Gene Gene information from NCBI Gene database.
Entrez ID 26502
Gene name Nuclear prelamin A recognition factor
Gene symbol NARF
Synonyms (NCBI Gene)
IOP2
Chromosome 17
Chromosome location 17q25.3
Summary Several proteins have been found to be prenylated and methylated at their carboxyl-terminal ends. Prenylation was initially believed to be important only for membrane attachment. However, another role for prenylation appears to be its importance in protei
miRNA miRNA information provided by mirtarbase database.
135
miRTarBase ID miRNA Experiments Reference
MIRT027539 hsa-miR-98-5p Microarray 19088304
MIRT030389 hsa-miR-24-3p Microarray 19748357
MIRT031638 hsa-miR-16-5p Microarray 21199864
MIRT042570 hsa-miR-423-3p CLASH 23622248
MIRT701553 hsa-miR-508-5p HITS-CLIP 23313552
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
9
GO ID Ontology Definition Evidence Reference
GO:0005521 Function Lamin binding IBA
GO:0005521 Function Lamin binding IPI 10514485
GO:0005634 Component Nucleus IEA
GO:0005638 Component Lamin filament IBA
GO:0005638 Component Lamin filament IDA 10514485
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
605349 29916 ENSG00000141562
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9UHQ1
Protein name Nuclear prelamin A recognition factor (Iron-only hydrogenase-like protein 2) (IOP2)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02906 Fe_hyd_lg_C 92 382 Iron only hydrogenase large subunit, C-terminal domain Domain
PF02256 Fe_hyd_SSU 393 445 Iron hydrogenase small subunit Domain
Tissue specificity TISSUE SPECIFICITY: Ubiquitous. Predominantly expressed in skeletal muscle, heart and brain. {ECO:0000269|PubMed:10514485}.
Sequence
Sequence length 456
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
OSTEONECROSIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Breast Neoplasms Associate 37768037
★☆☆☆☆
Found in Text Mining only
Hypoxia Stimulate 37768037
★☆☆☆☆
Found in Text Mining only
Hypoxia Brain Associate 37768037
★☆☆☆☆
Found in Text Mining only