GOLGA8A

Last updated
GOLGA8A
Identifiers
Aliases GOLGA8A , GM88, golgin A8 family member A
External IDs HomoloGene: 121673 GeneCards: GOLGA8A
Gene location (Human)
Ideogram human chromosome 15.svg
Chr. Chromosome 15 (human) [1]
Human chromosome 15 ideogram.svg
HSR 1996 II 3.5e.svg
Red rectangle 2x18.png
Band 15q14Start34,379,068 bp [1]
End34,437,466 bp [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_181077

n/a

RefSeq (protein)

NP_851422

n/a

Location (UCSC) Chr 15: 34.38 – 34.44 Mb n/a
PubMed search [2] n/a
Wikidata
View/Edit Human

Golgin A8 family member A is a protein that in humans is encoded by the GOLGA8A gene. [3]

Protein biological molecule consisting of chains of amino acid residues

Proteins are large biomolecules, or macromolecules, consisting of one or more long chains of amino acid residues. Proteins perform a vast array of functions within organisms, including catalysing metabolic reactions, DNA replication, responding to stimuli, providing structure to cells and organisms, and transporting molecules from one location to another. Proteins differ from one another primarily in their sequence of amino acids, which is dictated by the nucleotide sequence of their genes, and which usually results in protein folding into a specific three-dimensional structure that determines its activity.

Gene basic physical and functional unit of heredity

In biology, a gene is a sequence of nucleotides in DNA or RNA that codes for a molecule that has a function. During gene expression, the DNA is first copied into RNA. The RNA can be directly functional or be the intermediate template for a protein that performs a function. The transmission of genes to an organism's offspring is the basis of the inheritance of phenotypic trait. These genes make up different DNA sequences called genotypes. Genotypes along with environmental and developmental factors determine what the phenotypes will be. Most biological traits are under the influence of polygenes as well as gene–environment interactions. Some genetic traits are instantly visible, such as eye color or number of limbs, and some are not, such as blood type, risk for specific diseases, or the thousands of basic biochemical processes that constitute life.

Contents

Function

The Golgi apparatus, which participates in glycosylation and transport of proteins and lipids in the secretory pathway, consists of a series of stacked, flattened membrane sacs referred to as cisternae. Interactions between the Golgi and microtubules are thought to be important for the reorganization of the Golgi after it fragments during mitosis. The golgins constitute a family of proteins which are localized to the Golgi. This gene encodes a golgin which structurally resembles its family member GOLGA2, suggesting that they may share a similar function. There are many similar copies of this gene on chromosome 15. Alternative splicing results in multiple transcript variants.

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GOLGA2 protein-coding gene in the species Homo sapiens

Golgin subfamily A member 2 is a protein that in humans is encoded by the GOLGA2 gene.

USO1 protein-coding gene in the species Homo sapiens

General vesicular transport factor p115 is a protein that in humans is encoded by the USO1 gene.

RAB1A protein-coding gene in the species Homo sapiens

Ras-related protein Rab-1A is a protein that in humans is encoded by the RAB1A gene.

GOLGA3 protein-coding gene in the species Homo sapiens

Golgin subfamily A member 3 is a protein that in humans is encoded by the GOLGA3 gene.

GOLGA4 protein-coding gene in the species Homo sapiens

Golgin subfamily A member 4 is a protein that in humans is encoded by the GOLGA4 gene.

ARL1 protein-coding gene in the species Homo sapiens

ADP-ribosylation factor-like protein 1 is a protein that in humans is encoded by the ARL1 gene.

GOLGA5 protein-coding gene in the species Homo sapiens

Golgin subfamily A member 5 is a protein that in humans is encoded by the GOLGA5 gene.

BLZF1 protein-coding gene in the species Homo sapiens

Golgin-45 is a protein that in humans is encoded by the BLZF1 gene.

GCC2 protein-coding gene in the species Homo sapiens

GRIP and coiled-coil domain-containing protein 2 is a protein that in humans is encoded by the GCC2 gene.

ACBD3 protein-coding gene in the species Homo sapiens

Golgi resident protein GCP60 is a protein that in humans is encoded by the ACBD3 gene.

GOLGA1 protein-coding gene in the species Homo sapiens

Golgin subfamily A member 1 is a protein that in humans is encoded by the GOLGA1 gene.

GCC1 protein-coding gene in the species Homo sapiens

GRIP and coiled-coil domain-containing protein 1 is a protein that in humans is encoded by the GCC1 gene.

GORAB protein-coding gene in the species Homo sapiens

RAB6-interacting golgin also known as N-terminal kinase-like-binding protein 1 (NTKL-BP1) or SCY1-like 1-binding protein 1 (SCYL1-BP1) is a protein that in humans is encoded by the GORAB gene.

Inositol monophosphatase 3 protein-coding gene in the species Homo sapiens

Inositol monophosphatase 3 also known as inositol monophosphatase domain-containing protein 1 (IMPAD1) is an enzyme that in humans is encoded by the IMPAD1 gene.

Giantin protein-coding gene in the species Homo sapiens

Giantin or Golgin subfamily B member 1 is a protein that in humans is encoded by the GOLGB1 gene. Giantin is a disulfide-linked homodimer.

Golgi matrix

The Golgi matrix is a collection of proteins involved in the structure and function of the Golgi apparatus. The matrix was first isolated in 1994 as an amorphous collection of 12 proteins that remained associated together in the presence of detergent and 150 mM NaCl. Treatment with a protease enzyme removed the matrix, which confirmed the importance of proteins for the matrix structure. Modern freeze etch electron microscopy (EM) clearly shows a mesh connecting Golgi cisternae and associated vesicles. Further support for the existence of a matrix comes from EM images showing that ribosomes are excluded from regions between and near Golgi cisternae.

Golgin a7 protein-coding gene in the species Homo sapiens

Golgin A7 is a protein that in humans is encoded by the GOLGA7 gene.

GOLGA8B protein-coding gene in the species Homo sapiens

Golgin A8 family member B is a protein that in humans is encoded by the GOLGA8B gene.

JAKMIP2 protein-coding gene in the species Homo sapiens

Janus kinase and microtubule interacting protein 2 is a protein that in humans is encoded by the JAKMIP2 gene.

References

Further reading


This article incorporates text from the United States National Library of Medicine, which is in the public domain.

United States National Library of Medicine the worlds largest medical library, operated by the US federal government

The United States National Library of Medicine (NLM), operated by the United States federal government, is the world's largest medical library.

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