{{Rsnum
|rsid=2452600
|Gene=PDLIM5
|Chromosome=4
|position=94575731
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|GMAF=0.2755
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=PDLIM5
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 47.3 | 42.9 | 9.8
| HCB | 35.3 | 46.3 | 18.4
| JPT | 30.1 | 46.9 | 23.0
| YRI | 81.4 | 17.2 | 1.4
| ASW | 70.2 | 26.3 | 3.5
| CHB | 35.3 | 46.3 | 18.4
| CHD | 44.0 | 45.9 | 10.1
| GIH | 79.0 | 18.0 | 3.0
| LWK | 88.1 | 11.9 | 0.0
| MEX | 58.2 | 36.4 | 5.5
| MKK | 69.9 | 24.4 | 5.8
| TSI | 44.1 | 47.1 | 8.8
| HapMapRevision=28
}}{{Venter SNP
|rsid=2452600
|allele=T
|frequency=0.25
|uid=1103654486690
|type=heterozygous_SNP
|hugo=PDLIM5
|ensembl gene=ENSG00000163110
|ensembl transcript=ENST00000317968
|sift=AFFECT FUNCTION
|disease=May play a role in genetic susceptibility to schizophrenia. PDLIM5 is commonly increased in the brain of patients with bipolar disorder, schizophrenia, and major depression.
}}

{{PMID Auto
|PMID=18197271
|Title=A major single nucleotide polymorphism of the PDLIM5 gene associated with recurrent major depressive disorder.
|OA=1
}}

{{PMID Auto
|PMID=19139070
|Title=Genome-wide analysis to predict protein sequence variations that change phosphorylation sites or their corresponding kinases.
|OA=1
}}

{{GET Evidence
|gene=PDLIM5
|aa_change=Ser136Phe
|aa_change_short=S136F
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2452600
|overall_frequency_n=2682
|overall_frequency_d=10758
|overall_frequency=0.249303
|n_genomes=18
|n_genomes_annotated=0
|n_haplomes=20
|n_articles=0
|n_articles_annotated=0
|nblosum100=5
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}