Gene Gene information from NCBI Gene database.
Entrez ID 11249
Gene name Neurexophilin 2
Gene symbol NXPH2
Synonyms (NCBI Gene)
NPH2
Chromosome 2
Chromosome location 2q22.1
miRNA miRNA information provided by mirtarbase database.
32
miRTarBase ID miRNA Experiments Reference
MIRT023595 hsa-miR-1-3p Microarray 18668037
MIRT051108 hsa-miR-16-5p CLASH 23622248
MIRT1200587 hsa-miR-1236 CLIP-seq
MIRT1200588 hsa-miR-3117-3p CLIP-seq
MIRT1200589 hsa-miR-3123 CLIP-seq
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:0005102 Function Signaling receptor binding IBA
GO:0005576 Component Extracellular region IEA
GO:0007218 Process Neuropeptide signaling pathway NAS 9570794
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
604635 8076 ENSG00000144227
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O95156
Protein name Neurexophilin-2
Protein function May be signaling molecules that resemble neuropeptides and that act by binding to alpha-neurexins and possibly other receptors.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF06312 Neurexophilin 52 264 Neurexophilin Family
Tissue specificity TISSUE SPECIFICITY: Expressed in brain and kidney.
Sequence
Sequence length 264
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
OVARIAN CYSTS CTD
★★☆☆☆
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
Carcinoma, Ovarian Epithelial Ovarian Epithelial carcinoma BEFREE 19304784
★☆☆☆☆
Found in Text Mining only
Corpus Luteum Cyst Corpus Luteum Cyst CTD_human_DG 21239663
★☆☆☆☆
Found in Text Mining only
Malignant neoplasm of ovary Ovarian cancer BEFREE 19304784
★☆☆☆☆
Found in Text Mining only
NEPHRONOPHTHISIS 2 Nephronophthisis GENOMICS_ENGLAND_DG
★☆☆☆☆
Found in Text Mining only
Ovarian Cysts Ovarian Cysts CTD_human_DG 21239663
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ovarian neoplasm Ovarian neoplasm BEFREE 19304784
★☆☆☆☆
Found in Text Mining only
Ovarian Neoplasms Ovarian neoplasm Pubtator 19304784 Associate
★☆☆☆☆
Found in Text Mining only