Gene Gene information from NCBI Gene database.
Entrez ID 53838
Gene name Chromosome 11 open reading frame 24
Gene symbol C11orf24
Synonyms (NCBI Gene)
DM4E3
Chromosome 11
Chromosome location 11q13.2
miRNA miRNA information provided by mirtarbase database.
183
miRTarBase ID miRNA Experiments Reference
MIRT016402 hsa-miR-193b-3p Microarray 20304954
MIRT025652 hsa-miR-7-5p Microarray 19073608
MIRT568239 hsa-miR-25-3p PAR-CLIP 20371350
MIRT568238 hsa-miR-32-5p PAR-CLIP 20371350
MIRT568237 hsa-miR-363-3p PAR-CLIP 20371350
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
7
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0005654 Component Nucleoplasm IDA
GO:0005794 Component Golgi apparatus IBA
GO:0005794 Component Golgi apparatus IDA
GO:0005794 Component Golgi apparatus IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
610880 1174 ENSG00000171067
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96F05
Protein name Uncharacterized protein C11orf24 (Protein DM4E3)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF17823 DUF5585 1 449 Family of unknown function (DUF5585) Family
Tissue specificity TISSUE SPECIFICITY: Highest expression in heart, placenta, liver, pancreas and colon. Also detected in brain, lung, skeletal muscle, kidney, spleen, prostate, testis, ovary and small intestine. Lowest expression in thymus and leukocytes. {ECO:0000269|PubM
Sequence
Sequence length 449
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 Evidence Score
GOUT GWAS catalog
★★☆☆☆
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
Neutropenia Neutropenia Pubtator 40285634 Associate
★☆☆☆☆
Found in Text Mining only
Pancreatic Neoplasms Pancreatic neoplasm Pubtator 40285634 Associate
★☆☆☆☆
Found in Text Mining only