All individuals with variants in gene PBX1

8 entries on 1 page. Showing entries 1 - 8.
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AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

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Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00217302 - - - rF - - - - - - - SRXY - 1 1 Kenneth Mcelreavey
00316100 K136 PubMed: Heidet 2017 affected patient and 1st degree relative - - France - - - - - CAKUT renal dysplasia; unilateral kidney agenesis; dysmorphic features, intellectual disability, microcephaly 1 2 Johan den Dunnen
00316122 K175 PubMed: Heidet 2017 2-generation family, 1 affected, unaffected non-carrier parents F - France - - - - - CAKUT renal hypoplasia; deafness, scoliosis 1 1 Johan den Dunnen
00316124 K179 PubMed: Heidet 2017 2-generation family, 1 affected, unaffected non-carrier parents F - France - - - - - CAKUT renal hypoplasia; renal dysplasia; cysts; dysmorphic features, intellectual disability 1 1 Johan den Dunnen
00316126 K181 PubMed: Heidet 2017 2-generation family, 1 affected, unaffected non-carrier parents M - France - - - - - CAKUT renal hypoplasia; renal dysplasia; renal ectopy; deafness 1 1 Johan den Dunnen
00316131 K186 PubMed: Heidet 2017 2-generation family, affected fetus, unaffected non-carrier parents - - France - - - - - CAKUT renal hypoplasia 1 1 Johan den Dunnen
00433666 - - - - - - - - - - - CAKUTHED intellectual disability, autism, outer ear abnormality 1 1 Marketa Wayhelova
00451676 - - - F - - (not applicable) white - - - - ? HP:0000256, HP:0001510, HP:0031878, HP:0011913, HP:0002857, HP:0001763, HP:0000357, HP:0000358, HP:0000377, HP:0000664, HP:0000490, HP:0006483, HP:0001800, HP:0011342, HP:0002015, HP:0008915, HP:0000750, HP:0000545, HP:0000483 1 1 Marketa Wayhelova
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