| Primary information |
|---|
| Humcfs Id | Humcfs_3157 |
| chromosome_number | chromosome11 |
| name | FRA11H |
| chrlocation | 63400001-77100000 |
| cytoband | 11q13 |
| type | Aphidicolin |
| frequency | Common |
| gene_ensembl_id | ENSG00000110076 |
| gene_name | NRXN2 |
| havana_transcript_id | OTTHUMT00000320927 |
| gene_location | 64668482-64713097 |
| gene_orientation | - |
| exon_id | ENSE00001593409, ENSE00003498235, ENSE00001120040, ENSE00003490413, ENSE00001638964 |
| exon_number | 5 |
| gene_description | neurexin 2 |
| disease_description | Language Delay,Child Development Disorders, Pervasive,Autism Spectrum Disorders,Intellectual Disability,Leukocyte Adhesion Deficiency, Type III,Autistic Disorder,Schizophrenia,Malignant neoplasm of breast,Atrial Septal Defects |
| miRNA_location | NA |
| miRNA_strand | NA |
| miRNA_id | NA |
| miRNA_name | NA |
| miRNA_derived | NA |
| Technique | Karyotyping |
| PMID | 23852038 |
| Get Gene Informations in: | Gene Card, GEPIA, COSMIC, OMIM, EBI, HPA, DrugBank |