Gene Gene information from NCBI Gene database.
Entrez ID 79892
Gene name Minichromosome maintenance complex binding protein
Gene symbol MCMBP
Synonyms (NCBI Gene)
C10orf119MCM-BP
Chromosome 10
Chromosome location 10q26.11
Summary This gene encodes a protein which is a component of the hexameric minichromosome maintenance (MCM) complex which regulates initiation and elongation of DNA. Multiple transcript variants encoding different isoforms have been found for this gene. [provided
miRNA miRNA information provided by mirtarbase database.
178
miRTarBase ID miRNA Experiments Reference
MIRT019649 hsa-miR-340-5p Sequencing 20371350
MIRT025386 hsa-miR-34a-5p Proteomics 21566225
MIRT029372 hsa-miR-26b-5p Microarray 19088304
MIRT044035 hsa-miR-365a-3p CLASH 23622248
MIRT042503 hsa-miR-423-3p CLASH 23622248
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
14
GO ID Ontology Definition Evidence Reference
GO:0003682 Function Chromatin binding IBA
GO:0003682 Function Chromatin binding IDA 17296731
GO:0005515 Function Protein binding IPI 17296731, 22540012, 24299456, 25036637, 25416956, 26871637, 32296183, 33961781
GO:0005634 Component Nucleus IDA 17296731
GO:0005634 Component Nucleus IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
610909 25782 ENSG00000197771
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9BTE3
Protein name Mini-chromosome maintenance complex-binding protein (MCM-BP) (MCM-binding protein)
Protein function Associated component of the MCM complex that acts as a regulator of DNA replication. Binds to the MCM complex during late S phase and promotes the disassembly of the MCM complex from chromatin, thereby acting as a key regulator of pre-replicatio
PDB 4KG9
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF09739 MCM_bind 36 631 Mini-chromosome maintenance replisome factor Family
Sequence
Sequence length 642
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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
MAJOR DEPRESSIVE DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Malignant tumor of urinary bladder 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
Colorectal Neoplasms Colorectal neoplasm Pubtator 25246271 Associate
★☆☆☆☆
Found in Text Mining only