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Gene id 171484
Gene Summary    Protein Summary    Gene ontology    Diseases    PubMed    

Gene Summary

Gene Symbol FAM9C   Gene   UCSC   Ensembl
Aliases TEX39C
Gene name family with sequence similarity 9 member C
Alternate names protein FAM9C, testis expressed 39C,
Gene location Xp22.2 (13044792: 13035616)     Exons: 9     NC_000023.11
Gene summary(Entrez) This gene is a member of a gene family which arose through duplication on the X chromosome. The encoded protein may be localized to the nucleus as the protein contains several nuclear localization signals, and has similarity to a synaptonemal complex prot
OMIM 603503

Protein Summary

Protein general information Q8IZT9  

Name: Protein FAM9C

Length: 166  Mass: 19210

Tissue specificity: Expressed exclusively in testis. {ECO

Sequence MAAKDQLEVQVMAAQEMELAGKDPVSHEHEERKPVTETKEGDVTDEHGERGSFAETDEHTGVDTKELEDIAADIK
EHLAAKRKRIEKIAKACSEIKNRIKNVLRTTQLKRQKRDYRISLKLPNVLEEFITDEQKDEEGDGEKEEQIKIFQ
EQQKRWQQDGKGTERD
Structural information
Interpro:  IPR006888  
STRING:   ENSP00000334430
Other Databases GeneCards:  FAM9C  Malacards:  FAM9C

Gene ontology

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GO accessionTerm nameEvidence codeGo category
GO:0051321 meiotic cell cycle
IBA biological process
GO:0007286 spermatid development
IBA biological process
GO:0007283 spermatogenesis
IBA biological process
GO:0000795 synaptonemal complex
IBA cellular component
GO:0005634 nucleus
IEA cellular component
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: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: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:0005634 nucleus
IEA cellular component
Associated diseases References
Aberrant CpGs in Low Motility Sperm MIK: 21674046
Unexplained infertility MIK: 25753583

PubMed references

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PMID Condition Mutation Ethnicity Population details Infertility_type Associated_genes Abstract
21674046 Aberrant C
pGs in Low
Motility
Sperm

18
Male infertility GSE26881
Show abstract
25753583 Unexplaine
d infertil
ity

46 (17 fertile
men, 29 male pa
tients)
Male infertility Microarray
Show abstract