Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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50863 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Neurotrimin |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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NTM |
SynonymsGene synonyms aliases
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CEPU-1, HNT, IGLON2, NTRI |
ChromosomeChromosome number
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11 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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11q25 |
SummarySummary 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 |
miRNAmiRNA 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 IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
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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 |
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Domain |
PF13927 |
Ig_3 |
222 → 299 |
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Domain |
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Sequence |
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Sequence length |
344 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
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Associated diseases
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Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Attention deficit hyperactivity disorder |
Attention deficit hyperactivity disorder |
rs120074176, rs786205019 |
27021288 |
Leukemia |
Leukemia, Myelocytic, Acute |
rs121909646, rs121913488, rs587776834, rs752746786, rs869312821, rs767454740, rs1554564297, rs11978267, rs4132601 |
27903959 |
Myopia |
Myopia |
rs387907109, rs146936371, rs587776903, rs786205127, rs398122836, rs199624584, rs587777625, rs786205216, rs758872875, rs764211125, rs1135402746, rs765658563, rs1555941129, rs1555941116, rs199923805, rs782555528, rs1554862601, rs1586620121, rs1387950081, rs2051026773, rs1422332023 |
27182965 |
Schizophrenia |
Schizophrenia |
rs74315508, rs74315509, rs13447324, rs1558507406, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346, rs863223347, rs863223351, rs863223352, rs61734270, rs797045205, rs869312829, rs869312830, rs770913157, rs869312832, rs869312831, rs781720548, rs1262969313 |
21926974, 31374203 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Mental depression |
Unipolar Depression, Major Depressive Disorder |
rs587778876, rs587778877 |
21036197 |
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