Gene Gene information from NCBI Gene database.
Entrez ID 81689
Gene name Iron-sulfur cluster assembly 1
Gene symbol ISCA1
Synonyms (NCBI Gene)
HBLD2ISA1MMDS5hIscAhIscA1
Chromosome 9
Chromosome location 9q21.33
Summary ISCA1 is a mitochondrial protein involved in the biogenesis and assembly of iron-sulfur clusters, which play a role in electron-transfer reactions (Cozar-Castellano et al., 2004 [PubMed 15262227]).[supplied by OMIM, Mar 2008]
SNPs SNP information provided by dbSNP.
2
SNP ID Visualize variation Clinical significance Consequence
rs776679653 C>T Pathogenic Coding sequence variant, missense variant
rs1587823007 A>C Pathogenic Missense variant, coding sequence variant
miRNA miRNA information provided by mirtarbase database.
262
miRTarBase ID miRNA Experiments Reference
MIRT047223 hsa-miR-181c-5p CLASH 23622248
MIRT563453 hsa-miR-4311 PAR-CLIP 20371350
MIRT563452 hsa-miR-1276 PAR-CLIP 20371350
MIRT563451 hsa-miR-583 PAR-CLIP 20371350
MIRT563449 hsa-miR-6499-3p PAR-CLIP 20371350
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
13
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25347204, 33961781
GO:0005737 Component Cytoplasm IBA
GO:0005739 Component Mitochondrion HTP 34800366
GO:0005739 Component Mitochondrion IBA
GO:0005739 Component Mitochondrion IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
611006 28660 ENSG00000135070
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9BUE6
Protein name Iron-sulfur cluster assembly 1 homolog, mitochondrial (HESB-like domain-containing protein 2) (Iron-sulfur assembly protein IscA) (hIscA)
Protein function Involved in the maturation of mitochondrial 4Fe-4S proteins functioning late in the iron-sulfur cluster assembly pathway. Probably involved in the binding of an intermediate of Fe/S cluster assembly. {ECO:0000269|PubMed:15262227, ECO:0000269|Pub
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01521 Fe-S_biosyn 23 125 Iron-sulphur cluster biosynthesis Family
Tissue specificity TISSUE SPECIFICITY: Detected in cerebellum, kidney and heart. {ECO:0000269|PubMed:15262227}.
Sequence
Sequence length 129
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Mitochondrial iron-sulfur cluster biogenesis
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
5
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Multiple mitochondrial dysfunctions syndrome 5 Pathogenic rs1587823007 RCV000857321
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Fatal multiple mitochondrial dysfunctions syndrome Conflicting classifications of pathogenicity rs776679653 RCV000508655
ISCA1-related disorder Likely benign rs997344571 RCV003934743
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Carcinogenesis Associate 36072584
Carcinoma Renal Cell Associate 36385109
Mitochondrial Diseases Associate 28356563
Multiple Mitochondrial Dysfunctions Syndrome Associate 28356563, 36385109
Neoplasms Associate 36072584, 39766805
Thyroid Neoplasms Associate 39766805
Urinary Bladder Neoplasms Associate 36072584