Gene Details | GeDiPNet - Complete Gene Info, Disease Associations & Pathways

Gene Gene miRNA Gene ontology Other IDs Pathways Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.	11243
Gene name Gene Name - the full gene name approved by the HGNC.	Polyamine modulated factor 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.	PMF1
Synonyms (NCBI Gene) Gene synonyms aliases	-
Chromosome Chromosome number	1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.	1q22

Show/Hide all(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
MIRT2299380	hsa-let-7c	CLIP-seq
MIRT2299381	hsa-let-7d	CLIP-seq
MIRT2299382	hsa-let-7e	CLIP-seq
MIRT2299383	hsa-let-7f	CLIP-seq
MIRT2299384	hsa-let-7g	CLIP-seq
MIRT2299385	hsa-let-7i	CLIP-seq
MIRT2299386	hsa-miR-1269	CLIP-seq
MIRT2299387	hsa-miR-1269b	CLIP-seq
MIRT2299388	hsa-miR-1285	CLIP-seq
MIRT2299389	hsa-miR-1287	CLIP-seq
MIRT2299390	hsa-miR-1288	CLIP-seq
MIRT2299391	hsa-miR-140-3p	CLIP-seq
MIRT2299392	hsa-miR-1587	CLIP-seq
MIRT2299393	hsa-miR-185	CLIP-seq
MIRT2299394	hsa-miR-1972	CLIP-seq
MIRT2299395	hsa-miR-2110	CLIP-seq
MIRT2299396	hsa-miR-214	CLIP-seq
MIRT2299397	hsa-miR-2467-3p	CLIP-seq
MIRT2299398	hsa-miR-3125	CLIP-seq
MIRT2299399	hsa-miR-3134	CLIP-seq
MIRT2299400	hsa-miR-3135b	CLIP-seq
MIRT2299401	hsa-miR-3157-5p	CLIP-seq
MIRT2299402	hsa-miR-3180	CLIP-seq
MIRT2299403	hsa-miR-3180-3p	CLIP-seq
MIRT2299404	hsa-miR-3184	CLIP-seq
MIRT2299405	hsa-miR-3187-5p	CLIP-seq
MIRT2299406	hsa-miR-3196	CLIP-seq
MIRT2299407	hsa-miR-331-3p	CLIP-seq
MIRT2299408	hsa-miR-3619-3p	CLIP-seq
MIRT2299409	hsa-miR-3619-5p	CLIP-seq
MIRT2299410	hsa-miR-378g	CLIP-seq
MIRT2299411	hsa-miR-3916	CLIP-seq
MIRT2299412	hsa-miR-3918	CLIP-seq
MIRT2299413	hsa-miR-3925-5p	CLIP-seq
MIRT2299414	hsa-miR-423-5p	CLIP-seq
MIRT2299415	hsa-miR-4257	CLIP-seq
MIRT2299416	hsa-miR-4271	CLIP-seq
MIRT2299417	hsa-miR-4292	CLIP-seq
MIRT2299418	hsa-miR-4306	CLIP-seq
MIRT2299419	hsa-miR-4330	CLIP-seq
MIRT2299420	hsa-miR-4435	CLIP-seq
MIRT2299421	hsa-miR-4436b-3p	CLIP-seq
MIRT2299422	hsa-miR-4446-3p	CLIP-seq
MIRT2299423	hsa-miR-4458	CLIP-seq
MIRT2299424	hsa-miR-4459	CLIP-seq
MIRT2299425	hsa-miR-4484	CLIP-seq
MIRT2299426	hsa-miR-4488	CLIP-seq
MIRT2299427	hsa-miR-4491	CLIP-seq
MIRT2299428	hsa-miR-4492	CLIP-seq
MIRT2299429	hsa-miR-4498	CLIP-seq
MIRT2299430	hsa-miR-4500	CLIP-seq
MIRT2299431	hsa-miR-4505	CLIP-seq
MIRT2299432	hsa-miR-4515	CLIP-seq
MIRT2299433	hsa-miR-4530	CLIP-seq
MIRT2299434	hsa-miR-4534	CLIP-seq
MIRT2299435	hsa-miR-4640-5p	CLIP-seq
MIRT2299436	hsa-miR-4644	CLIP-seq
MIRT2299437	hsa-miR-4645-5p	CLIP-seq
MIRT2299438	hsa-miR-4656	CLIP-seq
MIRT2299439	hsa-miR-4657	CLIP-seq
MIRT2299440	hsa-miR-4667-5p	CLIP-seq
MIRT2299441	hsa-miR-4668-5p	CLIP-seq
MIRT2299442	hsa-miR-4673	CLIP-seq
MIRT2299443	hsa-miR-4675	CLIP-seq
MIRT2299444	hsa-miR-4685-5p	CLIP-seq
MIRT2299445	hsa-miR-4688	CLIP-seq
MIRT2299446	hsa-miR-4697-5p	CLIP-seq
MIRT2299447	hsa-miR-4699-3p	CLIP-seq
MIRT2299448	hsa-miR-4700-5p	CLIP-seq
MIRT2299449	hsa-miR-4722-5p	CLIP-seq
MIRT2299450	hsa-miR-4725-3p	CLIP-seq
MIRT2299451	hsa-miR-4726-5p	CLIP-seq
MIRT2299452	hsa-miR-4731-5p	CLIP-seq
MIRT2299453	hsa-miR-4740-5p	CLIP-seq
MIRT2299454	hsa-miR-4741	CLIP-seq
MIRT2299455	hsa-miR-4755-3p	CLIP-seq
MIRT2299456	hsa-miR-4764-5p	CLIP-seq
MIRT2299457	hsa-miR-4776-5p	CLIP-seq
MIRT2299458	hsa-miR-4779	CLIP-seq
MIRT2299459	hsa-miR-4788	CLIP-seq
MIRT2299460	hsa-miR-486-3p	CLIP-seq
MIRT2299461	hsa-miR-548an	CLIP-seq
MIRT2299462	hsa-miR-612	CLIP-seq
MIRT2299463	hsa-miR-634	CLIP-seq
MIRT2299464	hsa-miR-658	CLIP-seq
MIRT2299465	hsa-miR-761	CLIP-seq
MIRT2299466	hsa-miR-762	CLIP-seq
MIRT2299467	hsa-miR-767-5p	CLIP-seq
MIRT2299468	hsa-miR-98	CLIP-seq
MIRT2299398	hsa-miR-3125	CLIP-seq
MIRT2299411	hsa-miR-3916	CLIP-seq

