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Gene Gene information from NCBI Gene database.
Entrez ID 399947
Gene name Chromosome 11 open reading frame 87
Gene symbol C11orf87
Synonyms (NCBI Gene)
LOH11CR1ANEURIM1
Chromosome 11
Chromosome location 11q22.3
miRNA miRNA information provided by mirtarbase database.
120 Show/Hide all (120)
miRTarBase ID miRNA Experiments Reference
MIRT660064 hsa-miR-501-5p HITS-CLIP 23824327
MIRT660063 hsa-miR-6736-3p HITS-CLIP 23824327
MIRT660062 hsa-miR-4638-3p HITS-CLIP 23824327
MIRT660061 hsa-miR-4520-3p HITS-CLIP 23824327
MIRT660064 hsa-miR-501-5p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
2
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25416956, 32296183
GO:0016020 Component Membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6NUJ2
Protein name Uncharacterized protein C11orf87
Family and domains
Sequence
MSARAPKELRLALPPCLLNRTFASPNASGSGNTGARGPGAVGSGTCITQVGQQLFQSFSS
TLVLIVLVTLIFCLIVLSLSTFHIHKRRMKKRKMQRAQEEYERDHCSGSRGGGGLPRPGR
QAPTHAKETRLERQPRDSPFCAPSNASSLSSSSPGLPCQGPCAPPPPPPASSPQGAHAAS
SCLDTAGEGLLQTVVLS
Sequence length 197
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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 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 Reference Evidence Score
EBV-positive nodal T- and NK-cell lymphoma Likely benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Schizophrenia Schizophrenia Pubtator 31959813 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Stomach Neoplasms Stomach neoplasms Pubtator 33886682 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only