COG7 - component of oligomeric golgi complex 7 Gene

Homo sapiens

Also known as CDG2E

Gene ID: 91949 | Gene type: protein coding

About COG7

Cytogenetic location: 16p12.2 Genomic coordinates (GRCh38): 16:23,388,493-23,453,189 (from NCBI)

This gene has 6 transcripts (splice variants), 209 orthologues and is associated with 3 phenotypes. Ubiquitous expression in thyroid (RPKM 7.2), prostate (RPKM 6.0) and 25 other tissues.

Summary

The protein encoded by this gene resides in the golgi, and constitutes one of the 8 subunits of the conserved oligomeric Golgi (COG) complex, which is required for normal golgi morphology and localization. Mutations in this gene are associated with the congenital disorder of glycosylation type IIe.[provided by RefSeq, May 2010]

COG7 Products(1)

mRNA	Protein	Name
NM_153603.4	NP_705831.1	conserved oligomeric Golgi complex subunit 7

Gene Ontology

Molecular Function
Biological Process
Cellular Component

Molecular Function GO Annotation	Evidence	Reference	Source
enables protein binding	IPI IPI: Inferred from physical interaction	15047703	GOA

Biological Process GO Annotation	Evidence	Reference	Source
involved in Golgi organization	IMP IMP: Inferred from mutant phenotype	27066481	GOA
involved in glycosylation	IMP IMP: Inferred from mutant phenotype	27066481	GOA
involved in intracellular protein transport	IMP IMP: Inferred from mutant phenotype	15107842	GOA
involved in protein glycosylation	IMP IMP: Inferred from mutant phenotype	15107842	GOA
involved in protein localization to Golgi apparatus	IMP IMP: Inferred from mutant phenotype	16510524	GOA
involved in protein localization to organelle	IMP IMP: Inferred from mutant phenotype	16420527	GOA
involved in protein stabilization	IMP IMP: Inferred from mutant phenotype	16420527	GOA
involved in retrograde transport, vesicle recycling within Golgi	IMP IMP: Inferred from mutant phenotype	27066481	GOA
involved in retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum	IMP IMP: Inferred from mutant phenotype	16420527	GOA

Cellular Component GO Annotation	Evidence	Reference	Source
located in Golgi apparatus	IDA IDA: Inferred from direct assay	11980916	GOA
part of Golgi transport complex	IDA IDA: Inferred from direct assay	15047703	GOA

EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

COG7 Protein Structure

COG7

0
200
400
600
770 a.a.

