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Gene Gene information from NCBI Gene database.
Entrez ID 79074
Gene name Chromosome 2 open reading frame 49
Gene symbol C2orf49
Synonyms (NCBI Gene)
asw
Chromosome 2
Chromosome location 2q12.2
miRNA miRNA information provided by mirtarbase database.
160 Show/Hide all (160)
miRTarBase ID miRNA Experiments Reference
MIRT026435 hsa-miR-192-5p Microarray 19074876
MIRT519136 hsa-miR-6796-3p HITS-CLIP 21572407
MIRT519135 hsa-miR-5580-3p HITS-CLIP 21572407
MIRT510131 hsa-miR-5011-5p HITS-CLIP 21572407
MIRT519134 hsa-miR-600 HITS-CLIP 21572407
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
13 Show/Hide all (13)
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 30021884, 32814053, 33961781
GO:0005634 Component Nucleus IDA 18445686
GO:0005634 Component Nucleus IEA
GO:0005634 Component Nucleus NAS 21311021
GO:0005654 Component Nucleoplasm IDA
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.
Q9BVC5
Protein name Ashwin
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15323 Ashwin 13 → 232 Developmental protein Family
Sequence
Sequence length 232
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
Reactome Pathway
tRNA processing in the nucleus
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
7
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 (7)
Phenotype Name Clinical Significance Source Reference Evidence Score
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA — Disgenet —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ATTENTION DEFICIT HYPERACTIVITY DISORDER — GWAS catalog 34446935
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CARDIOMYOPATHIES — Disgenet —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CARDIOMYOPATHY, DILATED — Disgenet —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CARDIOMYOPATHY, HYPERTROPHIC, FAMILIAL — Disgenet —
★★★★★
★★☆☆☆
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
Dermatitis, Atopic Dermatitis BEFREE 29791750
★★★★★
★☆☆☆☆
Found in Text Mining only
Eczema Eczema BEFREE 29791750
★★★★★
★☆☆☆☆
Found in Text Mining only