D1 family
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DRD1 |
5q35⋅1 |
Involved in memory, emotion and cognition, the functions that are highly disturbed in schizophrenics |
Grandy et al 1990; Litt et al 1991; Nothen et al 1993a; Cichon et al 1994; Liu et al 1995; Kojima et al 1999
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No significant association with any of the polymorphisms |
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Several polymorphisms in 5′ and 3′ UTR of the gene (Grandy et al 1990; Litt et al 1991; Dollfus et al 1996; Kojima et al 1999) |
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DRD5 |
4p 15⋅3 |
DRD5 is neuron specific and is localized within the limbic regions of the brain |
Asherson et al 1998
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No significant association |
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Displays high affinity for dopamine |
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D2 family
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DRD2 |
11q 22-q23 |
Second most abundant dopamine receptor |
Gejman et al 1994; Nanko et al 1994; Asherson et al 1994; Nothen et al 1994; Sobell et al 1994
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No significant association |
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Higher density of DRD2 in schizophrenic brains (Sedvall and Farde 1995) |
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Ser311/Cys311 polymorphism reported (Arinami et al 1994). Cys311 variant more in schizophrenics |
Shaikh et al 1994
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Positive association |
DRD3 |
3q13⋅3 |
Expression of DRD3 is restricted to the limbic areas of the brain, site for emotion and cognition that is highly disturbed inschizophrenics |
Crocq et al 1992; Nimgaonkar et al 1993; Mant et al 1994
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Significant association |
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Selective loss of DRD3 mRNA in parietal and motor regions of postmortem schizophrenic brains (Schmauss et al 1993) |
Nothen et al 1993b; Jonsson et al 1993; Nanko et al 1993; Chen et al 1997a; Prasad et al 1999
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No association |
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A to G substitution polymorphism leading to creation of MscI site in exon 1 of DRD3 gene and increased homozygosity at either allele is associated with schizophrenia (Crocq et al 1992) |
Please see Jonsson et al (1999) for exhaustive reference |
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DRD4 |
11p15⋅5 |
Higher affinity than other dopamine receptors for atypical antipsychotic clozapine |
Sommer et al 1993
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No significant association |
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Polymorphic 48 base pair repeat in putative third cytoplasmicloop |
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