About Us

Search Result


Gene id 90529
Gene Summary    Protein Summary    Gene ontology    Diseases    PubMed    

Gene Summary

Gene Symbol STPG1   Gene   UCSC   Ensembl
Aliases C1orf201, MAPO2
Gene name sperm tail PG-rich repeat containing 1
Alternate names O(6)-methylguanine-induced apoptosis 2, O6-methylguanine-induced apoptosis 2, UPF0490 protein C1orf201, sperm-tail PG-rich repeat-containing protein 1,
Gene location 1p36.11 (24415532: 24356998)     Exons: 12     NC_000001.11
OMIM 607795

Protein Summary

Protein general information Q5TH74  

Name: O(6) methylguanine induced apoptosis 2 (MAPO2) (Sperm tail PG rich repeat containing protein 1)

Length: 334  Mass: 36786

Sequence MDNSAQKNERTGKHPRRASEVQKGFTAAYPTQSSIPFKSQASVIPESEKKGFNSQAKRFPHKKNDIPGPGFYNVI
HQSPVSNSVSLSKKGTCMFPSMCARLDTIISKYPAANAYTIPSDFISKRDFSNSCSSMFQLPSFMKALKFETPAP
NYYNASVSCCKQRNNVCTRAGFMSKTQRGSFAFADKGPPPGHYDINESLVKQSPNTLMSCFKSKTNRGLKLTSTG
PGPGYYNPSDCTKVPKKTLFPKNPILNFSAQPSPLPPKPPFPGPGQYEIVDYLGPRKHFISSASFVSNTSRWTAA
PPQPGLPGPATYKPELPGKQSFLYNEDKKWIPVL
Structural information
Interpro:  IPR010736  
STRING:   ENSP00000363530
Other Databases GeneCards:  STPG1  Malacards:  STPG1

Gene ontology

Expand All | Collapse All

GO accessionTerm nameEvidence codeGo category
GO:1902110 positive regulation of mi
tochondrial membrane perm
eability involved in apop
totic process
IBA biological process
GO:0005737 cytoplasm
IEA cellular component
GO:0006915 apoptotic process
IEA biological process
GO:0005634 nucleus
IEA cellular component
GO:0005737 cytoplasm
IEA cellular component
GO:0005634 nucleus
IEA cellular component
GO:0005739 mitochondrion
IEA cellular component
GO:0005739 mitochondrion
IEA cellular component
GO:0043065 positive regulation of ap
optotic process
IMP biological process
GO:0003674 molecular_function
ND molecular function
GO:1902110 positive regulation of mi
tochondrial membrane perm
eability involved in apop
totic process
IMP biological process
Associated diseases References
Spermatogenic defects MIK: 31037746

PubMed references

Expand All | Collapse All

PMID Condition Mutation Ethnicity Population details Infertility_type Associated_genes Abstract
31037746 Spermatoge
nic defect
s

16 (1 control,
15 cases)
Male infertility GSE6023 analyzed using GEO2R
Show abstract