Gene Gene information from NCBI Gene database.
Entrez ID 11243
Gene name Polyamine modulated factor 1
Gene symbol PMF1
Synonyms (NCBI Gene)
-
Chromosome 1
Chromosome location 1q22
miRNA miRNA information provided by mirtarbase database.
96
miRTarBase ID miRNA Experiments Reference
MIRT024714 hsa-miR-215-5p Microarray 19074876
MIRT029956 hsa-miR-26b-5p Microarray 19088304
MIRT032379 hsa-let-7b-5p Proteomics 18668040
MIRT2299378 hsa-let-7a CLIP-seq
MIRT2299379 hsa-let-7b CLIP-seq
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:0000444 Component MIS12/MIND type complex IBA
GO:0000444 Component MIS12/MIND type complex IDA 16585270, 20819937, 27881301
GO:0000444 Component MIS12/MIND type complex IEA
GO:0000444 Component MIS12/MIND type complex NAS 21633384
GO:0000775 Component Chromosome, centromeric region IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
609176 9112 ENSG00000160783
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal
Separation of Sister Chromatids
Resolution of Sister Chromatid Cohesion
RHO GTPases Activate Formins
Mitotic Prometaphase
EML4 and NUDC in mitotic spindle formation
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
7
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
BREAST CANCER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CLEAR CELL RENAL CARCINOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
INTRACEREBRAL HEMORRHAGE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
KIDNEY CANCER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Cerebral Hemorrhage Associate 37787451
★☆☆☆☆
Found in Text Mining only
Cerebral Small Vessel Diseases Associate 31430377
★☆☆☆☆
Found in Text Mining only
COVID 19 Associate 37794074
★☆☆☆☆
Found in Text Mining only
Stroke Associate 36958462
★★☆☆☆
Found in Text Mining + Unknown/Other Associations