Log in to bookmark this gene

Bookmark This Gene

Gene Gene information from NCBI Gene database.
Entrez ID 51286
Gene name Cell cycle exit and neuronal differentiation 1
Gene symbol CEND1
Synonyms (NCBI Gene)
BM88
Chromosome 11
Chromosome location 11p15.5
Summary The protein encoded by this gene is a neuron-specific protein. The similar protein in pig enhances neuroblastoma cell differentiation in vitro and may be involved in neuronal differentiation in vivo. Multiple pseudogenes have been reported for this gene.
miRNA miRNA information provided by mirtarbase database.
58 Show/Hide all (58)
miRTarBase ID miRNA Experiments Reference
MIRT018322 hsa-miR-335-5p Microarray 18185580
MIRT029783 hsa-miR-26b-5p Microarray 19088304
MIRT053430 hsa-miR-512-5p Microarray 23807165
MIRT884582 hsa-miR-1207-5p CLIP-seq
MIRT884583 hsa-miR-1224-3p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
15 Show/Hide all (15)
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 30177828, 32296183
GO:0005739 Component Mitochondrion IDA 11311134
GO:0007628 Process Adult walking behavior IEA
GO:0016020 Component Membrane IEA
GO:0021549 Process Cerebellum development IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
608213 24153 ENSG00000184524
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8N111
Protein name Cell cycle exit and neuronal differentiation protein 1 (BM88 antigen)
Protein function Involved in neuronal differentiation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15677 CEND1 1 → 149 Cell cycle exit and neuronal differentiation protein 1 Family
Tissue specificity TISSUE SPECIFICITY: Neuron specific. {ECO:0000269|PubMed:11311134}.
Sequence
Sequence length 149
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
Familial cancer of breast Uncertain significance 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
Beckwith-Wiedemann Syndrome Beckwith-Wiedemann Syndrome BEFREE 11311134
★★★★★
★☆☆☆☆
Found in Text Mining only
Familial aplasia of the vermis Cerebellar vermis agenesis BEFREE 23658157
★★★★★
★☆☆☆☆
Found in Text Mining only
Global developmental delay Developmental Delay BEFREE 23658157
★★★★★
★☆☆☆☆
Found in Text Mining only
Neuroblastoma Neuroblastoma BEFREE 11311134
★★★★★
★☆☆☆☆
Found in Text Mining only