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 21873635
GO:0005576 Component Extracellular region 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
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Narcolepsy Narcolepsy rs104894574, rs387906655 19629137
Unknown
Disease term Disease name Evidence References Source
Schizophrenia Schizophrenia GWAS
Breast cancer Breast cancer Importantly, breast cancer patients bearing PRC2 LOF mutations displayed significantly worse prognosis compared with PRC2 wild-type patients GWAS, CBGDA
Neuroticism Neuroticism GWAS
Lung adenocarcinoma Lung adenocarcinoma Validation that loss of Tgfbr2 results in more aggressive and T cell-excluded KP lung tumors GWAS, CBGDA
Associations from Text Mining
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