Gene Gene information from NCBI Gene database.
Entrez ID 50863
Gene name Neurotrimin
Gene symbol NTM
Synonyms (NCBI Gene)
CEPU-1HNTIGLON2NTRI
Chromosome 11
Chromosome location 11q25
Summary 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.
95
miRTarBase ID miRNA Experiments Reference
MIRT006824 hsa-miR-182-5p Luciferase reporter assayWestern blot 22917588
MIRT006824 hsa-miR-182-5p Luciferase reporter assayWestern 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 (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
10
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 identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
607938 17941 ENSG00000182667
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
3
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Connective tissue disorder Likely benign rs375999981, rs201653643, rs139579932 RCV000680599
RCV000680600
RCV000680601
Associations from Text MiningDisease 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