Predicting the Most Deleterious Missense Nonsynonymous Single-Nucleotide Polymorphisms of Hennekam Syndrome-Causing CCBE1 Gene, In Silico Analysis

Table 1

Genes coexpressed and sharing a domain with CCBE1.

Gene symbol	Description	Coexpression	Shared domain
COL6A6	Collagen type VI alpha 6	Yes	No
MXRA8	Matrix remodeling associated 8	Yes	No
PLEKHF2	Pleckstrin homology and FYVE domain containing 2	Yes	No
RPRM	Reprimo, TP53 dependent G2 arrest mediator candidate	Yes	No
CDH4	Cadherin 4	No	No
PLEKHG1	Pleckstrin homology and RhoGEF domain containing G1	Yes	No
CAND1	Cullin associated and neddylation dissociated 1	Yes	No
MYO10	Myosin X	Yes	No
LRRC4C	Leucine rich repeat containing 4C	Yes	No
LRAT	Lecithin retinol acyltransferase	Yes	No
ANK3	Ankyrin 3, node of Ranvier	Yes	No
OLFM1	Olfactomedin 1	Yes	No
DCN	Decorin	Yes	Yes
NEURL1B	Neuralized E3 ubiquitin protein ligase 1B	Yes	No
PLEKHH2	Pleckstrin homology, MyTH4, and FERM domain containing H2	Yes	Yes
GLTSCR2	Glioma tumor suppressor candidate region gene 2	Yes	No
NDRG2	NDRG family member 2	Yes	No