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COG1

COG1

Protein-coding gene in the species Homo sapiens

protein that in humans is encoded by the COG1 gene. The protein encoded by this gene is one of eight proteins (Cog1-8) which form a Golgi-localized complex

COG1

Exophthalmos

Bulging of the eye anteriorly out of the orbit

Chondrodysplasia with joint dislocations, gPAPP type Cloverleaf skull syndrome COG1 congenital disorder of glycosylation Cole-Carpenter syndrome 1, 2 Congenital

Exophthalmos

Micrognathism

Condition in which the jaw is small

dislocations, gPAPP type Cleidocranial dysostosis Coffin–Siris syndrome 6 and 12 COG1 congenital disorder of glycosylation COG7 congenital disorder of glycosylation

Micrognathism

Microtia

Birth defect that affects the ears

Branchiootorenal syndrome 1 CHARGE association Chromosome 1p36 deletion syndrome COG1 congenital disorder of glycosylation Complete trisomy 21 syndrome Diamond-Blackfan

Microtia

Coggeshall

Village in Essex, England

3 times a day to Kelvedon station from 1982 – Coggeshall Community Bus (COG1) – Weekday (Monday-Friday) peak hours service from the town to Kelvedon station

Coggeshall

Conserved oligomeric Golgi complex

lipid binding domain. The first lobe of the COG complex contains subunits Cog1-Cog4 and the second lobe contains subunits Cog5-Cog8 . The lobes are connected

Conserved oligomeric Golgi complex

Conserved_oligomeric_Golgi_complex

Congenital disorder of glycosylation

Medical condition

(COG7-CDG) 608779 COG7 16p IIf (SLC35A1-CDG) 603585 SLC35A1 6q15 IIg (COG1-CDG) 611209 COG1 17q25.1 IIh (COG8-CDG) 611182 COG8 16q22.1 IIi (COG5-CDG) 613612

Congenital disorder of glycosylation

Congenital_disorder_of_glycosylation

Jasminne Mendez

American poet

original on June 30, 2020. Retrieved 2020-05-15. "Jasminne Mendez Issue 9". cog1. Archived from the original on 2020-07-01. Retrieved 2020-05-15. "Reclamation

Jasminne Mendez

Jasminne_Mendez

List of human protein-coding genes 2

HGNC:22199; O75128 3321 COBLL1 HGNC:23571; Q53SF7 3322 COCH HGNC:2180; O43405 3323 COG1 HGNC:6545; Q8WTW3 3324 COG2 HGNC:6546; Q14746 3325 COG3 HGNC:18619; Q96JB2

List of human protein-coding genes 2

List_of_human_protein-coding_genes_2

COG4

Protein-coding gene in the species Homo sapiens

2002).[supplied by OMIM] COG4 has been shown to interact with COG7, COG2, COG1 and COG5. Mutations in this gene have been associated with Saul-Wilson syndrome

COG4

COG3

Protein-coding gene in the species Homo sapiens

intra-Golgi transport vesicles. COG3 has been shown to interact with COG2 and COG1. GRCh38: Ensembl release 89: ENSG00000136152 – Ensembl, May 2017 GRCm38:

COG3

List of OMIM disorder codes

autosomal recessive; 603513; GAD1 Cerebrocostomandibular-like syndrome; 611209; COG1 Cerebrooculofacioskeletal syndrome 1; 214150; ERCC6 Cerebrooculofacioskeletal

List of OMIM disorder codes

List_of_OMIM_disorder_codes