Secondary Microcephaly Gene Set
Genes
13 genes associated with the disease Secondary Microcephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
| Symbol |
Name |
|
ARFGEF2
|
ADP-ribosylation factor guanine nucleotide-exchange factor 2 (brefeldin A-inhibited)
|
|
BPTF
|
bromodomain PHD finger transcription factor
|
|
DYRK1A
|
dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A
|
|
FOXG1
|
forkhead box G1
|
|
HUWE1
|
HECT, UBA and WWE domain containing 1, E3 ubiquitin protein ligase
|
|
KCNQ1
|
potassium channel, voltage gated KQT-like subfamily Q, member 1
|
|
MECP2
|
methyl CpG binding protein 2
|
|
MTM1
|
myotubularin 1
|
|
NACC1
|
nucleus accumbens associated 1, BEN and BTB (POZ) domain containing
|
|
PEX6
|
peroxisomal biogenesis factor 6
|
|
RARS2
|
arginyl-tRNA synthetase 2, mitochondrial
|
|
RUSC2
|
RUN and SH3 domain containing 2
|
|
SLC9A6
|
solute carrier family 9, subfamily A (NHE6, cation proton antiporter 6), member 6
|
