Gene: TUBGCP5 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 114791
Gene Symbol: TUBGCP5
TUBGCP5 		0.010 GeneticVariation disease BEFREE Based on this evidence we suggest that the identified TUBGCP5 variant in our patient may thus represent a novel cause of MCPH with mild developmental delay and may play a role in occurrence of microcephaly in 15q11.2 microdeletion carriers. 30543990 2019