CCPG1 - cell cycle progression 1 Gene

Homo sapiens

Also known as CPR8

Gene ID: 9236 | Gene type: protein coding

About CCPG1

Cytogenetic location: 15q21.3 Genomic coordinates (GRCh38): 15:55,355,239-55,408,359 (from NCBI)

This gene has 13 transcripts (splice variants) and 133 orthologues. Ubiquitous expression in thyroid (RPKM 34.7), gall bladder (RPKM 22.2) and 25 other tissues.

Summary

Involved in positive regulation of cell cycle and positive regulation of cell population proliferation. Predicted to be integral component of membrane. Predicted to be active in membrane. [provided by Alliance of Genome Resources, Apr 2022]

CCPG1 Products(4)

mRNA	Protein	Name
NM_001204450.2	NP_001191379.1	cell cycle progression protein 1 isoform 2
NM_001204451.2	NP_001191380.1	cell cycle progression protein 1 isoform 3
NM_004748.6	NP_004739.3	cell cycle progression protein 1 isoform 1
NM_020739.5	NP_065790.2	cell cycle progression protein 1 isoform 1

Protein Preferred Names

Protein Names

cell cycle progression protein 1

cell cycle progression restoration protein 8

Related Diseases

Diseases

Alias

Developmental And Epileptic Encephalopathy 80

DEE80	Glycosylphosphatidylinositol Biosynthesis Defect 20
Gpibd20	Epileptic Encephalopathy, Early Infantile, 80
Eiee80	Developmental And Epileptic Encephalopathy, 80
Early Infantile Epileptic Encephalopathy 80

Hereditary Sensory And Autonomic Neuropathy Type 1

Hereditary Sensory And Autonomic Neuropathy Type I	Hereditary Sensory Neuropathy-Deafness-Dementia Syndrome
Hsan1e	Hsan1
Dnmt1-Related Dementia, Deafness, And Sensory Neuropathy	Hsn1e
Hsnie	Hereditary Sensory Neuropathy Type Ie
Hereditary Sensory Neuropathy-Sensorineural Hearing Loss-Dementia Syndrome	Hereditary Sensory And Autonomic Neuropathy Type Ie
Hereditary Sensory And Autonomic Neuropathy Type 1e	Hereditary Sensory Neuropathy With Hearing Loss And Dementia
Dnmt1-Complex Disorder	Hereditary Sensory And Autonomic Neuropathy Type 1 With Dementia And Hearing Loss
Hsn Ie	Hereditary Sensory Autonomic Neuropathy, Type 1
Hsan1- [Hereditary Sensory And Autonomic Neuropathy Type I]

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-RS02146	CCPG1 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Canis familiaris	CCPG1	VGNC	VGNC:38910
Bos taurus	CCPG1	VGNC	VGNC:26982
Felis catus	CCPG1	VGNC	VGNC:60571
Rattus norvegicus	CCPG1	RGD	RGD:1311261
Mus musculus	CCPG1	MGD	MGI:1196419
Macaca mulatta	CCPG1	VGNC	VGNC:70844

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