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Aliases for NTM Gene

Aliases for NTM Gene

  • Neurotrimin 2 2 3 3 5
  • IgLON Family Member 2 2 3 4
  • IGLON2 3 4
  • HNT 3 4
  • CEPU-1 3
  • NTRI 3
  • NT 4

External Ids for NTM Gene

Previous GeneCards Identifiers for NTM Gene

  • GC11P130746
  • GC11P131240
  • GC11P127736

Summaries for NTM Gene

Entrez Gene Summary for NTM 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 mechanism. This gene is closely linked to a related family member, opioid binding protein/cell adhesion molecule-like (OPCML), on chromosome 11. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2009]

GeneCards Summary for NTM Gene

NTM (Neurotrimin) is a Protein Coding gene. Diseases associated with NTM include Childhood Pilocytic Astrocytoma and Juvenile Pilocytic Astrocytoma. Among its related pathways are Metabolism of proteins and Post-translational modification- synthesis of GPI-anchored proteins. An important paralog of this gene is OPCML.

UniProtKB/Swiss-Prot for NTM Gene

  • Neural cell adhesion molecule.

Gene Wiki entry for NTM Gene

Additional gene information for NTM Gene

No data available for CIViC summary , Tocris Summary , PharmGKB "VIP" Summary , fRNAdb sequence ontologies and piRNA Summary for NTM Gene

Genomics for NTM Gene

Regulatory Elements for NTM Gene

Enhancers for NTM Gene
GeneHancer Identifier Enhancer Score Enhancer Sources Gene-Enhancer Score TSS distance (kb) Number of Genes Away Size (kb) Transcription Factor Binding Sites within enhancer Gene Targets for Enhancer
GH11H132050 1.3 FANTOM5 Ensembl ENCODE dbSUPER 11.6 +685.2 685179 10.2 JUND FOS NFE2 MAFK NTM ENSG00000224700 GC11P132142
GH11H132061 1.4 FANTOM5 Ensembl ENCODE dbSUPER 10.2 +695.0 695007 7.7 JUND CHD1 CREB1 FOS MAFK NTM GC11P132142 ENSG00000224700
GH11H132032 1 FANTOM5 ENCODE dbSUPER 8.2 +662.7 662718 1.5 PKNOX1 JUND POLR2A ENSG00000238117 NTM ENSG00000224700 GC11P132142
GH11H132070 1.4 FANTOM5 Ensembl ENCODE dbSUPER 5.8 +702.2 702151 4 ATF1 ZBTB21 JUN JUND POLR2A ZNF629 TARDBP CREB1 FOS NTM GC11P132142 ENSG00000224700
GH11H132125 1.2 FANTOM5 Ensembl ENCODE 6.4 +756.4 756371 2.9 CTCF POLR2A SUZ12 SMC3 CHD1 RAD21 NTM GC11P132142 ENSG00000224700
- Elite enhancer and/or Elite enhancer-gene association Download GeneHancer data dump

Enhancers around NTM on UCSC Golden Path with GeneCards custom track

Genomic Locations for NTM Gene

Genomic Locations for NTM Gene
966,462 bases
Plus strand

Genomic View for NTM Gene

Genes around NTM on UCSC Golden Path with GeneCards custom track

Cytogenetic band:
NTM Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
Genomic Location for NTM Gene
GeneLoc Logo Genomic Neighborhood Exon StructureGene Density

RefSeq DNA sequence for NTM Gene

Proteins for NTM Gene

  • Protein details for NTM Gene (UniProtKB/Swiss-Prot)

    Protein Symbol:
    Recommended name:
    Protein Accession:
    Secondary Accessions:
    • A0MTT2
    • Q6UXJ3
    • Q86VJ9

    Protein attributes for NTM Gene

    344 amino acids
    Molecular mass:
    37971 Da
    Quaternary structure:
    No Data Available

    Alternative splice isoforms for NTM Gene


neXtProt entry for NTM Gene

Post-translational modifications for NTM Gene

  • Glycosylation at posLast=4444, Asn70, posLast=152152, Asn284, posLast=292292, Asn305, and Asn321
  • Modification sites at PhosphoSitePlus

No data available for DME Specific Peptides for NTM Gene

Domains & Families for NTM Gene

Gene Families for NTM Gene

Human Protein Atlas (HPA):
  • Plasma proteins
  • Predicted intracellular proteins
  • Predicted membrane proteins
  • Predicted secreted proteins

Graphical View of Domain Structure for InterPro Entry



  • Belongs to the immunoglobulin superfamily. IgLON family.
  • Belongs to the immunoglobulin superfamily. IgLON family.
genes like me logo Genes that share domains with NTM: view

Function for NTM Gene

Molecular function for NTM Gene

UniProtKB/Swiss-Prot Function:
Neural cell adhesion molecule.

