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
GO:0005576 Component Extracellular region TAS
GO:0005886 Component Plasma membrane TAS
GO:0007155 Process Cell adhesion IEA
GO:0008038 Process Neuron recognition TAS 7891157
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
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Attention deficit hyperactivity disorder Attention deficit hyperactivity disorder rs786205019 27021288
Leukemia Leukemia, Myelocytic, Acute rs121909646, rs121913488, rs587776834, rs752746786, rs869312821, rs767454740, rs1554564297 27903959
Myopia Myopia rs387907109, rs146936371, rs587776903, rs786205127, rs398122836, rs199624584, rs587777625, rs786205216, rs758872875, rs764211125, rs1135402746, rs765658563, rs1555941129, rs1555941116, rs199923805
View all (6 more)
27182965
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
21926974, 31374203
Unknown
Disease term Disease name Evidence References Source
Mental depression Unipolar Depression, Major Depressive Disorder 21036197 ClinVar
Metabolic Syndrome Metabolic Syndrome GWAS
Lung adenocarcinoma Lung adenocarcinoma Validation that loss of Tgfbr2 results in more aggressive and T cell-excluded KP lung tumors GWAS, CBGDA
Dementia Dementia GWAS
Associations from Text Mining
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