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Symbol Name ID |
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| Feature Type | protein coding gene | ||||||||||||||||||
| Genetic Map | |||||||||||||||||||
| Sequence Map |
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Vertebrate homology |
HomoloGene:10257 Vertebrate Homology Class 1 human; 1 mouse; 1 rat; 1 chimpanzee; 1 rhesus macaque; 1 cattle; 1 dog; 1 chicken Gene Tree: Disc1 |
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| Human homologs |
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Alleles and phenotypes |
All alleles(5) :
Targeted(2)
Spontaneous(1)
Chemically induced(2)
Homozygotes for a null allele show altered anxiety, synaptic depression, LTP, impulsivity, social investigation, hyperactivity and prepulse inhibition. Homozygotes for a spontaneous allele show altered working memory. Different ENU mutations cause distinct depression and schizophrenia-like profiles. Human Diseases Modeled Using Mouse Disc1 (2) Alleles Annotated to Human Diseases(3) |
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Gene Ontology (GO) classifications |
All GO classifications: (55 annotations)
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| Expression |
Literature Summary: (13 records) Data Summary: Results (144) Tissues (39) Images (38) Theiler Stages: 22, 23, 24, 25, 26, 28
External Resources: Allen Institute GEO ArrayExpress |
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Molecular reagents |
All nucleic(8)
Genomic(3)
cDNA(4)
Other(1)
Microarray probesets(1) |
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Other database links |
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| Sequences |
All sequences(51) RefSeq(5) UniProt(2) |
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| Polymorphisms | SNPs(659 from dbSNP Build 128) | ||||||||||||||||||
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Protein-related information |
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| References |
(Earliest) J:80804
Ma L, et al., Cloning and Characterization of Disc1, the Mouse Ortholog of DISC1 (Disrupted-in-Schizophrenia 1). Genomics. 2002 Dec;80(6):662-72 (Latest) J:195189 Ritchie D, et al., Disc1 deletion is present in Swiss-derived inbred mouse strains: implications for transgenic studies of learning and memory. Lab Anim. 2013 Apr 5; All references(65) |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/22/2013 MGI 5.13 |
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