MKRN2OS (MKRN2 opposite strand)

Gene Gene information from NCBI Gene database.
Gene miRNA Other IDs Protein Associated diseases
Entrez ID 100129480
Gene name MKRN2 opposite strand
Gene symbol MKRN2OS
Synonyms (NCBI Gene)
C3orf83MKRN2-AS1
Chromosome 3
Chromosome location 3p25.2
miRNA miRNA information provided by mirtarbase database.
15
Gene miRNA Other IDs Protein Associated diseases
Show/Hide all (15)
miRTarBase ID miRNA Experiments Reference
MIRT741872 hsa-miR-1244 HITS-CLIP 23824327
MIRT741873 hsa-miR-4715-5p HITS-CLIP 23824327
MIRT741874 hsa-miR-4259 HITS-CLIP 23824327
MIRT741875 hsa-miR-325 HITS-CLIP 23824327
MIRT741876 hsa-miR-6778-3p HITS-CLIP 23824327
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
Gene miRNA Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
Gene miRNA Other IDs Protein Associated diseases
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
H3BPM6
Protein name MKRN2 opposite strand protein (MKRN2 antisense RNA 1) (MKRN2 antisense gene protein 1)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF16044 DUF4796 8 → 199 Domain of unknown function (DUF4796) Family
Sequence
Sequence length 223
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
Gene miRNA Other IDs Protein Associated diseases
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)
Show/Hide Unknown Diseases (2)
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
HYPERTROPHIC CARDIOMYOPATHY — GWAS catalog
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SYSTEMIC LUPUS ERYTHEMATOSUS — GWAS catalog
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Show/Hide Text Mining Associations (2)
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Pontocerebellar Hypoplasia Type 2A Pontoneocerebellar hypoplasia CLINVAR_DG
★★★★★
★☆☆☆☆
Found in Text Mining only
Pontocerebellar Hypoplasia Type 2B Pontoneocerebellar hypoplasia CLINVAR_DG
★★★★★
★☆☆☆☆
Found in Text Mining only