Show/Hide all(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
GO:0000776	Component	Kinetochore	IDA	15371340
GO:0000776	Component	Kinetochore	IEA
GO:0000776	Component	Kinetochore	NAS	21633384, 23418356
GO:0000922	Component	Spindle pole	NAS	21633384
GO:0000940	Component	Outer kinetochore	IDA	24530301
GO:0003713	Function	Transcription coactivator activity	IMP	11256947
GO:0003713	Function	Transcription coactivator activity	TAS	10419538
GO:0005515	Function	Protein binding	IPI	15371340, 15502821, 20360068, 24981860, 25416956, 26496610, 28514442, 32296183, 32814053, 32911434, 35271311, 37398436
GO:0005634	Component	Nucleus	IEA
GO:0005634	Component	Nucleus	NAS	21633384
GO:0005654	Component	Nucleoplasm	IDA
GO:0005667	Component	Transcription regulator complex	TAS	10419538
GO:0005694	Component	Chromosome	IEA
GO:0005794	Component	Golgi apparatus	IDA
GO:0005829	Component	Cytosol	TAS
GO:0006366	Process	Transcription by RNA polymerase II	TAS	10419538
GO:0007059	Process	Chromosome segregation	IBA
GO:0007059	Process	Chromosome segregation	IEA
GO:0007059	Process	Chromosome segregation	IMP	15502821
GO:0008608	Process	Attachment of spindle microtubules to kinetochore	NAS	21633384
GO:0043522	Function	Leucine zipper domain binding	IPI	11256947
GO:0045893	Process	Positive regulation of DNA-templated transcription	IEA
GO:0051301	Process	Cell division	IEA

MIM	HGNC	e!Ensembl
609176	9112	ENSG00000160783

	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

Show/Hide Unknown Diseases (2)

Disease merge term	Disease name	Evidence	References	Source
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Ischemic Stroke	Ischemic stroke	N/A	N/A	GWAS
Parkinson disease	Parkinson disease	N/A	N/A	GWAS

Show/Hide Text Mining Associations (4)

Disease Name	Relationship Type	References
Associations from Text Mining Disease associations identified through Pubtator
Cerebral Hemorrhage	Associate	37787451
Cerebral Small Vessel Diseases	Associate	31430377
COVID 19	Associate	37794074
Stroke	Associate	36958462

PMF1 (polyamine modulated factor 1)