C1orf87 (chromosome 1 open reading frame 87)

Gene Gene information from NCBI Gene database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Entrez ID 127795
Gene name Chromosome 1 open reading frame 87
Gene symbol C1orf87
Synonyms (NCBI Gene)
CREF
Chromosome 1
Chromosome location 1p32.1
miRNA miRNA information provided by mirtarbase database.
94
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all (94)
miRTarBase ID miRNA Experiments Reference
MIRT616392 hsa-miR-4714-5p HITS-CLIP 23824327
MIRT616391 hsa-miR-22-3p HITS-CLIP 23824327
MIRT616390 hsa-miR-6777-3p HITS-CLIP 23824327
MIRT616388 hsa-miR-1234-3p HITS-CLIP 23824327
MIRT616389 hsa-miR-7107-5p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
2
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all (2)
GO ID Ontology Definition Evidence Reference
GO:0005929 Component Cilium IDA 28282151
GO:0005930 Component Axoneme IDA 28282151
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
618860 28547 ENSG00000162598
Protein Protein information from UniProt database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8N0U7
Protein name Uncharacterized protein C1orf87
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF17743 DUF5580 1 → 546 Family of unknown function (DUF5580) Family
Sequence
Sequence length 546
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
4
Gene miRNA Gene ontology Other IDs Protein 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)
Show/Hide Unknown Diseases (4)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
CENTRAL NERVOUS SYSTEM CANCER — GWAS catalog
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
DYSLEXIA — GWAS catalog
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
GLIOMA — GWAS catalog
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MIGRAINE DISORDER — GWAS catalog
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Show/Hide Text Mining Associations (2)
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Malignant neoplasm of breast Breast Cancer UNIPROT_DG
★★★★★
★☆☆☆☆
Found in Text Mining only
Neoplasms Neoplasms BEFREE 1580547
★★★★★
★☆☆☆☆
Found in Text Mining only