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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
2 associated genes
No signs/symptoms info
Male infertility associated with large-headed multiflagellar polyploid spermatozoa
Hereditary site-specific ovarian cancer syndrome

AURKC BRCA1
BRCA2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
AURKC
(0.63)
BRCA1



Citations in the biomedical literature:


Male infertility associated with large-headed multiflagellar polyploid spermatozoa
AURKC
Hereditary site-specific ovarian cancer syndrome
BRCA1 BRCA2



Male infertility associated with large-headed multiflagellar polyploid spermatozoa
Hereditary site-specific ovarian cancer syndrome

Classification (Orphanet):
- Rare genetic disease
- Rare infertility
Classification (Orphanet):
- Rare genetic disease
- Rare gynecologic or obstetric disease
- Rare oncologic disease

Classification (ICD10):
- Diseases of the genitourinary system -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.