Gene Gene information from NCBI Gene database.
Entrez ID 11247
Gene name Neurexophilin 4
Gene symbol NXPH4
Synonyms (NCBI Gene)
NPH4
Chromosome 12
Chromosome location 12q13.3
miRNA miRNA information provided by mirtarbase database.
72
miRTarBase ID miRNA Experiments Reference
MIRT030127 hsa-miR-26b-5p Microarray 19088304
MIRT037557 hsa-miR-744-5p CLASH 23622248
MIRT037557 hsa-miR-744-5p CLASH 23622248
MIRT1200699 hsa-miR-1245b-5p CLIP-seq
MIRT1200700 hsa-miR-1254 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
6
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
GO:0045202 Component Synapse IEA
GO:0050804 Process Modulation of chemical synaptic transmission IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
604637 8078 ENSG00000182379
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O95158
Protein name Neurexophilin-4
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 69 166 Neurexophilin Family
PF06312 Neurexophilin 221 308 Neurexophilin Family
Tissue specificity TISSUE SPECIFICITY: Expressed in brain, spleen, and testis.
Sequence
Sequence length 308
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
TYPE 2 DIABETES MELLITUS GWAS catalog
★★☆☆☆
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
Arthritis, Gouty Gouty arthritis GWASDB_DG 23263486
★☆☆☆☆
Found in Text Mining only
Autosomal dominant compelling helio ophthalmic outburst syndrome Achoo syndrome GWASCAT_DG 27182965
★☆☆☆☆
Found in Text Mining only
Colorectal Neoplasms Colorectal neoplasm Pubtator 38613793 Associate
★☆☆☆☆
Found in Text Mining only
Gout Gout GWASDB_DG 23263486
★☆☆☆☆
Found in Text Mining only
Urinary Bladder Neoplasms Urinary bladder neoplasms Pubtator 35462469, 35758021 Associate
★☆☆☆☆
Found in Text Mining only