FNTA (farnesyltransferase, CAAX box, subunit alpha)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 2339 |
| Gene name | Farnesyltransferase, CAAX box, subunit alpha |
| Gene symbol | FNTA |
| Synonyms (NCBI Gene) |
FPTAPGGT1APTAR2
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| Chromosome | 8 |
| Chromosome location | 8p11.21 |
| Summary | Prenyltransferases can attach either a farnesyl group or a geranylgeranyl group in thioether linkage to the cysteine residue of proteins with a C-terminal CAAX box. CAAX geranylgeranyltransferase and CAAX farnesyltransferase are heterodimers that share th |
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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P49354 | ||||||||||||||||||||||||||||||
| Protein name | Protein farnesyltransferase/geranylgeranyltransferase type-1 subunit alpha (EC 2.5.1.58) (EC 2.5.1.59) (CAAX farnesyltransferase subunit alpha) (FTase-alpha) (Ras proteins prenyltransferase subunit alpha) (Type I protein geranyl-geranyltransferase subunit | ||||||||||||||||||||||||||||||
| Protein function | Essential subunit of both the farnesyltransferase and the geranylgeranyltransferase complex. Contributes to the transfer of a farnesyl or geranylgeranyl moiety from farnesyl or geranylgeranyl diphosphate to a cysteine at the fourth position from | ||||||||||||||||||||||||||||||
| PDB | 1JCQ , 1LD7 , 1LD8 , 1MZC , 1S63 , 1SA4 , 1TN6 , 2F0Y , 2H6F , 2H6G , 2H6H , 2H6I , 2IEJ , 3E37 | ||||||||||||||||||||||||||||||
| Family and domains |
Pfam
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| Sequence |
MAATEGVGEAAQGGEPGQPAQPPPQPHPPPPQQQHKEEMAAEAGEAVASPMDDGFVSLDS |
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| Sequence length | 379 | ||||||||||||||||||||||||||||||
| Interactions | View interactions | ||||||||||||||||||||||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
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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)
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Related Genes
Genes most often co-reported with FNTA across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to FNTA (see Related Genes above), that are NOT already directly curated for FNTA itself -- a lead worth checking, not a confirmed association.
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