Gene Information |
Gene ID: | | 8851 |
Symbol: | | CDK5R1 |
Full Name: | | cyclin-dependent kinase 5, regulatory subunit 1 (p35) |
Alias: | | CDK5P35|CDK5R|MGC33831|NCK5A|p23|p25|p35|p35nck5a |
Organism: | | Homo sapiens (Human) |
Chromosome: | | 17 |
Genetic Location: | | 17q11.2 |
Physical Location: | | 27838217-27842383 on NC_000017.9 |
Gene Type: | | protein-coding |
Orthologs: | | This gene has no orthologs in other dataset(s). |
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Gene in Ethanol Study Datasets |
Gene Information | Original ID1: | | AI003191 | Fold Change: | | 1.4, 1.4 | Note: | | Differential Expression on the cDNA array (two fold changes are from two case groups) |
| Dataset Information | Name: | | 11141048 | Method: | | Microarray | Tissue: | | Frontal cortex | Phenotype: | | Alcohol dependence (AD)/Alcohol abuse/Alcoholism | Publication: | | Lewohl et al. Alcohol Clin Exp Res. (2000) Gene expression in human alcoholism: microarray analysis of frontal cortex. PubMed | Summary: | | RNA was extracted from postmortem samples of superior frontal cortex of alcoholics and nonalcoholics. Relative levels of RNA were determined by array techniques. This study used both cDNA and oligonucleotide microarrays to provide coverage of a large number of genes and to allow cross-validation for those genes represented on both types of arrays. Expression levels were determined for over 4000 genes and 163 of these were found to differ by 40% or more between alcoholics and nonalcoholics. |
| Gene Information | Original ID1: | | X80343 | Fold Change: | | 2.52 | P Value: | | 0.0012 |
| Dataset Information | Name: | | 12774316 | Method: | | Microarray | Tissue: | | Temporal cortex | Phenotype: | | Alcohol dependence (AD)/Alcohol abuse/Alcoholism | Publication: | | Sokolov et al. J Neurosci Res. (2003) Transcription profiling reveals mitochondrial, ubiquitin and signaling systems abnormalities in postmortem brains from subjects with a history of alcohol abuse or dependence. PubMed | Summary: | | To identify candidate mechanisms for alcohol abuse, the expression of 12,626 genes was measured in postmortem temporal cortex from 11 subjects with a history of alcohol abuse or dependence, with or without other psychiatric diagnoses and compared pairwise with the expression in 11 nonalcoholic subjects matched for the other psychiatric diagnoses and demographics. Genes were defined to have altered expression in alcohol abuse if: 1) the gene showed decreased expression in at least 10 of 11 subjects with alcohol abuse, or showed increased expression in at least 10 of 11 subjects with this diagnosis compared to matched non-abusers (P<0.007, X2test); or 2) the difference in the mean abuser/non-abuser ratio for the gene from value of 1.0 was significant at P<0.05 (one sample t-test). In subjects with a history of alcohol abuse or dependence, 163 genes were changed significantly. |
| Gene Information | | Dataset Information | Name: | | 18477577 | Method: | | Addiction array gene list | Publication: | | Hodgkinson et al. Alcohol Alcohol. (2008) Addictions Biology: Haplotype-Based Analysis for 130 Candidate Genes on a Single Array. PubMed | Summary: | | To develop a panel of markers able to extract full haplotype information for candidate genes in alcoholism, other addictions and disorders of mood and anxiety. Methods: A total of 130 genes were haplotype tagged and genotyped in 7 case/control populations and 51 reference populations using Illumina GoldenGate SNP genotyping technology, determining haplotype coverage. The 130 candidate genes were selected on the basis of their roles in functional domains important in the addictions and in the related phenotypes of anxiety and depression. The candidate genes included a limited number involved in the pharmacokinetic domain (e.g. several genes in the ADH gene cluster, and ALDH genes). The majority of the genes represent the domains of vulnerability to drug use and pharmacodynamic response. These include dopamine, serotonin, glutamine, GABA, and opioid neurotransmitter genes, signaling genes, and genes modulating stress resiliency and behavioral dyscontrol domains. There is a high degree of overlap between functional gene categories because of pleiotropic actions of molecules on behavior. |
