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:0003674	Function	Molecular_function	ND
GO:0005737	Component	Cytoplasm	IDA	25231882
GO:0008150	Process	Biological_process	ND

Other IDs

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

Associated diseases

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, rs119451946, rs80356771, rs74500255, rs75822236, rs1141814, rs78973108, rs121908681, rs121908686, rs121908687, rs137853054, rs137853055, rs137853056, rs137853057, rs137853058, rs137853059, rs34424986, rs137853060, rs397518439, rs28938172, rs74315351, rs74315353, rs137853051, rs118192098, rs121918104, rs1589451049, rs104893877, rs104893878, rs188286943, rs387906863, rs387906864, rs774631197, rs199935023, rs397514694, rs398122403, rs398122404, rs398122405, rs104886460, rs409652, rs431905511, rs63751392, rs756677845, rs864309527, rs864309650, rs750014782, rs1554391082, rs864622011, rs869312810, rs869312809, rs869312811, rs369100678, rs879253853, rs869320761, rs747506979, rs879255630, rs886039854, rs191486604, rs781442277, rs1060499619, rs751037529, rs55777503, rs768091663, rs34208370, rs1553122929, rs772786691, rs754809877, rs1555907463, rs1557561340, rs781600849, rs141263564, rs1557901552, rs777160388, rs756783990, rs867929413, rs1237637353, rs1005937012, rs755000580, rs747427602, rs1578089802, rs771586218, rs748142049, rs1582953433, rs746646126, rs771529549, rs121918106	21738487, 27182965, 28892059, 19915575, 25064009

Unknown
Disease term	Disease name	Evidence	References	Source
Parkinson Disease	Parkinson Disease			GWAS

Associations from Text Mining
Disease Name	Relationship Type	References
Autism Spectrum Disorder	Associate	38421723
Chronic Kidney Disease Mineral and Bone Disorder	Associate	25231882
Developmental Disabilities	Associate	38421723
Enterovirus Infections	Associate	34193186
Hand Foot and Mouth Disease	Associate	34193186
Parkinson Disease	Associate	21738487, 23419877, 30957308