Gene Gene information from NCBI Gene database.
Entrez ID 29989
Gene name Odorant binding protein 2B
Gene symbol OBP2B
Synonyms (NCBI Gene)
LCN14OBPIIb
Chromosome 9
Chromosome location 9q34.2
miRNA miRNA information provided by mirtarbase database.
7
miRTarBase ID miRNA Experiments Reference
MIRT1201663 hsa-miR-3155 CLIP-seq
MIRT1201664 hsa-miR-3155b CLIP-seq
MIRT1201665 hsa-miR-323-5p CLIP-seq
MIRT1201666 hsa-miR-4645-5p CLIP-seq
MIRT1201667 hsa-miR-4673 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
7
GO ID Ontology Definition Evidence Reference
GO:0005549 Function Odorant binding NAS 10607840
GO:0005576 Component Extracellular region IEA
GO:0005615 Component Extracellular space IBA
GO:0007608 Process Sensory perception of smell IEA
GO:0007608 Process Sensory perception of smell NAS 10607840
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
604606 23381 ENSG00000171102
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NPH6
Protein name Odorant-binding protein 2b (Odorant-binding protein IIb) (OBPIIb)
Protein function Probably binds and transports small hydrophobic volatile molecules.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00061 Lipocalin 26 164 Lipocalin / cytosolic fatty-acid binding protein family Domain
Tissue specificity TISSUE SPECIFICITY: Strongly expressed in genital sphere organs such as the prostate and mammary glands.
Sequence
Sequence length 170
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
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
BREAST CANCER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
RHEUMATOID ARTHRITIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SYSTEMIC LUPUS ERYTHEMATOSUS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Alzheimer Disease Associate 37895183
★☆☆☆☆
Found in Text Mining only
Glaucoma Associate 39342991
★☆☆☆☆
Found in Text Mining only
Sleep Apnea Obstructive Associate 34529670
★☆☆☆☆
Found in Text Mining only
Stomach Neoplasms Associate 33795748
★☆☆☆☆
Found in Text Mining only
Venous Thromboembolism Associate 37537391
★☆☆☆☆
Found in Text Mining only