Gene Gene information from NCBI Gene database.
Entrez ID 56675
Gene name Nuclear receptor interacting protein 3
Gene symbol NRIP3
Synonyms (NCBI Gene)
C11orf14NY-SAR-105
Chromosome 11
Chromosome location 11p15.4
miRNA miRNA information provided by mirtarbase database.
633
miRTarBase ID miRNA Experiments Reference
MIRT021324 hsa-miR-9-5p Microarray 17612493
MIRT611450 hsa-miR-1306-5p HITS-CLIP 23824327
MIRT611449 hsa-miR-6511a-3p HITS-CLIP 23824327
MIRT611448 hsa-miR-6511b-3p HITS-CLIP 23824327
MIRT611447 hsa-miR-6784-3p 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:0004190 Function Aspartic-type endopeptidase activity IEA
GO:0005515 Function Protein binding IPI 25416956, 32296183
GO:0006508 Process Proteolysis IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
613125 1167 ENSG00000175352
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NQ35
Protein name Nuclear receptor-interacting protein 3 (Sarcoma antigen NY-SAR-105)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF09668 Asp_protease 87 209 Aspartyl protease Family
Sequence
MFYSGLLTEGGRKETDMREAASLRQQRRMKQAVQFIHKDSADLLPLDGLKKLGSSKDMQP
HNILQRRLMETNLSKLRSGPRVPWASKTNKLNQAKSEGLKKSEEDDMILVSCQCAGKDVK
ALVDTGCLYNLISLACVDRLGLKEHVKSHKHEGEKLSLPRHLKVVGQIEHLVITLGSLRL
DCPAAVVDDNEKNLSLGLQTLRSLKCIIN
LDKHRLIMGKTDKEEIPFVETVSLNEDNTSE
A
Sequence length 241
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
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations