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COG4 gene

Known as: DKFZP586E1519, COMPONENT OF OLIGOMERIC GOLGI COMPLEX 4, COD1 
National Institutes of Health

Related topics

Related topics

1 relation
COG4 protein, S cerevisiae

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
A Recurrent De Novo Heterozygous COG4 Substitution Leads to Saul-Wilson Syndrome, Disrupted Vesicular Trafficking, and Altered Proteoglycan Glycosylation.
The conserved oligomeric Golgi (COG) complex is involved in intracellular vesicular transport, and is composed of eight subunits… Expand
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2015
2015
Mutations in COG2 encoding a subunit of the conserved oligomeric golgi complex cause a congenital disorder of glycosylation
The conserved oligomeric Golgi (COG) complex is involved in intra‐Golgi retrograde trafficking, and mutations in six of its eight… Expand
2014
2014
Multipronged interaction of the COG complex with intracellular membranes
The conserved oligomeric Golgi complex is a peripheral membrane protein complex that orchestrates the tethering and fusion of… Expand
2011
2011
Identification of the first COG-CDG patient of Indian origin.
Mutations in the Conserved Oligomeric Golgi (COG) complex give rise to type II congenital disorders of glycosylation (CDG). Thus… Expand
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Highly Cited
2009
Highly Cited
2009
Structural basis for a human glycosylation disorder caused by mutation of the COG4 gene
The proper glycosylation of proteins trafficking through the Golgi apparatus depends upon the conserved oligomeric Golgi (COG… Expand
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Highly Cited
2009
Highly Cited
2009
Golgi function and dysfunction in the first COG4-deficient CDG type II patient
The conserved oligomeric Golgi (COG) complex is a hetero-octameric complex essential for normal glycosylation and intra-Golgi… Expand
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Highly Cited
2009
Highly Cited
2009
Deficiency in COG5 causes a moderate form of congenital disorders of glycosylation.
The conserved oligomeric Golgi (COG) complex is a tethering factor composed of eight subunits that is involved in the retrograde… Expand
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Highly Cited
2002
Highly Cited
2002
Cod1p/Spf1p is a P-type ATPase involved in ER function and Ca2+ homeostasis
The internal environment of the ER is regulated to accommodate essential cellular processes, yet our understanding of this… Expand
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1998
1998
Linkage analysis of X-linked cone-rod dystrophy: localization to Xp11.4 and definition of a locus distinct from RP2 and RP3.
Progressive X-linked cone-rod dystrophy (COD1) is a retinal disease affecting primarily the cone photoreceptors. The COD1 locus… Expand
1994
1994
Clinical diversity and chromosomal localization of X-linked cone dystrophy (COD1).
X-linked progressive cone dystrophy (COD1) causes progressive deterioration of visual acuity, deepening of central scotomas… Expand
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