Gene Gene information from NCBI Gene database.
Entrez ID 160140
Gene name Chromosome 11 open reading frame 65
Gene symbol C11orf65
Synonyms (NCBI Gene)
MFI
Chromosome 11
Chromosome location 11q22.3
SNPs SNP information provided by dbSNP.
1
SNP ID Visualize variation Clinical significance Consequence
rs11212617 C>A Drug-response Intron variant
miRNA miRNA information provided by mirtarbase database.
2
miRTarBase ID miRNA Experiments Reference
MIRT018726 hsa-miR-335-5p Microarray 18185580
MIRT021504 hsa-miR-145-5p Reporter assay;Microarray 21351259
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
12
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25416956, 32296183, 32814053
GO:0005737 Component Cytoplasm IEA
GO:0005739 Component Mitochondrion IEA
GO:0005741 Component Mitochondrial outer membrane IEA
GO:0005741 Component Mitochondrial outer membrane ISS
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.
Q8NCR3
Protein name Protein MFI (Mitochondrial fission factor interactor)
Protein function Acts as an inhibitor of mitochondrial fission. Interacts with MFF and prevents DNM1L recruitment to mitochondria, promoting a more fused mitochondrial network.
Family and domains
Tissue specificity TISSUE SPECIFICITY: Enriched in the pancreatic beta cell and the testis and is expressed at low levels in other tissues tested. {ECO:0000269|PubMed:30059978}.
Sequence
MPWKEESEFTKQDKAARVIQQAWKSFLNVAIFQHFKSLIDLRRQGEPRQIVKYINPKEAE
LLDAAAGIHVRFRLGGVKFPPDIYYKIFTHRPIEDLCANSPRNYAKLPAKHTSHNKNDHL
QEEDHSGWYHRIENNGWRPVSDTFWLSTDGMVVEDKKESEFHFSKLKRRQDLEKKRKLRK
IEWMRQMYYSGSLEAKSTHHETLGLIHTATKGLIRAFEDGGIDSVMEWEVDEVLNWTNTL
NFDEYIASWKEIATSNSSANFKGFRFNQAQKNIYNYGGDISKMQMGIPDDTYYENVYQEP
NVTRLTPDSTYGL
Sequence length 313
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
35
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 Evidence Score
ATAXIA TELANGIECTASIA Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ATAXIA-TELANGIECTASIA VARIANT Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BASAL CELL CARCINOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BILIARY TRACT CANCER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Adenoma Associate 21504893
★☆☆☆☆
Found in Text Mining only
Colorectal Neoplasms Associate 32408300
★☆☆☆☆
Found in Text Mining only
Coronary Artery Disease Associate 24281401
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus Type 2 Associate 22751958
★☆☆☆☆
Found in Text Mining only
HIV Infections Associate 23171036
★☆☆☆☆
Found in Text Mining only
Inflammation Associate 23171036
★☆☆☆☆
Found in Text Mining only
Insulin Resistance Associate 23171036
★☆☆☆☆
Found in Text Mining only