Gene: TRAPPC9 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 83696
Gene Symbol: TRAPPC9
TRAPPC9 		0.050 GeneticVariation disease BEFREE Mutations in TRAPPC9 have been linked to a rare consanguineous hereditary form of mental retardation, as part of the NF‑κB pathways. 30272317 2018
Entrez Id: 83696
Gene Symbol: TRAPPC9
TRAPPC9 		0.050 GeneticVariation disease BEFREE TRAPPC9 gene mutations have been linked recently to autosomal recessive mental retardation 13 (MRT13; MIM#613192) with only eight families reported world-wide. 29031008 2017
Entrez Id: 83696
Gene Symbol: TRAPPC9
TRAPPC9 		0.050 GeneticVariation disease BEFREE Computational analysis of TRAPPC9: candidate gene for autosomal recessive non-syndromic mental retardation. 24040793 2014
Entrez Id: 83696
Gene Symbol: TRAPPC9
TRAPPC9 		0.050 GeneticVariation disease BEFREE Mutations in the TRAPP complex subunit 2 (TRAPPC2) cause X-linked spondyloepiphyseal dysplasia tarda, while mutations in the TRAPP complex subunit 9 (TRAPPC9) cause postnatal mental retardation with microcephaly. 21858081 2011
Entrez Id: 83696
Gene Symbol: TRAPPC9
TRAPPC9 		0.050 GeneticVariation disease BEFREE Identification of mutations in TRAPPC9, which encodes the NIK- and IKK-beta-binding protein, in nonsyndromic autosomal-recessive mental retardation. 20004765 2009