delayed brain development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description the delay or slower progress of the growth and differentiation of the brain (Mammalian Phenotype Ontology, MP_0001889)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001889
Similar Terms
Downloads & Tools

Genes

7 gene mutations causing the delayed brain development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CCNF cyclin F
DLC1 DLC1 Rho GTPase activating protein
NCOA6 nuclear receptor coactivator 6
PAFAH1B1 platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 (45kDa)
PEX5 peroxisomal biogenesis factor 5
SMG1 SMG1 phosphatidylinositol 3-kinase-related kinase
TCEB3 transcription elongation factor B (SIII), polypeptide 3 (110kDa, elongin A)