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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

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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
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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
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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
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
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
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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2002
2002
Cod 1 p / Spf 1 p is a P-type ATPase involved in ER function and Ca 2 homeostasis
he 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
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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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