Phenotypes From GWAS Catalog for NTM Gene

Gene Ontology (GO) - Molecular Function for NTM Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0005515 protein binding IPI 21982860
genes like me logo Genes that share ontologies with NTM: view
genes like me logo Genes that share phenotypes with NTM: view

Clone Products

No data available for Enzyme Numbers (IUBMB) , Human Phenotype Ontology , Animal Models , Transcription Factor Targets and HOMER Transcription for NTM Gene

Localization for NTM Gene

Subcellular locations from UniProtKB/Swiss-Prot for NTM Gene

Cell membrane; Lipid-anchor, GPI-anchor.

Subcellular locations from

Extracellular space Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi Apparatus Nucleus Mitochondrion 0 1 2 3 4 5 Confidence
COMPARTMENTS Subcellular localization image for NTM gene
Compartment Confidence
plasma membrane 5
extracellular 4

Gene Ontology (GO) - Cellular Components for NTM Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0005576 extracellular region TAS --
GO:0005886 plasma membrane TAS --
GO:0016020 membrane IEA --
GO:0031225 anchored component of membrane IEA --
genes like me logo Genes that share ontologies with NTM: view

No data available for Subcellular locations from the Human Protein Atlas (HPA) for NTM Gene

Pathways & Interactions for NTM Gene

genes like me logo Genes that share pathways with NTM: view

Gene Ontology (GO) - Biological Process for NTM Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0006501 C-terminal protein lipidation TAS --
GO:0007155 cell adhesion NAS,IEA --
GO:0008038 neuron recognition TAS 7891157
genes like me logo Genes that share ontologies with NTM: view

No data available for SIGNOR curated interactions for NTM Gene

Drugs & Compounds for NTM Gene

(5) Drugs for NTM Gene - From: ClinicalTrials

Name Status Disease Links Group Role Mechanism of Action Clinical Trials
Clarithromycin Approved Pharma 299
Anti-Bacterial Agents Pharma 11831
Anti-Infective Agents Pharma 22631
Cytochrome P-450 CYP3A Inhibitors Pharma 1747
Cytochrome P-450 Enzyme Inhibitors Pharma 3990
genes like me logo Genes that share compounds with NTM: view

Transcripts for NTM Gene

Unigene Clusters for NTM Gene

Representative Sequences:

Clone Products

Alternative Splicing Database (ASD) splice patterns (SP) for NTM Gene

No ASD Table

Relevant External Links for NTM Gene

GeneLoc Exon Structure for
ECgene alternative splicing isoforms for

Expression for NTM Gene

mRNA expression in normal human tissues from GTEx, Illumina, BioGPS, and CGAP SAGE for NTM Gene

mRNA expression in embryonic tissues and stem cells from LifeMap Discovery

mRNA differential expression in normal tissues according to GTEx for NTM Gene

This gene is overexpressed in Brain - Cerebellar Hemisphere (x5.9), Brain - Cerebellum (x5.7), Brain - Cortex (x4.1), and Brain - Frontal Cortex (BA9) (x4.1).

Protein differential expression in normal tissues from HIPED for NTM Gene

This gene is overexpressed in Cerebrospinal fluid (27.6), Fetal Brain (16.5), Frontal cortex (9.6), and Retina (6.4).

Integrated Proteomics: protein expression in normal tissues and cell lines from ProteomicsDB, PaxDb, MaxQB, and MOPED for NTM Gene

Protein tissue co-expression partners for NTM Gene

- Elite partner

NURSA nuclear receptor signaling pathways regulating expression of NTM Gene:


SOURCE GeneReport for Unigene cluster for NTM Gene:


Evidence on tissue expression from TISSUES for NTM Gene

  • Skin(4)
genes like me logo Genes that share expression patterns with NTM: view

No data available for mRNA Expression by UniProt/SwissProt and Phenotype-based relationships between genes and organs from Gene ORGANizer for NTM Gene

Orthologs for NTM Gene

This gene was present in the common ancestor of animals.

