FPGT-TNNI3K (FPGT-TNNI3K readthrough)

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Gene Gene information from NCBI Gene database.
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Entrez ID 100526835
Gene name FPGT-TNNI3K readthrough
Gene symbol FPGT-TNNI3K
Synonyms (NCBI Gene)
CARKTNNI3K
Chromosome 1
Chromosome location 1p31.1
Summary This locus represents naturally occurring read-through transcription from the neighboring fucose-1-phosphate guanylyltransferase (FPGT) and TNNI3 interacting kinase (TNNI3K) genes. Alternative splicing results in multiple transcript variants that are comp
miRNA miRNA information provided by mirtarbase database.
5
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miRTarBase ID miRNA Experiments Reference
MIRT016954 hsa-miR-335-5p Microarray 18185580
MIRT016954 hsa-miR-335-5p Microarray 18185580
MIRT1003952 hsa-miR-186 CLIP-seq
MIRT1003953 hsa-miR-197 CLIP-seq
MIRT1003954 hsa-miR-5096 CLIP-seq
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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MIM HGNC e!Ensembl
HGNC N/A HGNC
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
17
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Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Show/Hide Unknown Diseases (17)
Phenotype Name Clinical Significance Source Reference Evidence Score
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2 — Disgenet —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Atrial conduction disease Uncertain significance ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ATRIAL FIBRILLATION — GWAS catalog 40645996
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ATTENTION DEFICIT HYPERACTIVITY DISORDER — GWAS catalog 34446935
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BRONCHIAL DISEASE — GWAS catalog 39024449
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Show/Hide Text Mining Associations (40)
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Adenocarcinoma of large intestine Colorectal Cancer UNIPROT_DG
★★★★★
★☆☆☆☆
Found in Text Mining only
Arrhythmias Cardiac Cardiac arrhythmias Pubtator 37199186 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Atrial Fibrillation Atrial fibrillation Pubtator 24925317, 37199186 Associate
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Atrial Fibrillation Atrial Fibrillation HPO_DG
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY Cardiac Conduction Disease With Or Without Dilated Cardiomyopathy ORPHANET_DG 24925317
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY Cardiac Conduction Disease With Or Without Dilated Cardiomyopathy UNIPROT_DG 24925317
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY Cardiac Conduction Disease With Or Without Dilated Cardiomyopathy GENOMICS_ENGLAND_DG 29355681
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY Cardiac Conduction Disease With Or Without Dilated Cardiomyopathy CLINVAR_DG
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY Cardiac Conduction Disease With Or Without Dilated Cardiomyopathy CTD_human_DG
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Cardiac Conduction System Disease Cardiac conduction disease Pubtator 24925317 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
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TNNI3K 5 shared diseasesDilated cardiomyopathy, Arrhythmogenic right ventricular cardiomyopathy, Bronchial disease, Cardiac conduction disease, Meniere disease 5 shared evidence sourcesDisgenet (Arrhythmogenic right ventricular cardiomyopathy), GWAS catalog (Bronchial disease), Disgenet (Cardiac conduction disease), Disgenet (Dilated cardiomyopathy), Disgenet (Meniere disease) Related via 5 shared diseases including Dilated cardiomyopathy, Arrhythmogenic right ventricular cardiomyopathy — evidence mostly Disgenet. C2orf49 2 shared diseasesDilated cardiomyopathy, Arrhythmogenic right ventricular cardiomyopathy 2 shared evidence sourcesDisgenet (Arrhythmogenic right ventricular cardiomyopathy), Disgenet (Dilated cardiomyopathy) Related via 2 shared diseases including Dilated cardiomyopathy, Arrhythmogenic right ventricular cardiomyopathy — evidence mostly Disgenet. TJP1 2 shared diseasesDilated cardiomyopathy, Arrhythmogenic right ventricular cardiomyopathy 2 shared evidence sourcesDisgenet (Arrhythmogenic right ventricular cardiomyopathy), Disgenet (Dilated cardiomyopathy) Related via 2 shared diseases including Dilated cardiomyopathy, Arrhythmogenic right ventricular cardiomyopathy — evidence mostly Disgenet. FHL2 2 shared diseasesDilated cardiomyopathy, Arrhythmogenic right ventricular cardiomyopathy 2 shared evidence sourcesDisgenet (Arrhythmogenic right ventricular cardiomyopathy), Disgenet (Dilated cardiomyopathy) Related via 2 shared diseases including Dilated cardiomyopathy, Arrhythmogenic right ventricular cardiomyopathy — evidence mostly Disgenet. MYOM1 2 shared diseasesDilated cardiomyopathy, Arrhythmogenic right ventricular cardiomyopathy 2 shared evidence sourcesDisgenet (Arrhythmogenic right ventricular cardiomyopathy), Disgenet (Dilated cardiomyopathy) Related via 2 shared diseases including Dilated cardiomyopathy, Arrhythmogenic right ventricular cardiomyopathy — evidence mostly Disgenet.
Cardiomyopathy Linked via 3 of 5 related genesC2orf49, FHL2, MYOM1 Left ventricular noncompaction cardiomyopathy Linked via 2 of 5 related genesC2orf49, FHL2 Atrial tachyarrhythmia, infra-hisian cardiac conduction disease Linked via 1 of 5 related genesTNNI3K Alzheimer disease Linked via 1 of 5 related genesTJP1 Autism Linked via 1 of 5 related genesTJP1