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Gene id 201254
Gene Summary    Protein Summary    Gene ontology    KEGG pathways    Diseases    PubMed    

Gene Summary

Gene Symbol CENPX   Gene   UCSC   Ensembl
Aliases CENP-X, D9, FAAP10, MHF2, STRA13
Gene name centromere protein X
Alternate names centromere protein X, FANCM associated histone fold protein 2, FANCM-interacting histone fold protein 2, Fanconi anemia-associated polypeptide of 10 kDa, retinoic acid-inducible gene D9 protein homolog, stimulated by retinoic acid 13 homolog, stimulated by reti,
Gene location 17q25.3 (82022929: 82018702)     Exons: 4     NC_000017.11
OMIM 615128

Protein Summary

Protein general information A8MT69  

Name: Centromere protein X (CENP X) (FANCM associated histone fold protein 2) (FANCM interacting histone fold protein 2) (Fanconi anemia associated polypeptide of 10 kDa) (Retinoic acid inducible gene D9 protein homolog) (Stimulated by retinoic acid gene 13 pro

Length: 81  Mass: 8959

Sequence MEGAGAGSGFRKELVSRLLHLHFKDDKTKVSGDALQLMVELLKVFVVEAAVRGVRQAQAEDALRVDVDQLEKVLP
QLLLDF
Structural information
Interpro:  IPR018552  

PDB:  
4DRA 4DRB 4E44 4E45 4NDY 4NE1 4NE3 4NE5 4NE6
PDBsum:   4DRA 4DRB 4E44 4E45 4NDY 4NE1 4NE3 4NE5 4NE6
MINT:  
STRING:   ENSP00000376168
Other Databases GeneCards:  CENPX  Malacards:  CENPX

Gene ontology

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GO accessionTerm nameEvidence codeGo category
GO:0000712 resolution of meiotic rec
ombination intermediates
IBA biological process
GO:0043240 Fanconi anaemia nuclear c
omplex
IBA cellular component
GO:0031297 replication fork processi
ng
IBA biological process
GO:0071821 FANCM-MHF complex
IBA cellular component
GO:0071821 FANCM-MHF complex
IDA cellular component
GO:0003690 double-stranded DNA bindi
ng
IDA contributes to
GO:0043240 Fanconi anaemia nuclear c
omplex
IDA cellular component
GO:0043240 Fanconi anaemia nuclear c
omplex
IDA cellular component
GO:0003677 DNA binding
IDA molecular function
GO:0031297 replication fork processi
ng
IMP biological process
GO:0031398 positive regulation of pr
otein ubiquitination
TAS biological process
GO:0005515 protein binding
IPI molecular function
GO:0000712 resolution of meiotic rec
ombination intermediates
IMP biological process
GO:0006281 DNA repair
IEA biological process
GO:0051382 kinetochore assembly
IEA biological process
GO:0051301 cell division
IEA biological process
GO:0000776 kinetochore
IEA cellular component
GO:0006281 DNA repair
IEA biological process
GO:0007049 cell cycle
IEA biological process
GO:0000775 chromosome, centromeric r
egion
IEA cellular component
GO:0003677 DNA binding
IEA molecular function
GO:0005694 chromosome
IEA cellular component
GO:0005634 nucleus
IEA cellular component
GO:0006974 cellular response to DNA
damage stimulus
IEA biological process
GO:0005654 nucleoplasm
TAS cellular component
GO:0005654 nucleoplasm
TAS cellular component
GO:0005654 nucleoplasm
TAS cellular component
GO:0005654 nucleoplasm
TAS cellular component
GO:0005654 nucleoplasm
TAS cellular component
GO:0005654 nucleoplasm
TAS cellular component
GO:0005654 nucleoplasm
TAS cellular component
GO:0005654 nucleoplasm
TAS cellular component
GO:0005654 nucleoplasm
TAS cellular component
GO:0005654 nucleoplasm
TAS cellular component
GO:0005654 nucleoplasm
TAS cellular component
GO:0005654 nucleoplasm
TAS cellular component
GO:0005654 nucleoplasm
TAS cellular component
GO:0005654 nucleoplasm
TAS cellular component
GO:0034080 CENP-A containing nucleos
ome assembly
TAS biological process
GO:0036297 interstrand cross-link re
pair
TAS biological process
GO:0005515 protein binding
IPI molecular function
GO:0005515 protein binding
IPI molecular function
GO:0005515 protein binding
IPI molecular function
GO:0005515 protein binding
IPI molecular function
GO:0000775 chromosome, centromeric r
egion
IEA cellular component
GO:0005634 nucleus
IEA cellular component
GO:0000777 condensed chromosome kine
tochore
IEA cellular component

KEGG pathways

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Pathway idPathway name
hsa03460Fanconi anemia pathway
Associated diseases References
Aberrant CpGs in Low Motility Sperm MIK: 21674046
Teratozoospermia MIK: 17327269

PubMed references

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PMID Condition Mutation Ethnicity Population details Infertility_type Associated_genes Abstract
17327269 Teratozoos
permia

19 (6 controls
, 13 cases)
Male infertility GSE6872 analyzed by GEO2R (cutoff 1.5 fold)
Show abstract
21674046 Aberrant C
pGs in Low
Motility
Sperm

18
Male infertility GSE26881
Show abstract