Entity Details

Primary name SUN5
Entity type gene
Source Source Link

Details

PrimaryID140732
RefseqGeneNG_054760
SymbolSUN5
NameSad1 and UNC84 domain containing 5
Chromosome20
Location20q11.21
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2002-01-05
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsSUN5_HUMAN

GO terms

Show/Hide Table
GOName
GO:0005635 nuclear envelope
GO:0005637 nuclear inner membrane
GO:0005794 Golgi apparatus
GO:0006998 nuclear envelope organization
GO:0007283 spermatogenesis
GO:0007286 spermatid development
GO:0016021 integral component of membrane
GO:0034993 meiotic nuclear membrane microtubule tethering complex
GO:0043495 protein-membrane adaptor activity
GO:0097224 sperm connecting piece

Diseases

Show/Hide Table
Disease IDSourceNameDescription
617187 OMIMSpermatogenic failure 16 (SPGF16)An infertility disorder caused by spermatogenesis defects and characterized by abnormally shaped spermatozoa in the semen of affected individuals. Most spermatozoa are made up of headless tails, while a small proportion has an abnormal head-tail junction. A few spermatozoa are made up of tailless heads. The disease is caused by variants affecting the gene represented in this entry.

Interactions

3 interactions

InteractorPartnerSourcesPublicationsLink
SUN5SPAG4BioGRID, IntAct32296183 details
SUN5APPBioGRID21832049 details
SUN5UBCBioGRID23314748 details