Gene Gene information from NCBI Gene database.
Entrez ID 9453
Gene name Geranylgeranyl diphosphate synthase 1
Gene symbol GGPS1
Synonyms (NCBI Gene)
GGPPSGGPPS1MDHLOMUDHLOV
Chromosome 1
Chromosome location 1q42.3
Summary This gene is a member of the prenyltransferase family and encodes a protein with geranylgeranyl diphosphate (GGPP) synthase activity. The enzyme catalyzes the synthesis of GGPP from farnesyl diphosphate and isopentenyl diphosphate. GGPP is an important mo
miRNA miRNA information provided by mirtarbase database.
282
miRTarBase ID miRNA Experiments Reference
MIRT052559 hsa-let-7a-5p CLASH 23622248
MIRT052321 hsa-let-7b-5p CLASH 23622248
MIRT045310 hsa-miR-186-5p CLASH 23622248
MIRT039170 hsa-miR-769-5p CLASH 23622248
MIRT637817 hsa-miR-1228-3p HITS-CLIP 23824327
Transcription factors Transcription factors information provided by TRRUST V2 database.
1
Transcription factor Regulation Reference
EGR1 Unknown 21983072
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
28
GO ID Ontology Definition Evidence Reference
GO:0004161 Function Dimethylallyltranstransferase activity IEA
GO:0004311 Function Geranylgeranyl diphosphate synthase activity IBA
GO:0004311 Function Geranylgeranyl diphosphate synthase activity IDA 9741684, 10026212
GO:0004311 Function Geranylgeranyl diphosphate synthase activity IEA
GO:0004311 Function Geranylgeranyl diphosphate synthase activity IMP 32403198
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
606982 4249 ENSG00000152904
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O95749
Protein name Geranylgeranyl pyrophosphate synthase (GGPP synthase) (GGPPSase) (EC 2.5.1.-) ((2E,6E)-farnesyl diphosphate synthase) (Dimethylallyltranstransferase) (EC 2.5.1.1) (Farnesyl diphosphate synthase) (Farnesyltranstransferase) (EC 2.5.1.29) (Geranylgeranyl dip
Protein function Catalyzes the trans-addition of the three molecules of IPP onto DMAPP to form geranylgeranyl pyrophosphate, an important precursor of carotenoids and geranylated proteins.
PDB 2Q80 , 6C56 , 6C57 , 6G31 , 6G32 , 6R4V , 9CSL
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00348 polyprenyl_synt 9 251 Polyprenyl synthetase Domain
Tissue specificity TISSUE SPECIFICITY: Abundantly expressed in testis (PubMed:10026212, PubMed:9741684). Found in other tissues to a lower extent (PubMed:10026212, PubMed:9741684). Expressed in dermal fibroblast and skeletal muscle (PubMed:32403198). {ECO:0000269|PubMed:100
Sequence
Sequence length 300
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Terpenoid backbone biosynthesis
Metabolic pathways
  Cholesterol biosynthesis
Activation of gene expression by SREBF (SREBP)
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
11
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession Evidence Score
Muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome Pathogenic rs772582396, rs2103351693, rs2103351813 RCV001620124
RCV001620125
RCV001620128
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Myopathy with tubular aggregates Likely pathogenic rs2528261065 RCV004587625
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
Myopathy Uncertain significance; Conflicting classifications of pathogenicity ClinVar
Disgenet
★★★☆☆
Reported in Unknown/Other Associations (≥2 sources)
NEUROMUSCULAR DISEASES Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
PERRAULT SYNDROME TYPE 1 Disgenet, Orphanet
Disgenet, Orphanet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
PERRAULT SYNDROME TYPE 2 Orphanet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Adenocarcinoma of Lung Associate 29377583
★☆☆☆☆
Found in Text Mining only
Carbamoyl Phosphate Synthase I Deficiency Disease Inhibit 35869884
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Associate 24716791
★☆☆☆☆
Found in Text Mining only
Fibrosis Associate 24716791
★☆☆☆☆
Found in Text Mining only
Hearing Loss Associate 35869884
★☆☆☆☆
Found in Text Mining only
Hyperinsulinism Associate 24716791
★☆☆☆☆
Found in Text Mining only
Liver Neoplasms Associate 24716791
★☆☆☆☆
Found in Text Mining only
Lymphatic Metastasis Stimulate 29377583
★☆☆☆☆
Found in Text Mining only
Muscular Dystrophies Associate 35869884
★☆☆☆☆
Found in Text Mining only
Neoplasm Metastasis Associate 29377583
★☆☆☆☆
Found in Text Mining only