Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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50863
|
Gene name
Gene Name - the full gene name approved by the HGNC.
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Neurotrimin |
Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
|
NTM |
Synonyms (NCBI Gene)
Gene synonyms aliases
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CEPU-1, HNT, IGLON2, NTRI |
Chromosome
Chromosome number
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11 |
Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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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 |
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, rs782555528, rs1554862601, rs1586620121, rs1387950081, rs2051026773, rs1422332023 View all (6 more) |
27182965 |
Schizophrenia |
Schizophrenia |
rs13447324, 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 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 |
Prostate cancer |
Prostate cancer |
Together, these results show that PRRX2 is an oncogene and might play a role in the aggressiveness of PC within the DNPC population. |
|
GWAS, CBGDA |
Colorectal Cancer |
Colorectal Cancer |
In summary, our data strongly demonstrated that upregulation of GRB7 conferred MEKi resistance in CRC cells with KRAS mutations by mediating RTK signaling through the recruitment of PLK1. |
|
GWAS, CBGDA |
Astrocytoma |
Astrocytoma |
|
|
GWAS |
Insomnia |
Insomnia |
|
|
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 |
Intracranial Aneurysm |
Associate
|
23054244, 34668355 |
Leiomyoma |
Stimulate
|
32033718 |
Neoplasms |
Associate
|
16115914, 23495067 |
Osteogenesis imperfecta type 1A |
Associate
|
34668355 |
Ovarian Neoplasms |
Associate
|
16115914 |
Personality Disorders |
Associate
|
27021288 |
Prostatic Neoplasms |
Associate
|
33934205 |
Squamous Cell Carcinoma of Head and Neck |
Associate
|
28814981 |
|