MXI1, MAX interactor 1, dimerization protein, 4601

N. diseases: 128; N. variants: 11
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137852603
rs137852603
Entrez Id: 4601
Gene Symbol: MXI1
MXI1
CUI: C0376358
Disease:
Malignant neoplasm of prostate
0.800 GeneticVariation UNIPROT A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment. 25394175 2015
dbSNP: rs137852603
rs137852603
Entrez Id: 4601
Gene Symbol: MXI1
MXI1
CUI: C0376358
Disease:
Malignant neoplasm of prostate
0.800 GeneticVariation UNIPROT Recommendations from the EGAPP Working Group: does PCA3 testing for the diagnosis and management of prostate cancer improve patient health outcomes? 24071797 2014
dbSNP: rs137852603
rs137852603
Entrez Id: 4601
Gene Symbol: MXI1
MXI1
CUI: C0376358
Disease:
Malignant neoplasm of prostate
0.800 GeneticVariation UNIPROT Early detection of prostate cancer: AUA Guideline. 23659877 2013
dbSNP: rs137852603
rs137852603
Entrez Id: 4601
Gene Symbol: MXI1
MXI1
CUI: C0376358
Disease:
Malignant neoplasm of prostate
0.800 GeneticVariation UNIPROT NCCN Task Force report: Evaluating the clinical utility of tumor markers in oncology. 22138009 2011
dbSNP: rs137852603
rs137852603
Entrez Id: 4601
Gene Symbol: MXI1
MXI1
CUI: C0376358
Disease:
Malignant neoplasm of prostate
0.800 GeneticVariation UNIPROT National Academy of Clinical Biochemistry laboratory medicine practice guidelines for use of tumor markers in testicular, prostate, colorectal, breast, and ovarian cancers. 19042984 2008
dbSNP: rs137852603
rs137852603
Entrez Id: 4601
Gene Symbol: MXI1
MXI1
CUI: C0376358
Disease:
Malignant neoplasm of prostate
C 0.800 CausalMutation CLINVAR
dbSNP: rs137852604
rs137852604
Entrez Id: 4601
Gene Symbol: MXI1
MXI1
CUI: C0206729
Disease:
Neurofibrosarcoma
0.710 GeneticVariation BEFREE We discovered a missense mutation, GCA to GTA (Ala 54 Val), in exon 2 in a neurofibrosarcoma patient (case 1), two missense mutations, AAA to CAA (Lys 118 Gln) and GAA to GGA (Glu 154 Gly) in exon 5 of another neurofibrosarcoma patient (case 2), and 3 amino acid substitutions, GTG to GCG (Val 179 Ala), GTT to GCT (Val 181 Ala) and TTC to CTC (Phe 186 Leu), in a third neurofibrosarcoma patient (case 3). 10470286 1999
dbSNP: rs137852604
rs137852604
Entrez Id: 4601
Gene Symbol: MXI1
MXI1
CUI: C0206729
Disease:
Neurofibrosarcoma
T 0.710 CausalMutation CLINVAR
dbSNP: rs11195062
rs11195062
Entrez Id: 4601
Gene Symbol: MXI1
MXI1
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs113511609
rs113511609
Entrez Id: 4601
Gene Symbol: MXI1
MXI1
CUI: C0023508
Disease:
White Blood Cell Count procedure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1475502
rs1475502
Entrez Id: 4601
Gene Symbol: MXI1
MXI1
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1967840
rs1967840
Entrez Id: 4601
Gene Symbol: MXI1
MXI1
CUI: C0005612
Disease:
Birth Weight
A 0.700 GeneticVariation GWASCAT Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. 31043758 2019
dbSNP: rs2855469
rs2855469
Entrez Id: 4601
Gene Symbol: MXI1
MXI1
CUI: C0007222
Disease:
Cardiovascular Diseases
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs111777102
rs111777102
Entrez Id: 4601
Gene Symbol: MXI1
MXI1
CUI: C0428883
Disease:
Diastolic blood pressure
C 0.700 GeneticVariation GWASCAT Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. 30224653 2018
dbSNP: rs17127170
rs17127170
Entrez Id: 4601
Gene Symbol: MXI1
MXI1
CUI: C0032181
Disease:
Platelet Count measurement
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs387906417
rs387906417
Entrez Id: 4601
Gene Symbol: MXI1
MXI1
CUI: C0376358
Disease:
Malignant neoplasm of prostate
C 0.700 CausalMutation CLINVAR
dbSNP: rs137852604
rs137852604
Entrez Id: 4601
Gene Symbol: MXI1
MXI1
CUI: C0751690
Disease:
Malignant Peripheral Nerve Sheath Tumor
0.010 GeneticVariation BEFREE We discovered a missense mutation, GCA to GTA (Ala 54 Val), in exon 2 in a neurofibrosarcoma patient (case 1), two missense mutations, AAA to CAA (Lys 118 Gln) and GAA to GGA (Glu 154 Gly) in exon 5 of another neurofibrosarcoma patient (case 2), and 3 amino acid substitutions, GTG to GCG (Val 179 Ala), GTT to GCT (Val 181 Ala) and TTC to CTC (Phe 186 Leu), in a third neurofibrosarcoma patient (case 3). 10470286 1999
dbSNP: rs759049323
rs759049323
Entrez Id: 4601
Gene Symbol: MXI1
MXI1
CUI: C0751690
Disease:
Malignant Peripheral Nerve Sheath Tumor
0.010 GeneticVariation BEFREE We discovered a missense mutation, GCA to GTA (Ala 54 Val), in exon 2 in a neurofibrosarcoma patient (case 1), two missense mutations, AAA to CAA (Lys 118 Gln) and GAA to GGA (Glu 154 Gly) in exon 5 of another neurofibrosarcoma patient (case 2), and 3 amino acid substitutions, GTG to GCG (Val 179 Ala), GTT to GCT (Val 181 Ala) and TTC to CTC (Phe 186 Leu), in a third neurofibrosarcoma patient (case 3). 10470286 1999
dbSNP: rs759049323
rs759049323
Entrez Id: 4601
Gene Symbol: MXI1
MXI1
CUI: C0206729
Disease:
Neurofibrosarcoma
0.010 GeneticVariation BEFREE We discovered a missense mutation, GCA to GTA (Ala 54 Val), in exon 2 in a neurofibrosarcoma patient (case 1), two missense mutations, AAA to CAA (Lys 118 Gln) and GAA to GGA (Glu 154 Gly) in exon 5 of another neurofibrosarcoma patient (case 2), and 3 amino acid substitutions, GTG to GCG (Val 179 Ala), GTT to GCT (Val 181 Ala) and TTC to CTC (Phe 186 Leu), in a third neurofibrosarcoma patient (case 3). 10470286 1999