Gene Gene information from NCBI Gene database.
Entrez ID 30010
Gene name Neurexophilin 1
Gene symbol NXPH1
Synonyms (NCBI Gene)
NPH1Nbla00697
Chromosome 7
Chromosome location 7p21.3
Summary This gene is a member of the neurexophilin family and encodes a secreted protein with a variable N-terminal domain, a highly conserved, N-glycosylated central domain, a short linker region, and a cysteine-rich C-terminal domain. This protein forms a very
miRNA miRNA information provided by mirtarbase database.
89
miRTarBase ID miRNA Experiments Reference
MIRT1200546 hsa-let-7a CLIP-seq
MIRT1200547 hsa-let-7b CLIP-seq
MIRT1200548 hsa-let-7c CLIP-seq
MIRT1200549 hsa-let-7d CLIP-seq
MIRT1200550 hsa-let-7e 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:0005102 Function Signaling receptor binding IBA
GO:0005102 Function Signaling receptor binding IEA
GO:0005576 Component Extracellular region IEA
GO:0043083 Component Synaptic cleft 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
604639 20693 ENSG00000122584
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P58417
Protein name Neurexophilin-1
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 63 271 Neurexophilin Family
Sequence
Sequence length 271
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
20
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
BINGE EATING GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BIPOLAR DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BREAST CARCINOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
COLOR VISION DISORDER 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
Alzheimer Disease Alzheimer disease Pubtator 20100581 Associate
★☆☆☆☆
Found in Text Mining only
Autism Spectrum Disorders Autism Spectrum Disorder BEFREE 22016809
★☆☆☆☆
Found in Text Mining only
Autistic Disorder Autism Pubtator 22016809 Associate
★☆☆☆☆
Found in Text Mining only
Chronic kidney disease stage 5 Kidney Disease BEFREE 8995741
★☆☆☆☆
Found in Text Mining only
Dandy-Walker Syndrome Dandy-Walker Syndrome BEFREE 10511339
★☆☆☆☆
Found in Text Mining only
Depressive disorder Mental Depression BEFREE 24041540
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus Diabetes mellitus Pubtator 28068899 Associate
★☆☆☆☆
Found in Text Mining only
Familial aplasia of the vermis Cerebellar vermis agenesis BEFREE 10511339
★☆☆☆☆
Found in Text Mining only
Hydrocephalus, Normal Pressure Hydrocephalus BEFREE 7806215, 8995741, 9502560, 9587065
★☆☆☆☆
Found in Text Mining only
Intellectual Disability Mental retardation BEFREE 17601928
★☆☆☆☆
Found in Text Mining only