Gene Gene information from NCBI Gene database.
Entrez ID 5245
Gene name Prohibitin 1
Gene symbol PHB1
Synonyms (NCBI Gene)
BAP32HEL-215HEL-S-54ePHB
Chromosome 17
Chromosome location 17q21.33
SNPs SNP information provided by dbSNP.
1
SNP ID Visualize variation Clinical significance Consequence
rs112294663 G>A,C,T Risk-factor 3 prime UTR variant
miRNA miRNA information provided by mirtarbase database.
428
miRTarBase ID miRNA Experiments Reference
MIRT001210 hsa-miR-27a-3p qRT-PCRGFP reporter assayWestern blot 18789835
MIRT001210 hsa-miR-27a-3p qRT-PCRGFP reporter assayWestern blot 18789835
MIRT001210 hsa-miR-27a-3p ChIP-seqLuciferase reporter assayNorthern blotqRT-PCRWestern blot 22505583
MIRT001210 hsa-miR-27a-3p ChIP-seqLuciferase reporter assayNorthern blotqRT-PCRWestern blot 22505583
MIRT001210 hsa-miR-27a-3p ChIP-seqLuciferase reporter assayNorthern blotqRT-PCRWestern blot 22505583
Transcription factors Transcription factors information provided by TRRUST V2 database.
4
Transcription factor Regulation Reference
HDAC1 Repression 21152868
HDAC2 Repression 21152868
STAT3 Unknown 17324931
VDR Unknown 16849588;17207617
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
85
GO ID Ontology Definition Evidence Reference
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IDA 16964284
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IEA
GO:0001649 Process Osteoblast differentiation HDA 16210410
GO:0001850 Function Complement component C3a binding IDA 17070910
GO:0001851 Function Complement component C3b binding IDA 17070910
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
176705 8912 ENSG00000167085
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P35232
Protein name Prohibitin 1
Protein function Protein with pleiotropic attributes mediated in a cell-compartment- and tissue-specific manner, which include the plasma membrane-associated cell signaling functions, mitochondrial chaperone, and transcriptional co-regulator of transcription fac
PDB 8RRH
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01145 Band_7 28 210 SPFH domain / Band 7 family Family
Tissue specificity TISSUE SPECIFICITY: Widely expressed in different tissues.
Sequence
Sequence length 272
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Virion - Flavivirus and Alphavirus   RAF activation
Signaling by moderate kinase activity BRAF mutants
Paradoxical activation of RAF signaling by kinase inactive BRAF
Processing of SMDT1
Signaling downstream of RAS mutants
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
9
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Acute myeloid leukemia Benign rs2277637 RCV005937118
Breast cancer, susceptibility to risk factor rs112294663 RCV000014325
Familial cancer of breast Benign rs2233667 RCV005918614
Hepatocellular carcinoma Benign rs2233667 RCV005918615