abnormality of the periventricular white matter Gene Set
Genes
19 genes associated with the abnormality of the periventricular white matter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
AARS2
|
alanyl-tRNA synthetase 2, mitochondrial
|
|
AP4B1
|
adaptor-related protein complex 4, beta 1 subunit
|
|
ARHGAP31
|
Rho GTPase activating protein 31
|
|
CYP27A1
|
cytochrome P450, family 27, subfamily A, polypeptide 1
|
|
DDHD2
|
DDHD domain containing 2
|
|
FA2H
|
fatty acid 2-hydroxylase
|
|
GLUL
|
glutamate-ammonia ligase
|
|
LAMA1
|
laminin, alpha 1
|
|
LARGE
|
like-glycosyltransferase
|
|
MEF2C
|
myocyte enhancer factor 2C
|
|
OCRL
|
oculocerebrorenal syndrome of Lowe
|
|
PC
|
pyruvate carboxylase
|
|
PSAP
|
prosaposin
|
|
SEPSECS
|
Sep (O-phosphoserine) tRNA:Sec (selenocysteine) tRNA synthase
|
|
SHANK3
|
SH3 and multiple ankyrin repeat domains 3
|
|
SPG11
|
spastic paraplegia 11 (autosomal recessive)
|
|
SUMF1
|
sulfatase modifying factor 1
|
|
TREX1
|
three prime repair exonuclease 1
|
|
TSEN54
|
TSEN54 tRNA splicing endonuclease subunit
|
