FAM184A (family with sequence similarity 184 member A)

Gene

• Entrez ID: 79632
• Gene name: Family with sequence similarity 184 member A
• Gene symbol: FAM184A
• Synonyms (NCBI Gene): C6orf60
• Chromosome: 6
• Chromosome location: 6q22.31

miRNA

miRTarBase ID	miRNA	Experiments	Reference
MIRT982423	hsa-miR-128	CLIP-seq
MIRT982424	hsa-miR-27a	CLIP-seq
MIRT982425	hsa-miR-27b	CLIP-seq
MIRT982426	hsa-miR-489	CLIP-seq
MIRT982427	hsa-miR-513a-5p	CLIP-seq
MIRT982428	hsa-miR-514	CLIP-seq
MIRT982429	hsa-miR-514b-3p	CLIP-seq
MIRT2225330	hsa-miR-3671	CLIP-seq
MIRT2225331	hsa-miR-371-5p	CLIP-seq
MIRT2225332	hsa-miR-371b-5p	CLIP-seq
MIRT2225333	hsa-miR-4699-3p	CLIP-seq
MIRT2528925	hsa-miR-1236	CLIP-seq
MIRT2528926	hsa-miR-132	CLIP-seq
MIRT2528927	hsa-miR-212	CLIP-seq
MIRT2225330	hsa-miR-3671	CLIP-seq
MIRT2225331	hsa-miR-371-5p	CLIP-seq
MIRT2225332	hsa-miR-371b-5p	CLIP-seq
MIRT2528928	hsa-miR-548c-3p	CLIP-seq
MIRT2528925	hsa-miR-1236	CLIP-seq
MIRT2225330	hsa-miR-3671	CLIP-seq
MIRT2225331	hsa-miR-371-5p	CLIP-seq
MIRT2225332	hsa-miR-371b-5p	CLIP-seq
MIRT2528928	hsa-miR-548c-3p	CLIP-seq

Gene ontology (GO)

GO ID	Ontology	Definition	Evidence	Reference
GO:0000932	Component	P-body	IDA	33957083
GO:0000932	Component	P-body	IEA
GO:0005515	Function	Protein binding	IPI	24407287, 32296183, 32814053
GO:0005615	Component	Extracellular space	HDA	22664934
GO:0005737	Component	Cytoplasm	IEA
GO:0005829	Component	Cytosol	IDA
GO:0005856	Component	Cytoskeleton	IEA
GO:0034451	Component	Centriolar satellite	IDA	33957083
GO:0034451	Component	Centriolar satellite	IEA
GO:0036064	Component	Ciliary basal body	IDA

Other IDs

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

Protein

• UniProt ID: Q8NB25
• Protein name: Protein FAM184A
• Family and domains:

  Pfam

  Accession	ID	Position in sequence	Description	Type
  PF15665	FAM184	54 → 264	Family with sequence similarity 184, A and B	Coiled-coil

• Sequence:

  MATPGMSWQQHYYGGSAAKFAPSPATAQLAGHSMDYSQEMHLKMSKKIAQLTKVIYALNT
  KNDEHESAIQALKDAHEEEIQQILAETREKILQYKSKVTEELDLRRKIQVLESSLEDHIK
  MKQQALTEFEAYKHRVEDMQLCAEAQHVQRIVTMSREVEEIRRKFEEKLRSFGQLQVQFE
  KDKRLALEDLQAAHRREIQELLKSQQDHSASVNKGQEKAEELHRMEVESLNKMLEELRLE
  RKKLIEDYEGKLNKAQSFYERELDTLKRSQLFTAESLQASKEKEADLRKEFQGQEAILRK
  TIGKLKTELQMVQDEAGSLLDKCQKLQTALAIAENNVQVLQKQLDDAKEGEMALLSKHKE
  VESELAAARERLQQQASDLVLKASHIGMLQATQMTQEVTIKDLESEKSRVNERLSQLEEE
  RAFLRSKTQSLDEEQKQQILELEKKVNEAKRTQQEYYERELKNLQSRLEEEVTQLNEAHS
  KTLEELAWKHHMAIEAVHSNAIRDKKKLQMDLEEQHNKDKLNLEEDKNQLQQELENLKEV
  LEDKLNTANQEIGHLQDMVRKSEQGLGSAEGLIASLQDSQERLQNELDLTKDSLKETKDA
  LLNVEGELEQERQQHEETIAAMKEEEKLKVDKMAHDLEIKWTENLRQECSKLREELRLQH
  EEDKKSAMSQLLQLKDREKNAARDSWQKKVEDLLNQISLLKQNLEIQLSQSQTSLQQLQA
  QFTQERQRLTQELEELEEQHQQRHKSLKEAHVLAFQTMEEEKEKEQRALENHLQQKHSAE
  LQSLKDAHRESMEGFRIEMEQELQTLRFELEDEGKAMLASLRSELNHQHAAAIDLLRHNH
  HQELAAAKMELERSIDISRRQSKEHICRITDLQEELRHREHHISELDKEVQHLHENISAL
  TKELEFKGKEILRIRSESNQQIRLHEQDLNKRLEKELDVMTADHLREKNIMRADFNKTNE
  LLKEINAALQVSLEEMEEKYLMRESKPEDIQMITELKAMLTERDQIIKKLIEDNKFYQLE
  LVNRETNFNKVFNSSPTVGVINPLAKQKKKNDKSPTNRFVSVPNLSALESGGVGNGHPNR
  LDPIPNSPVHDIEFNSSKPLPQPVPPKGPKTFLSPAQSEASPVASPDPQRQEWFARYFTF
  

• Sequence length: 1140

Associated diseases

Unknown
Phenotype Name	Clinical Significance	dbSNP ID	RCV Accession
Melanoma	Uncertain significance	rs756769671	RCV005928901