FAM47E (family with sequence similarity 47 member E)

Gene

• Entrez ID: 100129583
• Gene name: Family with sequence similarity 47 member E
• Gene symbol: FAM47E
• Synonyms (NCBI Gene): -
• Chromosome: 4
• Chromosome location: 4q21.1

miRNA

miRTarBase ID	miRNA	Experiments	Reference
MIRT044116	hsa-miR-30e-3p	CLASH	23622248
MIRT985457	hsa-miR-1262	CLIP-seq
MIRT985458	hsa-miR-142-5p	CLIP-seq
MIRT985459	hsa-miR-300	CLIP-seq
MIRT985460	hsa-miR-381	CLIP-seq
MIRT985461	hsa-miR-4666-3p	CLIP-seq
MIRT985462	hsa-miR-4698	CLIP-seq
MIRT985463	hsa-miR-4701-3p	CLIP-seq
MIRT985464	hsa-miR-548a-5p	CLIP-seq
MIRT985465	hsa-miR-548ab	CLIP-seq
MIRT985466	hsa-miR-548ak	CLIP-seq
MIRT985467	hsa-miR-548b-5p	CLIP-seq
MIRT985468	hsa-miR-548c-5p	CLIP-seq
MIRT985469	hsa-miR-548d-5p	CLIP-seq
MIRT985470	hsa-miR-548h	CLIP-seq
MIRT985471	hsa-miR-548i	CLIP-seq
MIRT985472	hsa-miR-548j	CLIP-seq
MIRT985473	hsa-miR-548k	CLIP-seq
MIRT985474	hsa-miR-548l	CLIP-seq
MIRT985475	hsa-miR-548w	CLIP-seq
MIRT985476	hsa-miR-548y	CLIP-seq
MIRT985477	hsa-miR-559	CLIP-seq
MIRT2449351	hsa-miR-1277	CLIP-seq
MIRT2449352	hsa-miR-3163	CLIP-seq
MIRT2449353	hsa-miR-4668-3p	CLIP-seq

Gene ontology (GO)

GO ID	Ontology	Definition	Evidence	Reference
GO:0000785	Component	Chromatin	IBA
GO:0000785	Component	Chromatin	IDA	33376131
GO:0005515	Function	Protein binding	IPI	33376131
GO:0005634	Component	Nucleus	IDA	33376131
GO:0005634	Component	Nucleus	IEA
GO:0005694	Component	Chromosome	IEA
GO:0005737	Component	Cytoplasm	IDA	25231882, 33376131
GO:0005737	Component	Cytoplasm	IEA
GO:0006325	Process	Chromatin organization	IEA
GO:0008047	Function	Enzyme activator activity	IMP	33376131
GO:0045815	Process	Transcription initiation-coupled chromatin remodeling	IBA
GO:0045815	Process	Transcription initiation-coupled chromatin remodeling	IMP	33376131
GO:0071168	Process	Protein localization to chromatin	IMP	33376131

Other IDs

• MIM: HGNC
• HGNC: N/A
• e!Ensembl: HGNC

Interactions View interactions

Associated diseases

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