Protein Preferred Names

Protein Names

conserved oligomeric Golgi complex subunit 7

COG complex subunit 7

COG7 Protein-protein interaction Information

Type Cross Intra	Protein Name	Protein ID	Interactor	Interactor Species	Interactor ID	Detection Method	Reference
Intra	COG7	P83436	KIFC3	Homo sapiens	Q9BVG8-5	Y2H Array	32296183
Intra	COG7	P83436	KIFC3	Homo sapiens	Q9BVG8-5	Y2H Prey Pooling	26871637
Intra	COG7	P83436	KIFC3	Homo sapiens	Q9BVG8-5	Y2H Prey Pooling	32296183
Intra	COG7	P83436	KIFC3	Homo sapiens	Q9BVG8-5	Validated Y2H	26871637
Intra	COG7	P83436	KIFC3	Homo sapiens	Q9BVG8-5	Validated Y2H	32296183
Intra	COG7	P83436	KIFC3	Homo sapiens	Q9BVG8-5	Y2H Array	26871637
Intra	COG7	P83436	MEOX2	Homo sapiens	Q6FHY5	Y2H Array	26871637
Intra	COG7	P83436	MEOX2	Homo sapiens	Q6FHY5	Y2H Prey Pooling	26871637
Intra	COG7	P83436	MEOX2	Homo sapiens	Q6FHY5	Validated Y2H	26871637
Intra	COG7	P83436	COG4	Homo sapiens	Q9H9E3	CoIP	15047703
Intra	COG7	P83436	COG4	Homo sapiens	Q9H9E3	Anti Bait CoIP	19536132
Intra	COG7	P83436	COG4	Homo sapiens	Q9H9E3	Anti Tag CoIP	33961781
Intra	COG7	P83436	COG5	Homo sapiens	Q9UP83	CoIP	15047703
Intra	COG7	P83436	COG5	Homo sapiens	Q9UP83	Anti Tag CoIP	33961781
Intra	COG7	P83436	TAX1BP1	Homo sapiens	Q86VP1	Y2H Array	32296183
Intra	COG7	P83436	TAX1BP1	Homo sapiens	Q86VP1	Validated Y2H	26871637
Intra	COG7	P83436	TAX1BP1	Homo sapiens	Q86VP1	Y2H Array	26871637
Intra	COG7	P83436	TAX1BP1	Homo sapiens	Q86VP1	Validated Y2H	25416956
Intra	COG7	P83436	TAX1BP1	Homo sapiens	Q86VP1	Validated Y2H	32296183
Intra	COG7	P83436	TAX1BP1	Homo sapiens	Q86VP1	Y2H Prey Pooling	26871637
Intra	COG7	P83436	TAX1BP1	Homo sapiens	Q86VP1	Y2H Prey Pooling	32296183

Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases

Alias

Immunodeficiency 47

Congenital Disorder Of Glycosylation Type Ii	CDG2E
Congenital Disorder Of Glycosylation Type Iie	IMD47
Cdg2s	Cdg Iis
Cdgiis	Immunodeficiency And Hepatopathy With Or Without Neurologic Features
Congenital Disorder Of Glycosylation, Type Ii	CDG1I
Congenital Disorder Of Glycosylation, Type Iie	Cdg Iie
Congenital Disorder Of Glycosylation Type 2e	Congenital Disorder Of Glycosylation, Type Iis
Cdg Ii	Cdgii
Cdgiie	Carbohydrate Deficient Glycoprotein Syndrome Type Iie
Cdg Syndrome Type Iie	Congenital Disorder Of Glycosylation Ii
Congenital Disorder Of Glycosylation 1i	Cdg-Iie
Alg2-Cdg	Cdg-Ii
Glycosylation, Congenital Disorder Of, Type Ii	Cdgiide
Congenital Disorder Of Glycosylation Type Iis	Cog7-Cdg
Cdg Syndrome Type Ii	Carbohydrate Deficient Glycoprotein Syndrome Type Ii
Congenital Disorder Of Glycosylation Type 1i	Mannosyltransferase 2 Deficiency
Congenital Disorder Of Glycosylation 2e	Congenital Disorder Of Glycosylation 2s
Congenital Disorders Of Glycosylation Type Ii	Glycosylation, Congenital Disorder Of, Type Iie
Immunodeficiency, Type 47	Congenital Disorder Of Glycosylation Type 2a

Congenital Disorder Of Glycosylation, Type Iih

CDG2H	Congenital Disorder Of Glycosylation Type Iih
Cdg Iih	Cdgiih
Carbohydrate Deficient Glycoprotein Syndrome Type Iih	Congenital Disorder Of Glycosylation Type 2h
Cog8-Cdg	Cdg-Iih
Cdgiidh	Cdg Syndrome Type Iih
Congenital Disorder Of Glycosylation 2h	Glycosylation, Congenital Disorder Of, Type Iih

Congenital Disorder Of Glycosylation, Type Iij

CDG2J	Congenital Disorder Of Glycosylation Type Iij
Cdg Iij	Cdgiij
Carbohydrate Deficient Glycoprotein Syndrome Type Iij	Cdg Syndrome Type Iij
Congenital Disorder Of Glycosylation Type 2j	Cog4-Cdg
Cdg-Iij	Cdgiidj
Congenital Disorder Of Glycosylation 2j	Glycosylation, Congenital Disorder Of, Type Iij

