Gene Details | GeDiPNet - Complete Gene Info, Disease Associations & Pathways

Gene Gene information from NCBI Gene database. Gene miRNA Other IDs Associated diseases
Entrez ID	100631383
Gene name	FAM47E-STBD1 readthrough
Gene symbol	FAM47E-STBD1
Synonyms (NCBI Gene)	FAM47E
Chromosome	4
Chromosome location	4q21.1
Summary	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

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
MIRT707661	hsa-miR-5011-5p	HITS-CLIP	21572407
MIRT707660	hsa-miR-6867-5p	HITS-CLIP	21572407
MIRT707659	hsa-miR-3941	HITS-CLIP	21572407
MIRT707658	hsa-miR-4789-5p	HITS-CLIP	21572407
MIRT707657	hsa-miR-190a-3p	HITS-CLIP	21572407
MIRT707656	hsa-miR-448	HITS-CLIP	21572407
MIRT707655	hsa-miR-574-5p	HITS-CLIP	21572407
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
MIRT707661	hsa-miR-5011-5p	HITS-CLIP	21572407
MIRT707660	hsa-miR-6867-5p	HITS-CLIP	21572407
MIRT707659	hsa-miR-3941	HITS-CLIP	21572407
MIRT707658	hsa-miR-4789-5p	HITS-CLIP	21572407
MIRT707657	hsa-miR-190a-3p	HITS-CLIP	21572407
MIRT707656	hsa-miR-448	HITS-CLIP	21572407
MIRT707655	hsa-miR-574-5p	HITS-CLIP	21572407

MIM	HGNC	e!Ensembl
HGNC	N/A	HGNC

Interactions View interactions

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)

Show/Hide Unknown Diseases (1)

Phenotype Name	Clinical Significance	Source	Evidence Score
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.
PARKINSON DISEASE	—	GWAS catalog	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations

Show/Hide Text Mining Associations (6)

Disease Name	Disease (Merged)	Source	PMID	Relationship Type	Evidence Score
Associations from Text Mining Disease associations identified through text mining
Autism Spectrum Disorder	Autism	Pubtator	38421723	Associate	★★★★★ ★☆☆☆☆ Found in Text Mining only
Developmental Disabilities	Developmental disability	Pubtator	38421723	Associate	★★★★★ ★☆☆☆☆ Found in Text Mining only
Parkinson Disease	Parkinson disease	GWASDB_DG	19915575, 21738487		★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Parkinson Disease	Parkinson disease	GWASCAT_DG	19915575, 21738487, 25064009, 27182965, 28892059		★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Parkinson Disease	Parkinson disease	Pubtator	21738487, 23419877, 30957308	Associate	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Parkinson Disease	Parkinson disease	BEFREE	26224037		★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations

FAM47E-STBD1 (FAM47E-STBD1 readthrough)