Colorectal Carcinoma
|
0.310 |
GeneticVariation
|
disease |
UNIPROT |
|
|
|
hearing impairment
|
0.110 |
Biomarker
|
phenotype |
HPO |
|
|
|
Sensorineural Hearing Loss (disorder)
|
0.100 |
CausalMutation
|
disease |
CLINVAR |
|
|
|
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 |
Malignant Neoplasms
|
0.020 |
GeneticVariation
|
group |
BEFREE |
We also identified a molecular signature for the presence of immunoglobulin variable heavy chain somatic mutation, which includes a number of genes potentially relevant in cancer (CDC14A, ras, and others).
|
14678979 |
2003 |
Primary malignant neoplasm
|
0.020 |
GeneticVariation
|
group |
BEFREE |
We also identified a molecular signature for the presence of immunoglobulin variable heavy chain somatic mutation, which includes a number of genes potentially relevant in cancer (CDC14A, ras, and others).
|
14678979 |
2003 |
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 |
Mutations of ESRRB encoding estrogen-related receptor beta cause autosomal-recessive nonsyndromic hearing impairment DFNB35.
|
18179891 |
2008 |
Colorectal Carcinoma
|
0.310 |
GeneticVariation
|
disease |
BEFREE |
The CDC14A and MTMR3 mutations detected in the GC and CRC were deletion or duplication mutations of one base in the nucleotide repeats that would result in premature stops of the amino acid syntheses.
|
20477815 |
2010 |
Malignant Neoplasms
|
0.020 |
GeneticVariation
|
group |
BEFREE |
We found CDC14A and MTMR3 mutations in five and one cancer (s), respectively.
|
20477815 |
2010 |
Primary malignant neoplasm
|
0.020 |
GeneticVariation
|
group |
BEFREE |
We found CDC14A and MTMR3 mutations in five and one cancer (s), respectively.
|
20477815 |
2010 |
Malignant neoplasm of stomach
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
The CDC14A and MTMR3 mutations detected in the GC and CRC were deletion or duplication mutations of one base in the nucleotide repeats that would result in premature stops of the amino acid syntheses.
|
20477815 |
2010 |
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 |
hearing impairment
|
0.110 |
GeneticVariation
|
phenotype |
BEFREE |
Two families with recessive ESRRB mutations and DFNB35 hearing impairment showed more extensive dental destruction by caries.
|
25023176 |
2014 |
Dental caries
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Two families with recessive ESRRB mutations and DFNB35 hearing impairment showed more extensive dental destruction by caries.
|
25023176 |
2014 |
Caries (morphologic abnormality)
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Two families with recessive ESRRB mutations and DFNB35 hearing impairment showed more extensive dental destruction by caries.
|
25023176 |
2014 |
DEAFNESS, AUTOSOMAL RECESSIVE 32
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Mutations in CDC14A, Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound Deafness.
|
27259055 |
2016 |
DEAFNESS, AUTOSOMAL RECESSIVE 32
|
0.700 |
Biomarker
|
disease |
CTD_human |
Mutations in CDC14A, Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound Deafness.
|
27259055 |
2016 |
DEAFNESS, AUTOSOMAL RECESSIVE 32
|
0.700 |
CausalMutation
|
disease |
CLINVAR |
Mutations in CDC14A, Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound Deafness.
|
27259055 |
2016 |
DEAFNESS, AUTOSOMAL RECESSIVE 32
|
0.700 |
GeneticVariation
|
disease |
UNIPROT |
Mutations in CDC14A, Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound Deafness.
|
27259055 |
2016 |
Breast Carcinoma
|
0.110 |
GeneticVariation
|
disease |
GWASCAT |
Association analysis identifies 65 new breast cancer risk loci.
|
29059683 |
2017 |
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 |