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component of oligomeric golgi complex 7

Summary

Gene Symbol

COG7

Organism

Homo sapiens (human)

External Links

NCBI Gene

91949

HGNC

18622

KEGG Gene ID

hsa:91949

PubChem

91949

Alliance of Genome Resources

HGNC:18622

Annotation

Keyword

Coiled coil
Congenital disorder of glycosylation
Golgi apparatus
Membrane
Protein transport
Reference proteome

Proteins

Displaying **all 2** entries
UniProt	Protein Name
P83436	Component of oligomeric Golgi complex 7
A0A0S2Z652	Component of oligomeric Golgi complex 7

Annotation information from UniProt.

Gene Ontology (GO)

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GO Term	Evidence Code	PMID
Golgi organization	IBA IMP	27066481
protein localization to organelle	IMP	16420527
protein stabilization	IMP	16420527 16510524
intracellular protein transport	IMP	15107842
retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum	IBA IMP	16420527 16510524

GO Hierarchy

biological process

metabolic process [inference]

nitrogen compound metabolic process [inference]

organonitrogen compound metabolic process [inference]

protein metabolic process [inference]

protein modification process [inference]

protein glycosylation

primary metabolic process [inference]

protein metabolic process [inference]

protein modification process [inference]

protein glycosylation

glycosylation

macromolecule glycosylation [inference]

protein glycosylation

organic substance metabolic process [inference]

macromolecule metabolic process [inference]

protein metabolic process [inference]

protein modification process [inference]

protein glycosylation

macromolecule modification [inference]

protein modification process [inference]

protein glycosylation

macromolecule glycosylation [inference]

protein glycosylation

organonitrogen compound metabolic process [inference]

protein metabolic process [inference]

protein modification process [inference]

protein glycosylation

cellular process [inference]

vesicle-mediated transport [inference]

Golgi vesicle transport [inference]

retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum

intra-Golgi vesicle-mediated transport [inference]

retrograde transport, vesicle recycling within Golgi

cellular localization [inference]

intracellular transport [inference]

intracellular protein transport

cellular macromolecule localization [inference]

protein localization [inference]

protein localization to organelle

protein localization to Golgi apparatus

establishment of protein localization [inference]

protein transport [inference]

intracellular protein transport

cellular component organization or biogenesis [inference]

cellular component organization [inference]

organelle organization [inference]

Golgi organization

localization [inference]

macromolecule localization [inference]

cellular macromolecule localization [inference]

protein localization [inference]

protein localization to organelle

protein localization to Golgi apparatus

establishment of protein localization [inference]

protein transport [inference]

intracellular protein transport

establishment of localization [inference]

transport [inference]

vesicle-mediated transport [inference]

Golgi vesicle transport [inference]

retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum

intra-Golgi vesicle-mediated transport [inference]

retrograde transport, vesicle recycling within Golgi

intracellular transport [inference]

intracellular protein transport

organic substance transport [inference]

protein transport [inference]

intracellular protein transport

nitrogen compound transport [inference]

protein transport [inference]

intracellular protein transport

establishment of protein localization [inference]

protein transport [inference]

intracellular protein transport

establishment of localization in cell [inference]

intracellular transport [inference]

intracellular protein transport

cellular localization [inference]

intracellular transport [inference]

intracellular protein transport

cellular macromolecule localization [inference]

protein localization [inference]

protein localization to organelle

protein localization to Golgi apparatus

establishment of protein localization [inference]

protein transport [inference]

intracellular protein transport

biological regulation [inference]

regulation of biological quality [inference]

regulation of protein stability [inference]

protein stabilization

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GO Term	Evidence Code	PMID
intracellular membrane-bounded organelle	IDA
trans-Golgi network membrane
Golgi apparatus	IDA	11980916
Golgi membrane	NAS	27066481
nucleolus	IDA

GO Hierarchy

cellular component

protein-containing complex [inference]

vesicle tethering complex [inference]

Golgi transport complex

cellular anatomical entity [inference]

membrane [inference]

organelle membrane [inference]

trans-Golgi network membrane

bounding membrane of organelle [inference]

Golgi membrane

organelle [inference]

membrane-bounded organelle [inference]

intracellular membrane-bounded organelle

Golgi apparatus

non-membrane-bounded organelle [inference]

intracellular non-membrane-bounded organelle [inference]

nucleolus

intracellular organelle [inference]

intracellular membrane-bounded organelle

Golgi apparatus

intracellular non-membrane-bounded organelle [inference]

nucleolus

Displaying 1 entry
GO Term	Evidence Code	PMID
protein binding	IPI	15047703 19536132 21903422 25416956 26871637 31515488 32296183

GO Hierarchy

molecular function

binding [inference]

protein binding

Gene Ontology information from NCBI Gene and UniProt.

Human Protein Atlas

ENSG00000168434

Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.

Data available from v23.0.proteinatlas.org. Image credit: Human Protein Atlas

KEGG BRITE Database

Orthology

K20294

Name

conserved oligomeric Golgi complex subunit 7

References

11929878

Disease

Disease Ontology

Displaying entries **1 - 10** of 37 in total

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DO ID	Disease Name	Source
DOID:0050571	congenital disorder of glycosylation type II	DisGeNET
DOID:0050700	cardiomyopathy	DisGeNET
DOID:0060655	autosomal recessive congenital ichthyosis	DisGeNET
DOID:0060656	autosomal recessive congenital ichthyosis 1	DisGeNET
DOID:0060710	autosomal recessive congenital ichthyosis 2	DisGeNET
DOID:0060711	autosomal recessive congenital ichthyosis 3	DisGeNET
DOID:0060712	autosomal recessive congenital ichthyosis 4A	DisGeNET
DOID:0060714	autosomal recessive congenital ichthyosis 5	DisGeNET
DOID:0060715	autosomal recessive congenital ichthyosis 6	DisGeNET
DOID:0060716	autosomal recessive congenital ichthyosis 7	DisGeNET

The Human Phenotype Ontology

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HPO ID	HPO Term
HP:0000007	Autosomal recessive inheritance
HP:0000011	Neurogenic bladder
HP:0000077	Abnormality of the kidney
HP:0000126	Hydronephrosis
HP:0000160	Narrow mouth
HP:0000253	Progressive microcephaly
HP:0000278	Retrognathia
HP:0000294	Low anterior hairline
HP:0000319	Smooth philtrum
HP:0000341	Narrow forehead

Displaying **all 2** entries
Disease ID	Disease Name
OMIM:608779	COG7-congenital disorder of glycosylation
ORPHA:79333	COG7-congenital disorder of glycosylation

PubChem Disease

MedGen Diseases

COG7 congenital disorder of glycosylation

OMIM Phenotypes

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIe; CDG2E

KEGG Diseases

Congenital disorders of glycosylation type II

Gene-Disease-Co-Occurrences-in-Literature (PubChem)

Ortholog

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Species	Gene ID	Alliance of Genome Resources	Orthologous MAtrix
Drosophila melanogaster	43547	FB:FBgn0051040
Ciona intestinalis	100185334		CIOIN00669
Callorhinchus milii	103186628		CALMI35121
Latimeria chalumnae	102353663		LATCH08542
Danio rerio	768247	ZFIN:ZDB-GENE-061013-463	DANRE26625
Ictalurus punctatus	108264483		ICTPU13354
Electrophorus electricus	113578455		ELEEL22304
Salmo salar	106578298		SALSA91040
Salmo salar	106579184		SALSA93280
Salmo trutta	115160107		SALTR01235

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

Summary

External Links

Annotation

KEGG BRITE Database

PubChem Disease

International Collaboration

Acknowledgements