APOBEC4 (apolipoprotein B mRNA editing enzyme catalytic polypeptide like 4)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 403314 |
| Gene name | Apolipoprotein B mRNA editing enzyme catalytic polypeptide like 4 |
| Gene symbol | APOBEC4 |
| Synonyms (NCBI Gene) |
C1orf169
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| Chromosome | 1 |
| Chromosome location | 1q25.3 |
| Summary | This gene encodes a member of the AID/APOBEC family of polynucleotide (deoxy)cytidine deaminases, which convert cytidine to uridine. Other AID/APOBEC family members are involved in mRNA editing, somatic hypermutation and recombination of immunoglobulin ge |
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miRNA
miRNA information provided by mirtarbase database.
55
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
4
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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Q8WW27 | ||||||||||
| Protein name | Putative C->U-editing enzyme APOBEC-4 (EC 3.5.4.-) (Apolipoprotein B mRNA-editing enzyme catalytic polypeptide-like 4) | ||||||||||
| Protein function | Putative C to U editing enzyme whose physiological substrate is not yet known. | ||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Predominantly expressed in testis. {ECO:0000269|PubMed:16082223}. | ||||||||||
| Sequence |
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| Sequence length | 367 | ||||||||||
| Interactions | View interactions | ||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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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)
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