Entity Details

Primary name PMFBP1
Entity type gene
Source Source Link

Details

PrimaryID83449
RefseqGene
SymbolPMFBP1
Namepolyamine modulated factor 1 binding protein 1
Chromosome16
Location16q22.2
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2001-05-27
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsPMFBP_HUMAN

GO terms

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GOName
GO:0005737 cytoplasm
GO:0007283 spermatogenesis
GO:0097224 sperm connecting piece

Diseases

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Disease IDSourceNameDescription
618112 OMIMSpermatogenic failure 31 (SPGF31)An autosomal recessive infertility disorder caused by spermatogenesis defects that result in oligozoospermia with a high proportion of acephalic sperm. The disease is caused by variants affecting the gene represented in this entry.

Interactions

6 interactions

InteractorPartnerSourcesPublicationsLink
PMFBP1MKLN1BioGRID, IntAct27173435 unassigned1312 details
PMFBP1AAMPBioGRID, IntAct27173435 unassigned1312 details
PMFBP1MMADHCBioGRID, IntAct27173435 unassigned1312 details
PMFBP1SLC25A5BioGRID, IntAct30021884 details
PMFBP1RPL15BioGRID, IntAct30021884 details
PMFBP1CHMP4BBioGRID31586073 details