Gene Gene information from NCBI Gene database.
Entrez ID 4682
Gene name NUBP iron-sulfur cluster assembly factor 1, cytosolic
Gene symbol NUBP1
Synonyms (NCBI Gene)
CIAO5NBPNBP1NBP35
Chromosome 16
Chromosome location 16p13.13
Summary NUBP1 is a member of the NUBP/MRP subfamily of ATP-binding proteins (Nakashima et al., 1999 [PubMed 10486206]).[supplied by OMIM, Mar 2008]
miRNA miRNA information provided by mirtarbase database.
55
miRTarBase ID miRNA Experiments Reference
MIRT020454 hsa-miR-106b-5p Microarray 17242205
MIRT048800 hsa-miR-93-5p CLASH 23622248
MIRT042522 hsa-miR-423-3p CLASH 23622248
MIRT039853 hsa-miR-615-3p CLASH 23622248
MIRT573118 hsa-miR-1203 PAR-CLIP 20371350
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
31
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0000166 Function Nucleotide binding TAS 7926816
GO:0001558 Process Regulation of cell growth IMP 18573874
GO:0005515 Function Protein binding IPI 18573874, 33961781
GO:0005524 Function ATP binding IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
600280 8041 ENSG00000103274
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P53384
Protein name Cytosolic Fe-S cluster assembly factor NUBP1 (Nucleotide-binding protein 1) (NBP 1)
Protein function Component of the cytosolic iron-sulfur (Fe/S) protein assembly (CIA) machinery (PubMed:18573874). Required for maturation of extramitochondrial Fe-S proteins (PubMed:18573874). The NUBP1-NUBP2 heterotetramer forms a Fe-S scaffold complex, mediat
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF10609 ParA 52 304 NUBPL iron-transfer P-loop NTPase Family
Sequence
Sequence length 320
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
4
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
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
COLOR VISION DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Gastric cancer Likely benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Melanoma Likely benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations