NTM (neurotrimin)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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50863 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Neurotrimin |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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NTM |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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CEPU-1, HNT, IGLON2, NTRI |
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Chromosome
Chromosome number
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11 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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11q25 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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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 |
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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| Protein | |||||||||||||||||||||
| UniProt ID | Q9P121 | ||||||||||||||||||||
| Protein name | Neurotrimin (hNT) (IgLON family member 2) | ||||||||||||||||||||
| Protein function | Neural cell adhesion molecule. | ||||||||||||||||||||
| PDB | 6DLF | ||||||||||||||||||||
| Family and domains |
Pfam
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| Sequence |
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| Sequence length | 344 | ||||||||||||||||||||
| Interactions | View interactions | ||||||||||||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
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