| Gene: Foxp1 (forkhead box P1) Chinchilla lanigera |
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Analyze |
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| Symbol: |
Foxp1 |
| Name: |
forkhead box P1 |
| Description: |
ENCODES a protein that exhibits androgen receptor binding (ortholog); core promoter sequence-specific DNA binding (ortholog); DNA-binding transcription factor activity (ortholog); INVOLVED IN cellular response to DNA damage stimulus (ortholog); chemokine (C-C motif) ligand 2 secretion (ortholog); endothelial cell activation (ortholog); ASSOCIATED WITH atrioventricular septal defect (ortholog); autism spectrum disorder (ortholog); autistic disorder (ortholog); FOUND IN nuclear chromatin (ortholog); nucleoplasm (ortholog); nucleus (ortholog) |
| Type: |
protein-coding
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| RefSeq Status: |
MODEL |
| Also known as: |
forkhead box protein P1 |
| Orthologs: |
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| Latest Assembly: |
ChiLan1.0 - Chinchilla ChiLan1.0 Assembly |
| Position: |
| Chinchilla Assembly | Chr | Position (strand) | Source | Genome Browsers |
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| JBrowse | NCBI | UCSC | Ensembl |
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ChiLan1.0 | NW_004955421 | 16,595,445 - 17,075,923 (+) | NCBI | ChiLan1.0 | ChiLan1.0 | | |
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| JBrowse: |
View Region in Genome Browser (JBrowse)
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| Model |
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 Disease Annotations
RGD Manual Annotations
| Barrett's esophagus | | ISS | RGD:11898748 | 9068941 | DNA:snp:enhancer:g.70879779A>C (rs2687201) (human) | RGD | PMID:25447851, REF_RGD_ID:11560527 | | Brain Injuries | treatment | ISS | RGD:11898748 | 9068941 | | RGD | PMID:26842647, REF_RGD_ID:11561903 | | complex cortical dysplasia with other brain malformations | | ISS | RGD:11898748 | 9068941 | protein:altered expression:neocortex (human) | RGD | PMID:22759905, REF_RGD_ID:11560525 | | congenital heart disease | | ISS | RGD:11898748 | 9068941 | DNA:missense mutation, deletion:cds, exons:p.P568S (human) | RGD | PMID:23766104, REF_RGD_ID:11071913 | | congestive heart failure | | ISS | RGD:11898748 | 9068941 | | RGD | PMID:16952980, REF_RGD_ID:1582564 | | esophagus adenocarcinoma | | ISS | RGD:11898748 | 9068941 | DNA:snps:intron, enhancer:g.70959438A>G, g.70879779A>C (rs9837992, rs2687201) (human) | RGD | PMID:26383589, REF_RGD_ID:11535321 | | Hemimegalencephaly | | ISS | RGD:11898748 | 9068941 | protein:altered expression:neocortex (human) | RGD | PMID:22759905, REF_RGD_ID:11560525 | | hepatocellular carcinoma | treatment | ISS | RGD:11898748 | 9068941 | | RGD | PMID:25156538, REF_RGD_ID:9587823 | | Huntington's disease | | ISS | RGD:11898748 | 9068941 | mRNA:decreased expression:striatum (mouse) | RGD | PMID:16405510, REF_RGD_ID:11560524 | | hypoplastic left heart syndrome | | ISS | RGD:11898748 | 9068941 | mRNA:decreased expression:interatrial septum (human) | RGD | PMID:18344372, REF_RGD_ID:11561899 | | lung adenocarcinoma | | ISS | RGD:11898748 | 9068941 | mRNA:decreased expression:lung (rat) | RGD | PMID:16023287, REF_RGD_ID:11561933 | | peritonitis | | ISS | RGD:11898748 | 9068941 | human gene in a mouse model | RGD | PMID:18799727, REF_RGD_ID:11561898 | | schizophrenia | | ISS | RGD:11898748 | 9068941 | DNA:snp:intron:g.71205600C>T (rsrs7372960) (human) | RGD | PMID:26460480, REF_RGD_ID:11353286 | | trichostrongyloidiasis | | ISS | RGD:11898748 | 9068941 | mRNA:increased expression:duodenum (rat) | RGD | PMID:21698235, REF_RGD_ID:11561920 | |
Imported Annotations - ClinVar
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| atrioventricular septal defect | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: AVC DEFECT | ClinVar | PMID:23766104, PMID:25741868 |
| autistic disorder | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: Autistic disorder of childhood onset | ClinVar | PMID:25741868 |
| autistic disorder | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: Autism | ClinVar | |
| Endocardial Cushion Defects | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: ENDOCARDIAL CUSHION DEFECT | ClinVar | PMID:23766104, PMID:25741868 |
| epilepsy | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: Seizures | ClinVar | PMID:25741868 |
| genetic disease | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:12692134 more ... |
| genetic disease | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:12692134 more ... |
| genetic disease | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: Inborn genetic diseases | ClinVar | PMID:12692134 more ... |
| hypoplastic left heart syndrome | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: Hypoplastic left heart syndrome | ClinVar | PMID:23766104, PMID:25741868 |
| Hypoplastic Left Heart Syndrome 1 | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: Hypoplastic left heart syndrome 1 | ClinVar | PMID:23766104, PMID:25741868 |
| intellectual disability | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: Mental-retardation | ClinVar | PMID:25741868 |
| intellectual disability-severe speech delay-mild dysmorphism syndrome | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: Mental retardation with language impairment and with or without autistic features | ClinVar | PMID:25741868, PMID:28708303 |
| intellectual disability-severe speech delay-mild dysmorphism syndrome | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: Intellectual Disability with Language Impairment and Autistic Features | ClinVar | PMID:20848658 more ... |
| intellectual disability-severe speech delay-mild dysmorphism syndrome | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: Intellectual Disability with Language Impairment and Autistic Features | ClinVar | |
| intellectual disability-severe speech delay-mild dysmorphism syndrome | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: Mental retardation with language impairment and with or without autistic features | ClinVar | PMID:24214399 |
| intellectual disability-severe speech delay-mild dysmorphism syndrome | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: Mental retardation with language impairment and with or without autistic features | ClinVar | PMID:12692134 more ... |
| intellectual disability-severe speech delay-mild dysmorphism syndrome | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: Mental retardation with language impairment and with or without autistic features | ClinVar | PMID:25326635, PMID:25741868 |
| intellectual disability-severe speech delay-mild dysmorphism syndrome | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: Intellectual Disability with Language Impairment and Autistic Features | ClinVar | PMID:23766104, PMID:25741868 |
| intellectual disability-severe speech delay-mild dysmorphism syndrome | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: Mental retardation with language impairment and with or without autistic features | ClinVar | PMID:20950788 |
| intellectual disability-severe speech delay-mild dysmorphism syndrome | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: Mental retardation with language impairment and with or without autistic features | ClinVar | PMID:26647308 |
| intellectual disability-severe speech delay-mild dysmorphism syndrome | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: Mental retardation with language impairment and with or without autistic features | ClinVar | PMID:23757202 |
| intellectual disability-severe speech delay-mild dysmorphism syndrome | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: Mental retardation with language impairment and with or without autistic features | ClinVar | PMID:12692134 more ... |
| intellectual disability-severe speech delay-mild dysmorphism syndrome | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: Mental retardation with language impairment and with or without autistic features | ClinVar | PMID:20950788, PMID:26647308 |
| intellectual disability-severe speech delay-mild dysmorphism syndrome | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: Mental retardation with language impairment and with or without autistic features | ClinVar | PMID:25131622, PMID:26647308 |
| intellectual disability-severe speech delay-mild dysmorphism syndrome | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: Intellectual Disability with Language Impairment and Autistic Features | ClinVar | PMID:18414213 more ... |
| intellectual disability-severe speech delay-mild dysmorphism syndrome | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: Mental retardation with language impairment and with or without autistic features | ClinVar | PMID:25741868 |
| Language Development Disorders | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: Speech delay | ClinVar | PMID:25741868 |
| Pulmonary Atresia with Ventricular Septal Defect | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: Pulmonary atresia with ventricular septal defect | ClinVar | PMID:23766104, PMID:25741868 |
| strabismus | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: Squint | ClinVar | PMID:25741868 |
| visceral heterotaxy | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: Heterotaxia | ClinVar | PMID:23766104, PMID:25741868 |
| visual epilepsy | | ISS | RGD:11898748 | 9068941 | ClinVar Annotator: match by term: Seizures | ClinVar | PMID:25741868 |
