Colorectal Carcinoma
|
0.310 |
GeneticVariation
|
disease |
UNIPROT |
|
|
|
hearing impairment
|
0.110 |
Biomarker
|
phenotype |
HPO |
|
|
|
Sensorineural Hearing Loss (disorder)
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
|
|
|
Breast Carcinoma
|
0.110 |
GeneticVariation
|
disease |
GWASCAT |
Association analysis identifies 65 new breast cancer risk loci.
|
29059683 |
2017 |
Deafness
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
Auditory hair cells of postnatal Cdc14a mutants develop normally, but subsequently degenerate causing deafness.
|
29293958 |
2018 |
DEAFNESS, AUTOSOMAL RECESSIVE 32
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
CDC14A phosphatase is essential for hearing and male fertility in mouse and human.
|
29293958 |
2018 |
DEAFNESS, AUTOSOMAL RECESSIVE 32
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
CDC14A phosphatase is essential for hearing and male fertility in mouse and human.
|
29293958 |
2018 |
DEAFNESS, AUTOSOMAL RECESSIVE 32
|
0.700 |
Biomarker
|
disease |
CTD_human |
CDC14A phosphatase is essential for hearing and male fertility in mouse and human.
|
29293958 |
2018 |
DEAFNESS, AUTOSOMAL RECESSIVE 32
|
0.700 |
GeneticVariation
|
disease |
CLINVAR |
CDC14A phosphatase is essential for hearing and male fertility in mouse and human.
|
29293958 |
2018 |
Nonsyndromic Deafness
|
0.320 |
Biomarker
|
disease |
CLINGEN |
CDC14A phosphatase is essential for hearing and male fertility in mouse and human.
|
29293958 |
2018 |
Prelingual Deafness
|
0.300 |
Biomarker
|
disease |
CTD_human |
CDC14A phosphatase is essential for hearing and male fertility in mouse and human.
|
29293958 |
2018 |
Male infertility
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
CDC14A phosphatase is essential for hearing and male fertility in mouse and human.
|
29293958 |
2018 |
Oligospermia
|
0.300 |
Biomarker
|
disease |
CTD_human |
CDC14A phosphatase is essential for hearing and male fertility in mouse and human.
|
29293958 |
2018 |
Hearing Loss, Extreme
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
CDC14A phosphatase is essential for hearing and male fertility in mouse and human.
|
29293958 |
2018 |
Complete Hearing Loss
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
CDC14A phosphatase is essential for hearing and male fertility in mouse and human.
|
29293958 |
2018 |
Deafness, Acquired
|
0.300 |
Biomarker
|
disease |
CTD_human |
CDC14A phosphatase is essential for hearing and male fertility in mouse and human.
|
29293958 |
2018 |
Subfertility, Male
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
CDC14A phosphatase is essential for hearing and male fertility in mouse and human.
|
29293958 |
2018 |
Male sterility
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
CDC14A phosphatase is essential for hearing and male fertility in mouse and human.
|
29293958 |
2018 |
Bilateral Deafness
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
CDC14A phosphatase is essential for hearing and male fertility in mouse and human.
|
29293958 |
2018 |
Deaf Mutism
|
0.300 |
Biomarker
|
disease |
CTD_human |
CDC14A phosphatase is essential for hearing and male fertility in mouse and human.
|
29293958 |
2018 |
Breast Carcinoma
|
0.110 |
Biomarker
|
disease |
BEFREE |
In gene-level analyses, CDC25C, SCC1/RAD21, TLK2, and SMC6L1 were associated (P < 0.05) with overall breast cancer risk, CDC6, CDC27, SUMO3, RASSF1, KIF2, and CDC14A were associated with high grade breast cancer risk, and EIF3S10 and CDC25A were associated with both.
|
21607584 |
2011 |
Malignant neoplasm of breast
|
0.010 |
Biomarker
|
disease |
BEFREE |
In gene-level analyses, CDC25C, SCC1/RAD21, TLK2, and SMC6L1 were associated (P < 0.05) with overall breast cancer risk, CDC6, CDC27, SUMO3, RASSF1, KIF2, and CDC14A were associated with high grade breast cancer risk, and EIF3S10 and CDC25A were associated with both.
|
21607584 |
2011 |
Body Height
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
|
30595370 |
2019 |
Nodular Sclerosis Classical Hodgkin Lymphoma
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Linkage analysis indicates that in this family the NSHL locus, (DFNB35) maps to a 17.54 cM region on chromosome 14 flanked by markers D14S57 and D14S59.
|
12529709 |
2003 |
Nonsyndromic Deafness
|
0.320 |
GeneticVariation
|
disease |
BEFREE |
Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1.
|
12634867 |
2003 |