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Gene Gene information from NCBI Gene database.
Entrez ID 148362
Gene name BRO1 domain and CAAX motif containing
Gene symbol BROX
Synonyms (NCBI Gene)
C1orf58
Chromosome 1
Chromosome location 1q41
miRNA miRNA information provided by mirtarbase database.
293 Show/Hide all (293)
miRTarBase ID miRNA Experiments Reference
MIRT669865 hsa-miR-4318 HITS-CLIP 19536157
MIRT669864 hsa-miR-5693 HITS-CLIP 19536157
MIRT669863 hsa-miR-6499-3p HITS-CLIP 19536157
MIRT669862 hsa-miR-6076 HITS-CLIP 19536157
MIRT669861 hsa-miR-6797-3p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
7 Show/Hide all (7)
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 22162750, 22484091, 28514442, 33961781, 34818527
GO:0005634 Component Nucleus IEA
GO:0005635 Component Nuclear envelope IDA 34818527
GO:0007084 Process Mitotic nuclear membrane reassembly IMP 34818527
GO:0016020 Component Membrane 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.
Q5VW32
Protein name BRO1 domain-containing protein BROX (BRO1 domain- and CAAX motif-containing protein)
Protein function Nuclear envelope-associated factor that is involved in the nuclear envelope ruptures during interphase (NERDI) repair, where it is locally recruited by CHMP5 and reduces cytoskeletal stress through its action on SYN2 to help reseal the ruptured
PDB 3R9M , 3ULY , 3UM0 , 3UM1 , 3UM2 , 3UM3 , 3ZXP
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03097 BRO1 27 → 374 BRO1-like domain Domain
Sequence
Sequence length 411
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
9
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.
Show/Hide Unknown Diseases (9)
Phenotype Name Clinical Significance Source Reference Evidence Score
Acute myeloid leukemia Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Cervical cancer Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Clear cell carcinoma of kidney Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Colon adenocarcinoma Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Familial cancer of breast Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations