C19orf73 (chromosome 19 open reading frame 73)

Gene

• Entrez ID: 55150
• Gene name: Chromosome 19 open reading frame 73
• Gene symbol: C19orf73
• Synonyms (NCBI Gene): -
• Chromosome: 19
• Chromosome location: 19q13.33

miRNA

miRTarBase ID	miRNA	Experiments	Reference
MIRT018765	hsa-miR-335-5p	Microarray	18185580
MIRT839030	hsa-miR-151-5p	CLIP-seq
MIRT839031	hsa-miR-151b	CLIP-seq
MIRT839032	hsa-miR-1972	CLIP-seq
MIRT839033	hsa-miR-28-5p	CLIP-seq
MIRT839034	hsa-miR-3139	CLIP-seq
MIRT839035	hsa-miR-3160-3p	CLIP-seq
MIRT839036	hsa-miR-4650-5p	CLIP-seq
MIRT839037	hsa-miR-4737	CLIP-seq
MIRT839038	hsa-miR-708	CLIP-seq
MIRT2445314	hsa-miR-3145-3p	CLIP-seq
MIRT2445315	hsa-miR-4725-5p	CLIP-seq
MIRT2445316	hsa-miR-504	CLIP-seq

Gene ontology (GO)

GO ID	Ontology	Definition	Evidence	Reference
GO:0005515	Function	Protein binding	IPI	25416956

Other IDs

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

Protein

• UniProt ID: Q9NVV2
• Protein name: Putative uncharacterized protein C19orf73
• Family and domains:

  Pfam

  Accession	ID	Position in sequence	Description	Type
  PF17692	DUF5538	1 → 128	Family of unknown function (DUF5538)	Family

• Sequence:

  MRLKVGFQGGGCFRKDALCLEGGVSARWARAPHSAPLRPPRELHAAPPPATPTQTVVRPA
  GFPRRTRLMVRSAPPTQRPPTGSGCVSGLWRKGLGLRPQTLLRVGSVVLSSAPALRPRLG
  PCLRPPPSD

• Sequence length: 129

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
METABOLIC SYNDROME	—	GWAS catalog	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
TYPE 2 DIABETES MELLITUS	—	GWAS catalog	★★☆☆☆ Found in Text Mining + Unknown/Other Associations