Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
50863
Gene name Gene Name - the full gene name approved by the HGNC.
Neurotrimin
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
NTM
Synonyms (NCBI Gene) Gene synonyms aliases
CEPU-1, HNT, IGLON2, NTRI
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q25
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the IgLON (LAMP, OBCAM, Ntm) family of immunoglobulin (Ig) domain-containing glycosylphosphatidylinositol (GPI)-anchored cell adhesion molecules. The encoded protein may promote neurite outgrowth and adhesion via a homophilic
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT006824 hsa-miR-182-5p Luciferase reporter assay, Western blot 22917588
MIRT006824 hsa-miR-182-5p Luciferase reporter assay, Western blot 22917588
MIRT645476 hsa-miR-362-5p HITS-CLIP 23824327
MIRT645475 hsa-miR-500b-5p HITS-CLIP 23824327
MIRT645474 hsa-miR-501-5p 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:0005515 Function Protein binding IPI 21982860, 25416956, 31515488, 32296183
GO:0005576 Component Extracellular region TAS
GO:0005886 Component Plasma membrane IEA
GO:0005886 Component Plasma membrane TAS
GO:0007155 Process Cell adhesion IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
607938 17941 ENSG00000182667
Protein
UniProt ID Q9P121
Protein name Neurotrimin (hNT) (IgLON family member 2)
Protein function Neural cell adhesion molecule.
PDB 6DLF
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07679 I-set 36 132 Immunoglobulin I-set domain Domain
PF13927 Ig_3 135 205 Domain
PF13927 Ig_3 222 299 Domain
Sequence
Sequence length 344
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
Astrocytoma Astrocytoma, Pilocytic astrocytoma N/A N/A GWAS
Colorectal Cancer Colorectal cancer N/A N/A GWAS
Connective Tissue Disease Connective tissue disorder N/A N/A ClinVar
Dementia Dementia N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Aortic Aneurysm Thoracic Associate 23054244
Attention Deficit Disorder with Hyperactivity Associate 27021288
Autism Spectrum Disorder Associate 32807774
Carcinogenesis Associate 23495067
Carcinoma Ovarian Epithelial Associate 16115914
Colorectal Neoplasms Associate 35991839
Congenital disorder of glycosylation type 1A Associate 23054244
Developmental Disabilities Associate 23495067
Glaucoma Open Angle Associate 22661486
Idiopathic Pulmonary Fibrosis Associate 30720061