1. Gene
  2. Disc1 - DISC1 scaffold protein Gene

Disc1 - DISC1 scaffold protein Gene

Rattus norvegicus
Gene ID: 307940 | Gene type: protein coding

About Disc1

Summary

Enables Kinesin binding activity. Involved in several processes, including positive regulation of cell projection organization; protein localization to centrosome; and pyramidal neuron migration to cerebral cortex. Acts upstream of or within regulation of glutamatergic synaptic transmission. Located in several cellular components, including central region of growth cone; microtubule cytoskeleton; and perinuclear region of cytoplasm. Part of dynein complex and Kinesin complex. Human ortholog(s) of this gene implicated in autism spectrum disorder (multiple); bipolar disorder; chronic fatigue syndrome; major depressive disorder; and psychotic disorder (multiple). Orthologous to human DISC1 (DISC1 scaffold protein). [provided by Alliance of Genome Resources, Apr 2022]

Disc1 Products(1)

mRNA Protein Name
NM_175596.3 NP_783186.2 disrupted in schizophrenia 1 homolog
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables kinesin binding IDA
IDA: Inferred from direct assay
17202468 RGD
enables protein binding IPI
IPI: Inferred from physical interaction
17035248 RGD
enables protein-containing complex binding IDA
IDA: Inferred from direct assay
16299498 RGD
enables protein-containing complex binding IPI
IPI: Inferred from physical interaction
17202468 RGD
Biological Process GO Annotation Evidence Reference Source
involved in cilium assembly IMP
IMP: Inferred from mutant phenotype
20531939 RGD
involved in nervous system development IMP
IMP: Inferred from mutant phenotype
12506198 RGD
involved in positive regulation of axon extension IMP
IMP: Inferred from mutant phenotype
17202468 RGD
involved in positive regulation of cell-matrix adhesion IMP
IMP: Inferred from mutant phenotype
20479754 RGD
involved in positive regulation of neuron projection development IMP
IMP: Inferred from mutant phenotype
16299498 RGD
involved in protein localization to centrosome IGI
IGI: Inferred from genetic interaction
18762586 RGD
involved in protein localization to centrosome IMP
IMP: Inferred from mutant phenotype
18762586 RGD
involved in pyramidal neuron migration to cerebral cortex IMP
IMP: Inferred from mutant phenotype
16299498 RGD
involved in regulation of dendritic spine development IMP
IMP: Inferred from mutant phenotype
20139976 RGD
involved in regulation of neuron projection development IMP
IMP: Inferred from mutant phenotype
17035248 RGD
acts upstream of or within regulation of synaptic transmission, glutamatergic IMP
IMP: Inferred from mutant phenotype
24706880 RGD
involved in response to electrical stimulus IEP
IEP: Inferred from expression pattern
19499587 RGD
Cellular Component GO Annotation Evidence Reference Source
located in axon IDA
IDA: Inferred from direct assay
17202468 RGD
located in cell body IDA
IDA: Inferred from direct assay
17202468 RGD
located in central region of growth cone IDA
IDA: Inferred from direct assay
17202468 RGD
located in centrosome IDA
IDA: Inferred from direct assay
16299498 RGD
part of dynein complex IDA
IDA: Inferred from direct assay
16299498 RGD
part of kinesin complex IDA
IDA: Inferred from direct assay
17202468 RGD
located in microtubule IDA
IDA: Inferred from direct assay
17202468 RGD
located in perinuclear region of cytoplasm IDA
IDA: Inferred from direct assay
17418909 RGD
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

disrupted in schizophrenia 1 homolog

Orthologs Information

Species Symbol Source ID
Homo sapiens Disc1 NCBI NCBI:27185