Gene Gene information from NCBI Gene database.
Entrez ID 2342
Gene name Farnesyltransferase, CAAX box, subunit beta
Gene symbol FNTB
Synonyms (NCBI Gene)
FPTB
Chromosome 14
Chromosome location 14q23.3
miRNA miRNA information provided by mirtarbase database.
236
miRTarBase ID miRNA Experiments Reference
MIRT004223 hsa-miR-346 Microarray 16822819
MIRT030444 hsa-miR-24-3p Microarray 19748357
MIRT047154 hsa-miR-183-5p CLASH 23622248
MIRT1000903 hsa-miR-1304 CLIP-seq
MIRT1000904 hsa-miR-1321 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
24
GO ID Ontology Definition Evidence Reference
GO:0003824 Function Catalytic activity IEA
GO:0004659 Function Prenyltransferase activity IEA
GO:0004660 Function Protein farnesyltransferase activity IBA
GO:0004660 Function Protein farnesyltransferase activity IDA 19228685
GO:0004660 Function Protein farnesyltransferase activity IDA 16893176
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
134636 3785 ENSG00000257365
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Terpenoid backbone biosynthesis   Inactivation, recovery and regulation of the phototransduction cascade
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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)
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
ANXIETY DISORDERS Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations