chr7:113726546:> Detail (hg19)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr7:113,726,546-114,333,827 |
| hg38 | chr7:114,086,491-114,693,772 |
HGVS
| Type | Transcript | Protein |
|---|---|---|
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Frequency
[No Data.]
Prediction
[No Data.]
ClinVar
| Clinical Significance | |
| Review star | [No Data.] |
| Show details | |
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
| Score | Disease name | Description | Source | Pubmed | Links |
|---|---|---|---|---|---|
| <0.001 | child abuse behavior | NA | BeFree | Detail | |
| <0.001 | Cognition Disorders | NA | BeFree | Detail | |
| 0.001 | Communication impairment | NA | BeFree | Detail | |
| 0.120 | adenoid cystic carcinoma | NA | CTD_human | Detail | |
| <0.001 | Mental Depression | Striatal districts known to be differently related to these two modes of learnin... | BeFree | 25225386 | Detail |
| <0.001 | depressive disorder | Striatal districts known to be differently related to these two modes of learnin... | BeFree | 25225386 | Detail |
| <0.001 | Diabetes Mellitus, Non-Insulin-Dependent | NA | BeFree | Detail | |
| 0.001 | epilepsy | NA | BeFree | Detail | |
| <0.001 | Hallucinations | NA | BeFree | Detail | |
| <0.001 | Atrial Septal Defects | NA | BeFree | Detail | |
| <0.001 | Inflammatory Bowel Diseases | NA | BeFree | Detail | |
| 0.008 | Speech and language disorder | We show that TBR1 homodimerizes, that it interacts with FOXP2, a transcription f... | BeFree | 25232744 | Detail |
| 0.008 | Speech and language disorder | The first gene directly implicated in a speech and language disorder was FOXP2. | BeFree | 25597031 | Detail |
| 0.002 | Language Development Disorders | NA | GAD | Detail | |
| 0.017 | Language Disorders | NA | BeFree,LHGDN | Detail | |
| <0.001 | Adult T-Cell Lymphoma/Leukemia | NA | BeFree | Detail | |
| <0.001 | lymphoma | NA | BeFree | Detail | |
| <0.001 | microcephaly | NA | BeFree | Detail | |
| <0.001 | Monoclonal Gammopathy of Undetermined Significance | NA | BeFree | Detail | |
| <0.001 | Movement Disorders | NA | BeFree | Detail | |
| <0.001 | multiple myeloma | NA | BeFree | Detail | |
| <0.001 | Neoplasm Metastasis | MSC-regulated microRNAs converge on the transcription factor FOXP2 and promote b... | BeFree | 25515522 | Detail |
| <0.001 | nervous system disorder | NA | BeFree | Detail | |
| 0.002 | obesity | NA | GAD | Detail | |
| <0.001 | schizoaffective disorder | NA | BeFree | Detail | |
| 0.012 | schizophrenia | NA | BeFree,GAD,LHGDN | Detail | |
| 0.005 | Speech Disorders | NA | BeFree,LHGDN | Detail | |
| <0.001 | stuttering | NA | BeFree | Detail | |
| <0.001 | Unipolar Depression | NA | BeFree | Detail | |
| 0.120 | Russell-Silver syndrome | NA | BeFree,CTD_human | Detail | |
| 0.001 | Speech impairment | NA | BeFree | Detail | |
| <0.001 | Primary Progressive Aphasia (disorder) | NA | BeFree | Detail | |
| <0.001 | Phobic anxiety disorder | NA | BeFree | Detail | |
| 0.001 | Apraxia, Verbal | NA | BeFree | Detail | |
| <0.001 | Malignant neoplasm of prostate | NA | BeFree | Detail | |
| 0.120 | Craniofacial Abnormalities | NA | CTD_human | Detail | |
| 0.001 | specific language impairment | This, together with the different brain expression patterns of GNPTAB, GNPTG, an... | BeFree | 24807205 | Detail |
| <0.001 | dyslexia | NA | BeFree | Detail | |
| <0.001 | prostate carcinoma | NA | BeFree | Detail | |
| <0.001 | breast carcinoma | MSC-regulated microRNAs converge on the transcription factor FOXP2 and promote b... | BeFree | 25515522 | Detail |
| <0.001 | Emotional abuse | NA | BeFree | Detail | |
| 0.484 | Apraxia, Developmental Verbal | We studied the potential contribution to stuttering from variants in the FOXP2 g... | BeFree,CLINVAR,CTD_human,ORPHANET,UNIPROT | 24807205 | Detail |
| <0.001 | Communication Disorders, Developmental | NA | BeFree | Detail | |
| <0.001 | Frontotemporal Lobar Degeneration | NA | BeFree | Detail | |
| <0.001 | Stuttering, Developmental | A study of the role of the FOXP2 and CNTNAP2 genes in persistent developmental s... | BeFree | 24807205 | Detail |
| <0.001 | Reading Disabilities | NA | BeFree | Detail | |
| <0.001 | major depressive disorder | NA | BeFree | Detail | |
| 0.120 | Blood pressure finding | NA | GWASCAT | Detail | |
| 0.120 | Systemic arterial pressure | NA | GWASCAT | Detail | |
| <0.001 | Autism Spectrum Disorders | However, when the interaction term was omitted, neither MAOA nor FOXP2 was assoc... | BeFree | 24356376 | Detail |
| <0.001 | Neurodevelopmental Disorders | NA | BeFree | Detail | |
| <0.001 | Perisylvian syndrome | NA | BeFree | Detail | |
| <0.001 | GRN-related frontotemporal dementia | NA | BeFree | Detail | |
| 0.121 | Apraxias | NA | BeFree,CTD_human | Detail | |
| 0.002 | Articulation Disorders | NA | GAD | Detail | |
| 0.128 | autistic disorder | Interaction between MAOA and FOXP2 in association with autism and verbal communi... | BeFree,CTD_human,GAD | 24356376 | Detail |
| <0.001 | Mental disorders | NA | BeFree | Detail | |
| <0.001 | bipolar disorder | NA | BeFree | Detail | |
| <0.001 | Malignant neoplasm of breast | MSC-regulated microRNAs converge on the transcription factor FOXP2 and promote b... | BeFree | 25515522 | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| Striatal districts known to be differently related to these two modes of learning are affected diffe... | DisGeNET | Detail |
| Striatal districts known to be differently related to these two modes of learning are affected diffe... | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| We show that TBR1 homodimerizes, that it interacts with FOXP2, a transcription factor implicated in ... | DisGeNET | Detail |
| The first gene directly implicated in a speech and language disorder was FOXP2. | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| MSC-regulated microRNAs converge on the transcription factor FOXP2 and promote breast cancer metasta... | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| This, together with the different brain expression patterns of GNPTAB, GNPTG, and NAGPA compared to ... | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| MSC-regulated microRNAs converge on the transcription factor FOXP2 and promote breast cancer metasta... | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| We studied the potential contribution to stuttering from variants in the FOXP2 gene, which have prev... | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| A study of the role of the FOXP2 and CNTNAP2 genes in persistent developmental stuttering. | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| However, when the interaction term was omitted, neither MAOA nor FOXP2 was associated with autism sp... | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| Interaction between MAOA and FOXP2 in association with autism and verbal communication in a Korean p... | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| MSC-regulated microRNAs converge on the transcription factor FOXP2 and promote breast cancer metasta... | DisGeNET | Detail |
Overlapped Transcript Coordinates
| Gene | Transcript ID | Exon Number | Chromosome | Start | Stop | Type | Amino Mutation | Transcript Position | Links |
|---|
Overlapped Transcript
| Gene | Transcript ID | Chromosome | Start | Stop | Links |
|---|
- Gene
- -
- Genome
- hg19
- Position
- chr7:113,726,546-114,333,827
- Variant Type
- snv
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