Congenital Disorder Of Glycosylation, Type Iii

CDG2I	Congenital Disorder Of Glycosylation Type Iii
Cdgiii	Carbohydrate Deficient Glycoprotein Syndrome Type Iii
Congenital Disorder Of Glycosylation Type 2i	Cog5-Cdg
Cdgiidi	Congenital Disorder Of Glycosylation 2i
Glycosylation, Congenital Disorder Of, Type Iii	Congenital Disorder Of Glycosylation, Type I-Iix

Congenital Disorder Of Glycosylation, Type Iil

CDG2L	Congenital Disorder Of Glycosylation Type Iil
Cdg Iil	Cog6-Cgd
Cdgiil	Cdg Syndrome Type Iil
Congenital Disorder Of Glycosylation Type 2l	Cdg-Iil
Cdgiidl	Congenital Disorder Of Glycosylation 2l
Glycosylation, Congenital Disorder Of, Type Iil

White-Sutton Syndrome

WHSUS	Mrd37
Intellectual Disability-Microcephaly-Strabismus-Behavioral Abnormalities Syndrome	Mental Retardation, Autosomal Dominant 37
Autosomal Dominant Mental Retardation 37	Pogz-Related Intellectual Disability Syndrome

Saul-Wilson Syndrome

Microcephalic Osteodysplastic Dysplasia	Microcephalic Osteodysplastic Dysplasia, Saul-Wilson Type
SWILS	Microcephalic Osteodysplastic Dysplasia Saul Wilson Type

Geroderma Osteodysplasticum

Gerodermia Osteodysplastica	Geroderma Osteodysplastica
GO	Walt Disney Dwarfism
Type Of Gerodermia Osteodysplastica

Congenital Disorder Of Glycosylation, Type In

Congenital Disorder Of Glycosylation	CDG1N
Congenital Disorders Of Glycosylation	Cdg In
Cdgin	Congenital Disorder Of Glycosylation 1n
Carbohydrate-Deficient Glycoprotein Syndrome	Cdg
Rft1-Cdg	Cdg-In
Congenital Disorder Of Glycosylation Type In	Carbohydrate Deficient Glycoprotein Syndrome
Cdg Syndrome	Congenital Disorder Of Glycosylation In
Carbohydrate-Deficient Glycoprotein Syndromes	Cdg Syndrome Type In
Carbohydrate Deficient Glycoprotein Syndrome Type In	Congenital Disorder Of Glycosylation Type 1n
Man5glcnac2-Pp-Dol Flippase Deficiency	Glycosylation, Congenital Disorder Of
Glycosylation, Congenital Disorder Of, Type In

Granulomatous Disease, Chronic, X-Linked

CGDX	Chronic Granulomatous Disease, X-Linked
X-Linked Chronic Granulomatous Disease	Cgd
Cytochrome B-Negative Granulomatous Disease, Chronic, X-Linked	Cdgx
X-Linked Chronic Cytochrome B-Negative Granulomatous Disease	Chronic Granulomatous Disease Cytochrome B-Negative X-Linked
Chronic Granulomatous Disease Cytochrome B-Positive X-Linked	Granulomatous Disease, Chronic, X-Linked, Variant

Microcephaly

Microencephaly	Microcephalus
Microcephalic	Nanocephaly
Congenital Microcephaly	Brain Hypoplasia
Brain Nondevelopment	Cephalic Hypoplasia
Undeveloped Cerebrum	Undeveloped Brain
Micrencephalon	Micrencephaly

Diseases	Alias
Waldenstroem'S Macroglobulinemia	Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS02956	COG7 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Mus musculus	COG7	MGD	MGI:2685013
Felis catus	COG7	VGNC	VGNC:61050
Rattus norvegicus	COG7	RGD	RGD:1566058
Macaca mulatta	COG7	VGNC	VGNC:71208
Bos taurus	COG7	VGNC	VGNC:27551
Canis familiaris	COG7	VGNC	VGNC:39453

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