ACAD11 (acyl-CoA dehydrogenase family member 11)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 84129 |
| Gene name | Acyl-CoA dehydrogenase family member 11 |
| Gene symbol | ACAD11 |
| Synonyms (NCBI Gene) |
ACAD-11
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| Chromosome | 3 |
| Chromosome location | 3q22.1 |
| Summary | This gene encodes an acyl-CoA dehydrogenase enzyme with a preference for carbon chain lengths between 20 and 26. Naturally occurring read-through transcription occurs between the upstream gene NPHP3 (nephronophthisis 3 (adolescent)) and this gene. [provid |
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miRNA
miRNA information provided by mirtarbase database.
81
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
26
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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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Q709F0 | |||||||||||||||||||||||||
| Protein name | Acyl-CoA dehydrogenase family member 11 (ACAD-11) (EC 1.3.8.-) | |||||||||||||||||||||||||
| Protein function | Acyl-CoA dehydrogenase, that exhibits maximal activity towards saturated C22-CoA (PubMed:21237683). Probably participates in beta-oxydation and energy production but could also play a role in the metabolism of specific fatty acids to control fat | |||||||||||||||||||||||||
| PDB | 2WBI | |||||||||||||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Widely expressed with highest levels in brain followed by liver, heart and kidney. {ECO:0000269|PubMed:21237683}. | |||||||||||||||||||||||||
| Sequence |
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| Sequence length | 780 | |||||||||||||||||||||||||
| 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.).
3
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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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