craniofacial abnormalities; growth disorders; learning disorders; syndrome Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description disease cluster belonging to disease group developmental (Genetic Association Database)
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Genes

14 genes associated with the disease craniofacial abnormalities; growth disorders; learning disorders; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ADAP2 ArfGAP with dual PH domains 2
ATAD5 ATPase family, AAA domain containing 5
CRLF3 cytokine receptor-like factor 3
DPRXP4 divergent-paired related homeobox pseudogene 4
LOC400590 uncharacterized LOC400590
LOC646021
LOC646030 leucine-rich repeat-containing protein 37A2-like
LRRC37B leucine rich repeat containing 37B
NF1 neurofibromin 1
RNF135 ring finger protein 135
RPS17P3 ribosomal protein S17 pseudogene 3
SH3GL1P2 SH3-domain GRB2-like 1 pseudogene 2
SUZ12P1 suppressor of zeste 12 homolog pseudogene 1
TEFM transcription elongation factor, mitochondrial