Gene Gene information from NCBI Gene database.
Entrez ID 51299
Gene name Neuritin 1
Gene symbol NRN1
Synonyms (NCBI Gene)
NRNdJ380B8.2
Chromosome 6
Chromosome location 6p25.1
Summary 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.
93
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 (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
17
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 identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
607409 17972 ENSG00000124785
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
7
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
CARDIAC EMBOLISM GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CARDIOEMBOLIC STROKE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CENTRAL NERVOUS SYSTEM CANCER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
GLIOBLASTOMA MULTIFORME GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Acute Kidney Injury Associate 33863396
★☆☆☆☆
Found in Text Mining only
Alzheimer Disease Associate 37024090
★☆☆☆☆
Found in Text Mining only
Bipolar Disorder Associate 26700405
★☆☆☆☆
Found in Text Mining only
Carcinoma Associate 37185612
★☆☆☆☆
Found in Text Mining only
Cognition Disorders Associate 38165375
★☆☆☆☆
Found in Text Mining only
Emphysema Associate 19723343
★☆☆☆☆
Found in Text Mining only
Hearing Loss Associate 34530960
★☆☆☆☆
Found in Text Mining only
Hearing Loss Noise Induced Associate 34530960
★☆☆☆☆
Found in Text Mining only
Hypoxia Stimulate 16723126
★☆☆☆☆
Found in Text Mining only
Hypoxia Brain Associate 16723126
★☆☆☆☆
Found in Text Mining only