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Search results 101 to 116 out of 116 for Dpy19l1

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Type Details Score
Publication
- | J:53168
     
First Author: Bairoch A
Year: 1999
Journal: Database Release
Title: SWISS-PROT Annotated protein sequence database
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Publication
- | J:91388
       
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and Loading Genome Assembly Coordinates from Ensembl Annotations
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Publication
- | J:155221
     
First Author: Mouse Genome Informatics
Year: 2010
Journal: Database Release
Title: Protein Ontology Association Load.
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Publication
- | J:90438
       
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and loading genome assembly coordinates from NCBI annotations
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Publication
- | J:144087
     
First Author: Mouse Genome Informatics Scientific Curators
Year: 2009
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Genome 430 2.0 Array Platform
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UniProt Feature
UniProt Feature
Begin: 1
Description: Probable C-mannosyltransferase DPY19L1
Type: chain
End: 746
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Protein
A6X919-3
Organism: Mus musculus/domesticus
Length: 195  
Fragment?: false
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Protein
A6X919-2
Organism: Mus musculus/domesticus
Length: 552  
Fragment?: false
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Publication
21397064 | -
First Author: Harbuz R
Year: 2011
Journal: Am J Hum Genet
Title: A recurrent deletion of DPY19L2 causes infertility in man by blocking sperm head elongation and acrosome formation.
Volume: 88
Issue: 3
Pages: 351-61
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Publication
16526957 | -
 
First Author: Carson AR
Year: 2006
Journal: BMC Genomics
Title: Duplication and relocation of the functional DPY19L2 gene within low copy repeats.
Volume: 7
Pages: 45
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Publication
21397063 | -
First Author: Koscinski I
Year: 2011
Journal: Am J Hum Genet
Title: DPY19L2 deletion as a major cause of globozoospermia.
Volume: 88
Issue: 3
Pages: 344-50
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Protein Domain
IPR030042 | DPY19L2
Type: Family
Description: Dpy-19-like proteins (DPY19L) constitute a novel transmembrane protein family []. This entry represents DPY19L2. DPY19L2 deletion is a major cause of globozoospermia, a condition characterised by round-headed spermatozoa which results in infertility [, ]. DPY19L2 originated from an initial duplication of DPY19L1 on chromosome 7, followed by a recent relocalisation on chromosome 12 in humans, leaving the initial copy on chromosome 7 as a pseudogene (DPY19L2P1) [].
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Protein
P0CW70
Organism: Mus musculus/domesticus
Length: 773  
Fragment?: false
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Publication
15489334 | -
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
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Publication
21183079 | J:292518
First Author: Huttlin EL
Year: 2010
Journal: Cell
Title: A tissue-specific atlas of mouse protein phosphorylation and expression.
Volume: 143
Issue: 7
Pages: 1174-89
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Publication
19468303 | -
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
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