Gene Gene information from NCBI Gene database.
Entrez ID 375287
Gene name RNA binding motif protein 43
Gene symbol RBM43
Synonyms (NCBI Gene)
C2orf38
Chromosome 2
Chromosome location 2q23.3
miRNA miRNA information provided by mirtarbase database.
466
miRTarBase ID miRNA Experiments Reference
MIRT018448 hsa-miR-335-5p Microarray 18185580
MIRT633695 hsa-miR-6819-3p HITS-CLIP 23824327
MIRT633694 hsa-miR-6877-3p HITS-CLIP 23824327
MIRT626255 hsa-miR-4722-3p HITS-CLIP 23824327
MIRT626254 hsa-miR-6727-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
3
GO ID Ontology Definition Evidence Reference
GO:0003676 Function Nucleic acid binding IEA
GO:0003723 Function RNA binding IEA
GO:0005515 Function Protein binding IPI 32296183
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.
Q6ZSC3
Protein name RNA-binding protein 43 (RNA-binding motif protein 43)
Family and domains
Sequence
MASVLNVKESKAPERTVVVAGLPVDLFSDQLLAVLVKSHFQDIKNEGGDVEDVIYPTRTK
GVAYVIFKEKKVAENVIRQKKHWLARKTRHAELTVSLRVSHFGDKIFSSVNAILDLSVFG
KEVTLETLVKDLKKKIPSLSFSPLKPNGRISVEGSFLAVKRLRESLLARACSLLEKDRNF
TSEERKWNRQNPQRNLQRSNNSLASVRTLVPETARSGEMLVLDTDVFLYLKHKCGSYEST
LKKFHILSQEKVDGEITTICLKSIQVGSQPNNAKHVKELIEEWSHALYLKLRKETFILEG
KENREKRMIKRACEQLSSRYLEVLINLYRTHIDIIGSSSDTYLFKKGVMKLIGQKVS
Sequence length 357
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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
CROHN'S DISEASE 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
Adenocarcinoma Of Esophagus Esophageal Cancer BEFREE 29551738
★☆☆☆☆
Found in Text Mining only
Brain Ischemia Brain ischemia Pubtator 32160184 Stimulate
★☆☆☆☆
Found in Text Mining only
Carotid Artery Diseases Carotid artery disease Pubtator 32160184 Associate
★☆☆☆☆
Found in Text Mining only
Endometriosis Endometriosis Pubtator 23472165 Associate
★☆☆☆☆
Found in Text Mining only
Esophageal Squamous Cell Carcinoma Esophageal squamous cell carcinoma Pubtator 34398362 Stimulate
★☆☆☆☆
Found in Text Mining only
Gastroesophageal Reflux Gastroesophageal reflux disease Pubtator 29551738 Associate
★☆☆☆☆
Found in Text Mining only
Gastroesophageal reflux disease Gastroesophageal Reflux Disease BEFREE 29551738
★☆☆☆☆
Found in Text Mining only