FAM47E-STBD1 (FAM47E-STBD1 readthrough)

Gene
Gene miRNA Other IDs Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
100631383
Gene name Gene Name - the full gene name approved by the HGNC.
FAM47E-STBD1 readthrough
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
FAM47E-STBD1
Synonyms (NCBI Gene) Gene synonyms aliases
FAM47E
Chromosome Chromosome number
4
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
4q21.1
Summary Summary of gene provided in NCBI Entrez Gene.
This locus represents naturally occurring read-through transcription between the neighboring FAM47E (family with sequence similarity 47, member E) and STBD1 (starch binding domain 1) genes on chromosome 4. The read-through transcript encodes a protein tha
miRNA miRNA information provided by mirtarbase database.
Gene miRNA Other IDs Associated diseases
Show/Hide all(24)
miRTarBase ID miRNA Experiments Reference
MIRT707666 hsa-miR-8485 HITS-CLIP 21572407
MIRT707665 hsa-miR-329-3p HITS-CLIP 21572407
MIRT707664 hsa-miR-362-3p HITS-CLIP 21572407
MIRT707663 hsa-miR-603 HITS-CLIP 21572407
MIRT707662 hsa-miR-4789-3p HITS-CLIP 21572407
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene miRNA Other IDs Associated diseases
MIM HGNC e!Ensembl
HGNC N/A HGNC
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Gene miRNA Other IDs Associated diseases
Show/Hide Causal Diseases (1)
Causal
Disease term Disease name dbSNP ID References
Parkinson disease Parkinson Disease rs33939927, rs35801418, rs34805604, rs35870237, rs34995376, rs74315355, rs28940284, rs74315356, rs74315357, rs28940285, rs730880302, rs750664040, rs74315359, rs74315360, rs45539432
View all (84 more)		 28892059, 27182965, 19915575, 21738487, 25064009