Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
30010
Gene name Gene Name - the full gene name approved by the HGNC.
Neurexophilin 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
NXPH1
Synonyms (NCBI Gene) Gene synonyms aliases
NPH1, Nbla00697
Chromosome Chromosome number
7
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
7p21.3
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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 information of associated ontologies with gene provided by GO database.
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 ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
604639 20693 ENSG00000122584
Protein
UniProt ID 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
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Breast cancer Breast Cancer in BRCA1 mutation carriers N/A N/A GWAS
Lung adenocarcinoma Lung adenocarcinoma (survival time) in never smokers N/A N/A GWAS
Neuroticism Neuroticism N/A N/A GWAS
Schizophrenia Schizophrenia N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Alzheimer Disease Associate 20100581
Autistic Disorder Associate 22016809
Diabetes Mellitus Associate 28068899
Nephronophthisis familial juvenile Associate 17601928
Neuroblastoma Associate 26646589
Obesity Associate 28068899
Pancreatic Intraductal Neoplasms Associate 22173550
Retinal Dysplasia Associate 22173550
Trigeminal Neuralgia Associate 38158702