Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
51299
Gene name Gene Name - the full gene name approved by the HGNC.
Neuritin 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
NRN1
Synonyms (NCBI Gene) Gene synonyms aliases
NRN, dJ380B8.2
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6p25.1
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the neuritin family, and is expressed in postmitotic-differentiating neurons of the developmental nervous system and neuronal structures associated with plasticity in the adult. The expression of this gene can be induced by n
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT028913 hsa-miR-26b-5p Microarray 19088304
MIRT050310 hsa-miR-25-3p CLASH 23622248
MIRT049996 hsa-miR-28-5p CLASH 23622248
MIRT626909 hsa-miR-7110-3p HITS-CLIP 23824327
MIRT626908 hsa-miR-6817-3p HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005576 Component Extracellular region TAS
GO:0005615 Component Extracellular space IEA
GO:0005886 Component Plasma membrane IBA
GO:0005886 Component Plasma membrane IEA
GO:0005886 Component Plasma membrane TAS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
607409 17972 ENSG00000124785
Protein
UniProt ID Q9NPD7
Protein name Neuritin
Protein function Promotes neurite outgrowth and especially branching of neuritic processes in primary hippocampal and cortical cells.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15056 NRN1 31 117 Neuritin protein family Domain
Sequence
Sequence length 142
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Post-translational modification: synthesis of GPI-anchored proteins
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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
Glioblastoma Glioblastoma N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Acute Kidney Injury Associate 33863396
Alzheimer Disease Associate 37024090
Bipolar Disorder Associate 26700405
Carcinoma Associate 37185612
Cognition Disorders Associate 38165375
Emphysema Associate 19723343
Hearing Loss Associate 34530960
Hearing Loss Noise Induced Associate 34530960
Hypoxia Stimulate 16723126
Hypoxia Brain Associate 16723126