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Linkage Dataset | Marker | LOD | P value | Location (bp) | |
D17S798 | | | 28313925 | Region: | | 26313925-30313925 | Phenotype: | | Alcoholism phenotype along with age, gender, and P300 or constraint | Name: | | 15211641 | Method: | | Linkage | Publication: | | Hill et al. Am J Med Genet B Neuropsychiatr Genet. (2004) A genome wide search for alcoholism susceptibility genes. PubMed | Summary: | | A total of 360 markers for 22 autosomes were spaced at an average distance of 9.4cMand genotyping performed for 330 members of these multiplex families. Extensive clinical data, personality variation, and event-related potential characteristics were available for reducing heterogeneity and detecting robust linkage signals. Multipoint linkage analysis using different analytic strategies give strong support for loci on chromosomes 1, 2, 6, 7, 10, 12, 14, 16, and 17. Thirty five markers with LOD score >2.0 at baseline using the binary alcoholism phenotype along with age, gender, and P300 or constraint (Table III). Here we listed the genes between two near markers or genes near a separate marker (within 2Mb). |
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Gene Refseq Sequence Annotation |
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Gene Ontology (GO) Annotation |
GO ID | GO Term | Category | Evidence (PubMed) | |
GO:0030426 | growth cone | Cellular Component | ISS | |
GO:0030424 | axon | Cellular Component | ISS | |
GO:0016533 | cyclin-dependent protein kinase 5 activator complex | Cellular Component | IEA | |
GO:0016020 | membrane | Cellular Component | ISS | |
GO:0031594 | neuromuscular junction | Cellular Component | ISS | |
GO:0043025 | cell soma | Cellular Component | ISS | |
GO:0043197 | dendritic spine | Cellular Component | ISS | |
GO:0043292 | contractile fiber | Cellular Component | ISS | |
GO:0005737 | cytoplasm | Cellular Component | ISS | |
GO:0005634 | nucleus | Cellular Component | ISS | |
GO:0043539 | protein serine/threonine kinase activator activity | Molecular Function | ISS | |
GO:0045296 | cadherin binding | Molecular Function | ISS | |
GO:0016534 | cyclin-dependent protein kinase 5 activator activity | Molecular Function | IEA | |
GO:0004672 | protein kinase activity | Molecular Function | TAS (7592934) | |
GO:0005509 | calcium ion binding | Molecular Function | ISS | |
GO:0005515 | protein binding | Molecular Function | IPI (10721722|12223541) | |
GO:0005515 | protein binding | Molecular Function | ISS | |
GO:0031175 | neurite development | Biological Process | ISS | |
GO:0035235 | ionotropic glutamate receptor signaling pathway | Biological Process | ISS | |
GO:0043525 | positive regulation of neuron apoptosis | Biological Process | ISS | |
GO:0000079 | regulation of cyclin-dependent protein kinase activity | Biological Process | TAS (7592934) | |
GO:0009790 | embryonic development | Biological Process | ISS | |
GO:0001764 | neuron migration | Biological Process | ISS | |
GO:0007158 | neuron adhesion | Biological Process | ISS | |
GO:0007213 | acetylcholine receptor signaling, muscarinic pathway | Biological Process | ISS | |
GO:0007411 | axon guidance | Biological Process | ISS | |
GO:0007413 | axonal fasciculation | Biological Process | ISS | |
GO:0007420 | brain development | Biological Process | ISS | |
GO:0007420 | brain development | Biological Process | NAS (10915792) | |
GO:0008283 | cell proliferation | Biological Process | TAS (8090221) | |
GO:0045664 | regulation of neuron differentiation | Biological Process | NAS (10721722) | |
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Other Database Cross Links |
NCBI Entrez Gene: | | 8851 |
HGNC: | | 1775 |
Ensembl: | | ENSG00000176749 |
MIM: | | 603460 |
HPRD: | | 04586 |
HuGE Navigator: | | 8851 |
dbSNP: | | CDK5R1 |
GeneCard: | | CDK5R1 |
AceView: | | CDK5R1 |