Gene Gene information from NCBI Gene database.
Entrez ID 317671
Gene name Rieske Fe-S domain containing
Gene symbol RFESD
Synonyms (NCBI Gene)
-
Chromosome 5
Chromosome location 5q15
miRNA miRNA information provided by mirtarbase database.
36
miRTarBase ID miRNA Experiments Reference
MIRT1301673 hsa-miR-24 CLIP-seq
MIRT1301674 hsa-miR-3133 CLIP-seq
MIRT1301675 hsa-miR-4284 CLIP-seq
MIRT1301676 hsa-miR-4420 CLIP-seq
MIRT1301677 hsa-miR-4427 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
5
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25416956, 31515488, 32296183
GO:0046872 Function Metal ion binding IEA
GO:0051536 Function Iron-sulfur cluster binding IEA
GO:0051537 Function 2 iron, 2 sulfur cluster binding IBA
GO:0051537 Function 2 iron, 2 sulfur cluster binding IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8TAC1
Protein name Rieske domain-containing protein
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00355 Rieske 16 109 Rieske [2Fe-2S] domain Domain
Sequence
MNLDGSAQDPEKREYSSVCVGREDDIKKSERMTAVVHDREVVIFYHKGEYHAMDIRCYHS
GGPLHLGDIEDFDGRPCIVCPWHKYKITLATGEGLYQSINPKDPSAKPK
WCSKGIKQRIH
TVTVDNGNIYVTLSNEPFKCDSDFYATGDFKVIKSSS
Sequence length 157
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
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
CARDIAC EMBOLISM GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CARDIOEMBOLIC STROKE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SQUAMOUS CELL LUNG CARCINOMA 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
Autism Spectrum Disorder Autism Pubtator 33159718 Associate
★☆☆☆☆
Found in Text Mining only
Bipolar Disorder Bipolar Disorder GWASCAT_DG 25944848
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Hepatocellular carcinoma Pubtator 35681134 Associate
★☆☆☆☆
Found in Text Mining only
Major Depressive Disorder Mental Depression GWASCAT_DG 25944848
★☆☆☆☆
Found in Text Mining only
Schizophrenia Schizophrenia GWASCAT_DG 25944848
★☆☆☆☆
Found in Text Mining only
Unipolar Depression Mental Depression GWASCAT_DG 25944848
★☆☆☆☆
Found in Text Mining only