Orthologs for NTM Gene

Organism Taxonomy Gene Similarity Type Details
(Pan troglodytes)
Mammalia NTM 33 34
  • 99.11 (n)
(Canis familiaris)
Mammalia NTM 33 34
  • 92.77 (n)
(Bos Taurus)
Mammalia NTM 33 34
  • 91.08 (n)
(Rattus norvegicus)
Mammalia Ntm 33
  • 90.99 (n)
(Ornithorhynchus anatinus)
Mammalia NTM 34
  • 89 (a)
(Mus musculus)
Mammalia Ntm 33 16 34
  • 87.69 (n)
(Monodelphis domestica)
Mammalia NTM 34
  • 79 (a)
(Gallus gallus)
Aves NTM 33 34
  • 78.93 (n)
(Anolis carolinensis)
Reptilia NTM 34
  • 83 (a)
tropical clawed frog
(Silurana tropicalis)
Amphibia ntm 33
  • 71.37 (n)
African clawed frog
(Xenopus laevis)
Amphibia Xl.26284 33
(Danio rerio)
Actinopterygii opcml 34
  • 60 (a)
fruit fly
(Drosophila melanogaster)
Insecta CG31708 33 34
  • 47.86 (n)
CG11320 34
  • 24 (a)
CG40378 34
  • 24 (a)
Ama 34
  • 23 (a)
CG14521 34
  • 23 (a)
CG14010 34
  • 22 (a)
CG42368 34
  • 22 (a)
Lac 34
  • 21 (a)
CG34391 34
  • 20 (a)
CG42343 34
  • 18 (a)
CG31646 34
  • 17 (a)
CG32791 34
  • 17 (a)
CG7166 34
  • 17 (a)
CG31814 34
  • 16 (a)
CG34353 34
  • 16 (a)
klg 34
  • 16 (a)
wrapper 34
  • 15 (a)
African malaria mosquito
(Anopheles gambiae)
Insecta AgaP_AGAP009965 33
  • 44.66 (n)
(Caenorhabditis elegans)
Secernentea rig-5 34
  • 19 (a)
sea squirt
(Ciona savignyi)
Ascidiacea -- 34
  • 29 (a)
Species where no ortholog for NTM was found in the sources mined by GeneCards:
  • A. gosspyii yeast (Ashbya gossypii)
  • Actinobacteria (Mycobacterium tuberculosis)
  • Alicante grape (Vitis vinifera)
  • alpha proteobacteria (Wolbachia pipientis)
  • amoeba (Dictyostelium discoideum)
  • Archea (Pyrococcus horikoshii)
  • baker's yeast (Saccharomyces cerevisiae)
  • barley (Hordeum vulgare)
  • beta proteobacteria (Neisseria meningitidis)
  • bread mold (Neurospora crassa)
  • Chromalveolata (Phytophthora infestans)
  • common water flea (Daphnia pulex)
  • corn (Zea mays)
  • E. coli (Escherichia coli)
  • filamentous fungi (Aspergillus nidulans)
  • Firmicute bacteria (Streptococcus pneumoniae)
  • fission yeast (Schizosaccharomyces pombe)
  • green algae (Chlamydomonas reinhardtii)
  • honey bee (Apis mellifera)
  • K. lactis yeast (Kluyveromyces lactis)
  • loblloly pine (Pinus taeda)
  • malaria parasite (Plasmodium falciparum)
  • medicago trunc (Medicago Truncatula)
  • moss (Physcomitrella patens)
  • orangutan (Pongo pygmaeus)
  • pig (Sus scrofa)
  • rainbow trout (Oncorhynchus mykiss)
  • rice (Oryza sativa)
  • rice blast fungus (Magnaporthe grisea)
  • schistosome parasite (Schistosoma mansoni)
  • sea anemone (Nematostella vectensis)
  • sea urchin (Strongylocentrotus purpuratus)
  • sorghum (Sorghum bicolor)
  • soybean (Glycine max)
  • stem rust fungus (Puccinia graminis)
  • sugarcane (Saccharum officinarum)
  • thale cress (Arabidopsis thaliana)
  • tomato (Lycopersicon esculentum)
  • toxoplasmosis (Toxoplasma gondii)
  • Trichoplax (Trichoplax adhaerens)
  • wheat (Triticum aestivum)

Evolution for NTM Gene

Gene Tree for NTM (if available)
Gene Tree for NTM (if available)

