Full data view for gene PEX6

This database is one of the dbPEX gene variant databases.
Information The variants shown are described using the NM_000287.3 transcript reference sequence.

14 entries on 1 page. Showing entries 1 - 14.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Allele     

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Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Re-site     

VIP     

Methylation     

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Technique     

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Disease     

ID_report     

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Owner     
+/. 10 c.1802G>A r.(?) p.(Arg601Gln) Parent #1 - pathogenic g.42935188C>T g.42967450C>T - - PEX6_000006 - PubMed: Ratbi 2015, Journal: Ratbi 2015 - - Germline yes - - - - DNA SEQ, SEQ-NG - - HMLR1 Fam6PatII1 PubMed: Ratbi 2015, Journal: Ratbi 2015 2-generation family, twin sisters, unaffected heterozygous carrier parents F no United Kingdom (Great Britain) - >21y - - - 2 Jamie Zeegers
+/. 10 c.1802G>A r.(?) p.(Arg601Gln) Parent #1 - pathogenic g.42935188C>T g.42967450C>T - - PEX6_000006 - PubMed: Ratbi 2015, Journal: Ratbi 2015 - - Germline yes - - - - DNA SEQ, SEQ-NG - - HMLR1 Fam6PatII2 PubMed: Ratbi 2015, Journal: Ratbi 2015 - F no United Kingdom (Great Britain) - >21y - - - 1 Jamie Zeegers
+/. 10 c.1802G>A r.(?) p.Arg601Gln Unknown - NA g.42935188C>T g.42967450C>T - - PEX6_000006 cDNA expression cloning in PEX6 defective fibroblasts showed reduced complementation (0.35) PubMed: Ratbi 2015, Journal: Ratbi 2015 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.1802G>A r.(?) p.(Arg601Gln) Unknown - pathogenic g.42935188C>T g.42967450C>T PEX6(NM_000287.3):c.1802G>A (p.R601Q), PEX6(NM_000287.4):c.1802G>A (p.R601Q) - PEX6_000006 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.1802G>A r.(?) p.(Arg601Gln) Unknown - pathogenic g.42935188C>T g.42967450C>T PEX6(NM_000287.3):c.1802G>A (p.R601Q), PEX6(NM_000287.4):c.1802G>A (p.R601Q) - PEX6_000006 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. 8 c.1802G>A r.(?) p.(Arg601Gln) Parent #1 - pathogenic (recessive) g.42935188C>T - - - PEX6_000006 - - - - Germline - - - - - DNA SEQ - - PBD - - - - - United States - - - - - 1 Nancy Braverman
+/. - c.1802G>A r.(?) p.(Arg601Gln) Parent #1 - pathogenic (recessive) g.42935188C>T - - - PEX6_000006 - PubMed: Yik 2009, MORL Deafness Variation Database - - Germline - - - - - DNA SEQ - - PBD Pat713 PubMed: Yik 2009 - - - United States - - - - - 1 Global Variome, with Curator vacancy
+/. - c.1802G>A r.(?) p.(Arg601Gln) Parent #1 - pathogenic (recessive) g.42935188C>T - - - PEX6_000006 - PubMed: Yik 2009, MORL Deafness Variation Database - - Germline - - - - - DNA SEQ - - PBD Pat609 PubMed: Yik 2009 - - - United States - - - - - 1 Global Variome, with Curator vacancy
+/. 8 c.1802G>A r.(?) p.(Arg601Gln) Parent #1 - pathogenic (recessive) g.42935188C>T g.42967450C>T - - PEX6_000006 - PubMed: Yik 2009 - - Germline - - - - - DNA SEQ - - PBD Pat704 PubMed: Yik 2009 - - - United States - - - - - 1 Johan den Dunnen
+/. - c.1802G>A r.(?) p.(Arg601Gln) Unknown - pathogenic (recessive) g.42935188C>T - - - PEX6_000006 - PubMed: Yik 2009 - - Germline - - - - - DNA SEQ - - PBD Pat672 PubMed: Yik 2009 - - - United States - - - - - 1 Johan den Dunnen
-/. - c.1802G>A r.(?) p.(Arg601Gln) Unknown - benign g.42935188C>T g.42967450C>T - - PEX6_000006 - PubMed: Yik 2009 - - Germline - 0.03 - - - DNA SEQ - - PBD - PubMed: Yik 2009 - - - United States - - - - - 1 Johan den Dunnen
+/. - c.1802G>A r.(?) p.(Arg601Gln) Paternal (confirmed) - pathogenic (recessive) g.42935188C>T - - - PEX6_000006 This variant was noted as heterozygous in this patient. The variant is previously associated with Heimler syndrome, a peroxisomal biogenesis disorder. Possible explanation for this patient, however a second variant in PEX6 is yet to be identified. Doucette 2021, submitted ClinVar-198709 rs34324426 Germline yes - - - - DNA SEQ-NG - - DFNB, maculopathy M73 II-1 Doucette 2021, submitted single child to unaffected parents (father was unavailable for examination) M yes Canada Middle Eastern - - Yes - 1 Lance P Doucette
+/. - c.1802G>A r.(?) p.(Arg601Gln) Unknown - pathogenic g.42935188C>T - PEX6(NM_000287.3):c.1802G>A (p.R601Q), PEX6(NM_000287.4):c.1802G>A (p.R601Q) - PEX6_000006 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. 8 c.1802G>A r.(1802g>a) p.(Arg601Gln) Parent #2 ACMG likely pathogenic g.42935188C>T g.42967450C>T - - PEX6_000006 - PubMed: Reurink 2023, Journal: Reurink 2023 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease USH11 PubMed: Reurink 2023, Journal: Reurink 2023 - - - - - - - - - 1 Janine Reurink
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