FPGT-TNNI3K (FPGT-TNNI3K readthrough)

Gene Gene information from NCBI Gene database.
Gene miRNA Other IDs Associated diseases
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
Gene miRNA Other IDs Associated diseases
Show/Hide all (5)
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.
Gene miRNA Other IDs Associated diseases
MIM HGNC e!Ensembl
HGNC N/A HGNC
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
2
Gene miRNA Other IDs Associated diseases
Show/Hide Unknown Diseases (2)
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Atrial conduction disease Uncertain significance rs199608014 RCV001198229
FPGT-TNNI3K-related disorder Likely benign rs45606732 RCV003944664