation Identified in a Large Danish Family with Nonsyndromic Hearing Impairment.
Volume: 11
Issue: 7
Pages: e1005386
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Publication
First Author: Endo Y
Year: 2004
Journal: Genomics
Title: Identification of the mouse H-ficolin gene as a pseudogene and orthology between mouse ficolins A/B and human L-/M-ficolins.
Volume: 84
Issue: 4
Pages: 737-44
Publication
First Author: Chan JY
Year: 2001
Journal: J Biol Chem
Title: Relationship between novel isoforms, functionally important domains, and subcellular distribution of CD164/endolyn.
Volume: 276
Issue: 3
Pages: 2139-52
Protein
Organism: Mus musculus/domesticus
Length: 197  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 195  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 162  
Fragment?: true
Protein
Organism: Mus musculus/domesticus
Length: 24  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 197  
Fragment?: true
Protein
Organism: Mus musculus/domesticus
Length: 161  
Fragment?: true
Protein Domain
Type: Family
Description: CD164 is a mucin-like receptor, or sialomucin, with specificity inreceptor/ligand interactions that depends on the structural characteristics of themucin-like receptor. Its functions include mediating, or regulating,haematopoietic progenitor cell adhesion and the negative regulation of theirgrowth and/or-differentiation. It exists in the native state as adisulphide-linked homodimer of two 80-85kDa subunits. It is usually expressed by CD34+and CD341o/- haematopoietic stem cells and associated microenvironmentalcells. It contains, in its extracellular region, two mucin domains (I andII)linked by a non-mucin domain, which has been predicted to contain intra-disulphide bridges. This receptor may play a key role in haematopoiesisby facilitating the adhesion of human CD34+ cells to bone marrow stroma andby negatively regulating CD34+ CD341o/- haematopoietic progenitor cellproliferation. These effects involve the CD164 class I and/or II epitopesrecognised by the monoclonal antibodies (mAbs) 105A5 and 103B2/9E10. Theseepitopes are carbohydrate-dependent and are located on the N-terminalmucin domain I [, ].It has been found that murine MGC-24v and rat endolyn share significantsequence similarities with human CD164. However, CD164 lacks the consensusglycosaminoglycan (GAG)-attachment site found in MGC-24; it is possiblethat GAG-association is responsible for the high molecular weight of theepithelial-derived MGC-24 glycoprotein [].Genomic structure studies have placed CD164 within the mucin-subgroupthatcomprises multiple exons, and demonstrate the diverse chromosomaldistribution of this family of molecules. Molecules with such multipleexons may have sophisticated regulatory mechanisms that involve not onlypost-translational modifications of the oligosaccharide side chains, butalso differential exon usage. Although differences in the intron and exonsizes are seen between the mouse and human genes, the predicted proteinsare similar in size and structure, maintaining functionally importantmotifs that regulate cell proliferation or subcellular distribution [].CD164 is a gene whose expression depends on differential usage of poly-adenylation sites within the 3'-UTR. The conserved distribution of the3.2- and 1.2-kb CD164 transcripts between mouse and human suggests that(i) a mechanism may exist to regulate tissue-specific polyadenylation, and(ii) differences in polyadenylation are important for the expression andfunction of CD164 in different tissues. Two other aspects of the structureof CD164 are of particular interest. First, it shares one of severalconserved features of a cytokine-binding pocket - in this respect, it isnotable that evidence exists for a class of cell-surface sialomucinmodulators that directly interact with growth factor receptors to regulatetheir response to physiological ligands. Second, its cytoplasmic tailcontains a C-terminal YHTL motif found in many endocytic membrane proteinsor receptors. These Tyr-based motifs bind to adaptor proteins, which mediatethe sorting of membrane proteins into transport vesicles from the plasmamembrane to the endosomes, and between intracellular compartments.
Publication
First Author: Kolla L
Year: 2020
Journal: Nat Commun
Title: Characterization of the development of the mouse cochlear epithelium at the single cell level.
Volume: 11
Issue: 1
Pages: 2389
Publication
First Author: Tang T
Year: 2010
Journal: Nat Biotechnol
Title: A mouse knockout library for secreted and transmembrane proteins.
Volume: 28
Issue: 7
Pages: 749-55
Publication      
First Author: Lexicon Genetics, Inc
Year: 2011
Journal: Database Download
Title: MGI download of Lexicon knockout data
Publication      
First Author: University of California, Davis
Year: 2010
Journal: MGI Direct Data Submission
Title: Alleles produced for the KOMP project by the University of California, Davis
Publication      
First Author: Mouse Genome Informatics Scientific Curators
Year: 2003
Journal: Database Download
Title: Integrating Computational Gene Models into the Mouse Genome Informatics (MGI) Database
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2002
Title: Function or Process or Component Unknown following Literature Review
Publication
First Author: Gerhard DS
Year: 2004
Journal: Genome Res
Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
Volume: 14
Issue: 10B
Pages: 2121-7
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2002
Title: Chromosome assignment of mouse genes using the Mouse Genome Sequencing Consortium (MGSC) assembly and the ENSEMBL Database
Publication
First Author: Church DM
Year: 2009
Journal: PLoS Biol
Title: Lineage-specific biology revealed by a finished genome assembly of the mouse.
Volume: 7
Issue: 5
Pages: e1000112