TENM4, teneurin transmembrane protein 4, 26011

N. diseases: 44; N. variants: 52
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs865922915
rs865922915
Entrez Id: 26011
Gene Symbol: TENM4
TENM4
CUI: C0036341
Disease:
Schizophrenia
0.010 GeneticVariation BEFREE We herein performed exome sequencing in a Han Chinese schizophrenia family and identified a missense mutation (c.6724C>T, p.R2242C) in the teneurin transmembrane protein 4 (<i>TENM4</i>) gene in the SCZD2 locus, a region previously linked to schizophrenia at 11q14-21. 30745909 2018
dbSNP: rs754333774
rs754333774
Entrez Id: 26011;100126333
Gene Symbol: TENM4;MIR708
TENM4;MIR708
CUI: C0005586
Disease:
Bipolar Disorder
0.010 GeneticVariation BEFREE Three variants detected by HRM were selected to be genotyped. rs754333774 was detected in three cases of BD, two cases of schizophrenia, and no controls. 27864917 2016
dbSNP: rs11237828
rs11237828
Entrez Id: 26011;100847000
Gene Symbol: TENM4;MIR5579
TENM4;MIR5579
CUI: C2931822
Disease:
Nasopharyngeal carcinoma
0.010 GeneticVariation BEFREE In this study, we analyzed associations between eight SNPs in miRNA mature sequences (i.e., rs3746444T>C in hsa-mir-499, rs4919510C>G in hsa-mir-608, rs13299349G>A in hsa-mir-3152, rs12220909G>C in hsa-mir-4293, rs2168518G>A in hsa-mir-4513, rs8078913T>C in hsa-mir-4520a, rs11237828T>C in hsa-mir-5579, and rs9295535T>C in hsa-mir-5689) and NPC susceptibility in southern China with 906 NPC cases and 1072 cancer-free controls, and validated the significant findings in eastern China with 684 cases and 907 healthy controls. 25861865 2015
dbSNP: rs12290811
rs12290811
Entrez Id: 26011
Gene Symbol: TENM4
TENM4
CUI: C0006287
Disease:
Bronchopulmonary Dysplasia
0.010 GeneticVariation BEFREE One SNP, rs12290811, located in the ODZ4 gene reached statistical significance (p=1.7×10(-4), Allelic odds ratio=1.21), a value very near to those reported in previous GWAS of BPD patients. 25124521 2014
dbSNP: rs12290811
rs12290811
Entrez Id: 26011
Gene Symbol: TENM4
TENM4
CUI: C0006012
Disease:
Borderline Personality Disorder
0.010 GeneticVariation BEFREE One SNP, rs12290811, located in the ODZ4 gene reached statistical significance (p=1.7×10(-4), Allelic odds ratio=1.21), a value very near to those reported in previous GWAS of BPD patients. 25124521 2014
dbSNP: rs10751301
rs10751301
Entrez Id: 26011
Gene Symbol: TENM4
TENM4
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.010 GeneticVariation BEFREE Recently, rs10906115 in CDC123/CAMK1D, rs1359790 near SPRY2, rs1436955 in C2CD4A/C2CD4B and rs10751301 in ODZ4 were identified as genetic risk variants for type 2 diabetes by a genome-wide association study in a Chinese population. 21909839 2011
dbSNP: rs12275127
rs12275127
Entrez Id: 26011
Gene Symbol: TENM4
TENM4
CUI: C0596887
Disease:
mathematical ability
A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs10501434
rs10501434
Entrez Id: 26011
Gene Symbol: TENM4
TENM4
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs10793371
rs10793371
Entrez Id: 26011
Gene Symbol: TENM4
TENM4
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs12576775
rs12576775
Entrez Id: 26011
Gene Symbol: TENM4
TENM4
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs12576775
rs12576775
Entrez Id: 26011
Gene Symbol: TENM4
TENM4
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs12788335
rs12788335
Entrez Id: 26011
Gene Symbol: TENM4
TENM4
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs17138230
rs17138230
Entrez Id: 26011
Gene Symbol: TENM4
TENM4
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs1938946
rs1938946
Entrez Id: 26011
Gene Symbol: TENM4
TENM4
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs2187172
rs2187172
Entrez Id: 26011
Gene Symbol: TENM4
TENM4
CUI: C0684249
Disease:
Carcinoma of lung
A 0.700 GeneticVariation GWASCAT Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes. 28604730 2017
dbSNP: rs471435
rs471435
Entrez Id: 26011
Gene Symbol: TENM4
TENM4
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs533870
rs533870
Entrez Id: 26011
Gene Symbol: TENM4
TENM4
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs533870
rs533870
Entrez Id: 26011
Gene Symbol: TENM4
TENM4
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs536962
rs536962
Entrez Id: 26011
Gene Symbol: TENM4
TENM4
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs550547
rs550547
Entrez Id: 26011
Gene Symbol: TENM4
TENM4
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs556857
rs556857
Entrez Id: 26011
Gene Symbol: TENM4
TENM4
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs575257
rs575257
Entrez Id: 26011
Gene Symbol: TENM4
TENM4
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs7932890
rs7932890
Entrez Id: 26011
Gene Symbol: TENM4
TENM4
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs7947534
rs7947534
Entrez Id: 26011
Gene Symbol: TENM4
TENM4
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs201191369
rs201191369
Entrez Id: 26011
Gene Symbol: TENM4
TENM4
CUI: C4225223
Disease:
TREMOR, HEREDITARY ESSENTIAL, 5
0.700 GeneticVariation UNIPROT Missense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremor. 26188006 2015