C20orf202 (chromosome 20 open reading frame 202)

Gene

• Entrez ID: 400831
• Gene name: Chromosome 20 open reading frame 202
• Gene symbol: C20orf202
• Synonyms (NCBI Gene): -
• Chromosome: 20
• Chromosome location: 20p13

miRNA

miRTarBase ID	miRNA	Experiments	Reference
MIRT843688	hsa-miR-1245b-3p	CLIP-seq
MIRT843689	hsa-miR-1275	CLIP-seq
MIRT843690	hsa-miR-1286	CLIP-seq
MIRT843691	hsa-miR-1343	CLIP-seq
MIRT843692	hsa-miR-186	CLIP-seq
MIRT843693	hsa-miR-3147	CLIP-seq
MIRT843694	hsa-miR-3616-3p	CLIP-seq
MIRT843695	hsa-miR-3914	CLIP-seq
MIRT843696	hsa-miR-3978	CLIP-seq
MIRT843697	hsa-miR-4292	CLIP-seq
MIRT843698	hsa-miR-4308	CLIP-seq
MIRT843699	hsa-miR-4425	CLIP-seq
MIRT843700	hsa-miR-4433	CLIP-seq
MIRT843701	hsa-miR-4436b-3p	CLIP-seq
MIRT843702	hsa-miR-4646-5p	CLIP-seq
MIRT843703	hsa-miR-4665-5p	CLIP-seq
MIRT843704	hsa-miR-4687-3p	CLIP-seq
MIRT843705	hsa-miR-4721	CLIP-seq
MIRT843706	hsa-miR-4722-5p	CLIP-seq
MIRT843707	hsa-miR-4747-5p	CLIP-seq
MIRT843708	hsa-miR-516a-3p	CLIP-seq
MIRT843709	hsa-miR-542-3p	CLIP-seq
MIRT843710	hsa-miR-7	CLIP-seq
MIRT843711	hsa-miR-875-3p	CLIP-seq
MIRT843712	hsa-miR-922	CLIP-seq
MIRT1949992	hsa-miR-1226	CLIP-seq
MIRT1949993	hsa-miR-197	CLIP-seq
MIRT1949994	hsa-miR-345	CLIP-seq
MIRT843695	hsa-miR-3914	CLIP-seq
MIRT1949995	hsa-miR-3919	CLIP-seq
MIRT843701	hsa-miR-4436b-3p	CLIP-seq
MIRT1949996	hsa-miR-4530	CLIP-seq
MIRT1949997	hsa-miR-4701-5p	CLIP-seq
MIRT1949998	hsa-miR-4733-5p	CLIP-seq
MIRT1949999	hsa-miR-4765	CLIP-seq
MIRT1950000	hsa-miR-5096	CLIP-seq
MIRT1950001	hsa-miR-588	CLIP-seq
MIRT1950002	hsa-miR-605	CLIP-seq
MIRT1950003	hsa-miR-634	CLIP-seq
MIRT2188071	hsa-miR-128	CLIP-seq
MIRT2188072	hsa-miR-203	CLIP-seq
MIRT2188073	hsa-miR-27a	CLIP-seq
MIRT2188074	hsa-miR-27b	CLIP-seq
MIRT2188075	hsa-miR-488	CLIP-seq

Gene ontology (GO)

GO ID	Ontology	Definition	Evidence	Reference
GO:0005515	Function	Protein binding	IPI	32296183

Other IDs

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

Protein

• UniProt ID: A1L168
• Protein name: Uncharacterized protein C20orf202
• Sequence:

  MYKSKIPRAQNQVSVKVTPKNTEMKIAEEPSPSLGQTLEWLRKELSEMQIQDQSLLLTLR
  HLHSVLEELRADSAHWEDARSSGGTSPIRARAGSEGRGCQPVCSRGLAQLLRGEDSRRSS
  LP

• Sequence length: 122

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
MULTIPLE SCLEROSIS	—	GWAS catalog	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
OLIGODENDROGLIOMA	—	GWAS catalog	★★☆☆☆ Found in Text Mining + Unknown/Other Associations