Paralogs for NTM Gene

Paralogs for NTM Gene

(6) SIMAP similar genes for NTM Gene using alignment to 7 proteins:

genes like me logo Genes that share paralogs with NTM: view

Variants for NTM Gene

Sequence variations from dbSNP and Humsavar for NTM Gene

SNP ID Clin Chr 11 pos Sequence Context AA Info Type
rs1000000568 -- 131,492,760(+) TTTGA(A/G)TACCA intron-variant
rs1000003942 -- 131,632,741(+) GCGAT(A/C)TCCAC intron-variant
rs1000005052 -- 131,723,858(+) AGAGA(C/G)AGACA intron-variant
rs1000008342 -- 132,046,809(+) ATCTG(C/T)CTGTC intron-variant
rs1000012034 -- 131,452,438(+) GATGG(C/T)TACTT intron-variant

Structural Variations from Database of Genomic Variants (DGV) for NTM Gene

Variant ID Type Subtype PubMed ID
nsv983214 CNV duplication 23825009
nsv952762 CNV deletion 24416366
nsv832296 CNV gain 17160897
nsv826135 CNV loss 20364138
nsv821528 CNV deletion 20802225
nsv556588 CNV loss 21841781
nsv556587 CNV loss 21841781
nsv556581 CNV gain 21841781
nsv556579 CNV gain 21841781
nsv556577 CNV gain+loss 21841781
nsv556 CNV deletion 18451855
nsv554 CNV insertion 18451855
nsv553 CNV insertion 18451855
nsv526844 CNV gain 19592680
nsv522510 CNV loss 19592680
nsv519866 CNV loss 19592680
nsv517550 CNV gain+loss 19592680
nsv513747 CNV insertion 21212237
nsv512244 CNV loss 21212237
nsv510281 OTHER sequence alteration 20534489
nsv499166 CNV gain 21111241
nsv474443 CNV novel sequence insertion 20440878
nsv468898 CNV gain 19166990
nsv428267 CNV loss 18775914
nsv428266 CNV gain 18775914
nsv39518 CNV insertion 16902084
nsv1151074 CNV duplication 26484159
nsv1143554 CNV deletion 24896259
nsv1141205 CNV duplication 24896259
nsv1129528 CNV tandem duplication 24896259
nsv1127239 CNV deletion 24896259
nsv1122683 CNV deletion 24896259
nsv1122682 CNV deletion 24896259
nsv1122681 CNV deletion 24896259
nsv1116687 CNV tandem duplication 24896259
nsv1116686 CNV tandem duplication 24896259
nsv1116685 CNV tandem duplication 24896259
nsv1113449 CNV deletion 24896259
nsv1113448 CNV deletion 24896259
nsv1070996 CNV deletion 25765185
nsv1053895 CNV gain 25217958
nsv1050988 CNV gain 25217958
nsv1044874 CNV gain 25217958
nsv1039087 CNV gain 25217958
nsv1036099 CNV loss 25217958
nsv1035733 CNV gain 25217958
esv993815 CNV deletion 20482838
esv9451 CNV gain 19470904
esv8607 CNV loss 19470904
esv3892111 CNV loss 25118596
esv3892110 CNV gain 25118596
esv3892109 CNV loss 25118596
esv3628122 CNV loss 21293372
esv3628121 CNV gain 21293372
esv3628120 CNV loss 21293372
esv3628119 CNV loss 21293372
esv3628115 CNV loss 21293372
esv3628113 CNV loss 21293372
esv3628112 CNV loss 21293372
esv3628111 CNV loss 21293372
esv3628109 CNV loss 21293372
esv3628108 CNV loss 21293372
esv3579979 CNV loss 25503493
esv3579974 CNV loss 25503493
esv3548540 CNV deletion 23714750
esv3548537 CNV deletion 23714750
esv3548533 CNV deletion 23714750
esv3408741 CNV duplication 20981092
esv3407733 CNV insertion 20981092
esv3406245 CNV insertion 20981092
esv3389636 CNV duplication 20981092
esv3369393 CNV duplication 20981092
esv3356717 CNV insertion 20981092
esv3337538 CNV insertion 20981092
esv3332815 CNV duplication 20981092
esv3304824 CNV mobile element insertion 20981092
esv3254718 CNV deletion 24192839
esv27663 CNV gain 19812545
esv2760178 CNV loss 21179565
esv2759873 CNV gain 17122850
esv275372 CNV gain+loss 21479260
esv2745284 CNV deletion 23290073
esv2745283 CNV deletion 23290073
esv2745282 CNV deletion 23290073
esv2745281 CNV deletion 23290073
esv2745280 CNV deletion 23290073
esv2745279 CNV deletion 23290073
esv2745278 CNV deletion 23290073
esv2745277 CNV deletion 23290073
esv2745276 CNV deletion 23290073
esv2745274 CNV deletion 23290073
esv2745273 CNV deletion 23290073
esv2745272 CNV deletion 23290073
esv2745271 CNV deletion 23290073
esv2745270 CNV deletion 23290073
esv2745269 CNV deletion 23290073
esv2745268 CNV deletion 23290073
esv2677132 CNV deletion 23128226
esv2675610 CNV deletion 23128226
esv2674917 CNV deletion 23128226
esv2672347 CNV deletion 23128226
esv2668524 CNV deletion 23128226
esv2666803 CNV deletion 23128226
esv2659747 CNV deletion 23128226
esv2652259 CNV deletion 19546169
esv26341 CNV loss 19812545
esv2632966 CNV deletion 19546169
esv25603 CNV loss 19812545
esv2517835 CNV insertion 19546169
esv24689 CNV gain 19812545
esv21641 CNV loss 19812545
esv2141370 CNV deletion 18987734
esv1929334 CNV deletion 18987734
esv1673449 CNV insertion 17803354
esv1589319 CNV insertion 17803354
esv1515834 CNV deletion 17803354
esv1453063 CNV deletion 17803354
esv1243815 CNV insertion 17803354
esv1186595 CNV deletion 17803354
esv1144589 CNV insertion 17803354
esv1008024 CNV deletion 20482838
esv1006260 CNV insertion 20482838
dgv739n106 CNV deletion 24896259
dgv738n106 CNV deletion 24896259
dgv424e212 CNV loss 25503493
dgv252n67 CNV gain 20364138
dgv236e214 CNV gain 21293372
dgv2202n54 CNV gain 21841781
dgv2201n54 CNV gain 21841781
dgv2200n54 CNV gain 21841781
dgv1299n100 CNV gain 25217958
dgv1298n100 CNV gain 25217958
dgv1297n100 CNV gain 25217958

Variation tolerance for NTM Gene

Residual Variation Intolerance Score: 22.3% of all genes are more intolerant (likely to be disease-causing)
Gene Damage Index Score: 1.94; 36.01% of all genes are more intolerant (likely to be disease-causing)

Relevant External Links for NTM Gene

Human Gene Mutation Database (HGMD)
SNPedia medical, phenotypic, and genealogical associations of SNPs for

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot for NTM Gene

Disorders for NTM Gene

MalaCards: The human disease database

(2) MalaCards diseases for NTM Gene - From: HGMD and DISEASES

Disorder Aliases PubMed IDs
childhood pilocytic astrocytoma
  • pediatric pilocytic astrocytoma
juvenile pilocytic astrocytoma
- elite association - COSMIC cancer census association via MalaCards
Search NTM in MalaCards View complete list of genes associated with diseases

Relevant External Links for NTM

Genetic Association Database (GAD)
Human Genome Epidemiology (HuGE) Navigator
Atlas of Genetics and Cytogenetics in Oncology and Haematology:
genes like me logo Genes that share disorders with NTM: view

No data available for UniProtKB/Swiss-Prot and Genatlas for NTM Gene

Publications for NTM Gene

  1. Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. (PMID: 20379614) Rose JE … Uhl GR (Molecular medicine (Cambridge, Mass.) 2010) 3 45 60
  2. Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study. (PMID: 20628086) Bailey SD … DREAM investigators (Diabetes care 2010) 3 45 60
  3. A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. (PMID: 20889312) Wang KS … Aragam N (Schizophrenia research 2010) 3 45 60
  4. Variants in several genomic regions associated with asperger disorder. (PMID: 21182207) Salyakina D … Pericak-Vance MA (Autism research : official journal of the International Society for Autism Research 2010) 3 45 60
  5. Signal peptide prediction based on analysis of experimentally verified cleavage sites. (PMID: 15340161) Zhang Z … Henzel WJ (Protein science : a publication of the Protein Society 2004) 3 4 60

Products for NTM Gene

Sources for NTM Gene

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