prolonged neonatal jaundice Gene Set
Genes
16 genes associated with the prolonged neonatal jaundice phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
ADAMTS13
|
ADAM metallopeptidase with thrombospondin type 1 motif, 13
|
|
AMACR
|
alpha-methylacyl-CoA racemase
|
|
CDAN1
|
codanin 1
|
|
CIRH1A
|
cirrhosis, autosomal recessive 1A (cirhin)
|
|
G6PD
|
glucose-6-phosphate dehydrogenase
|
|
GALK1
|
galactokinase 1
|
|
JAG1
|
jagged 1
|
|
MPV17
|
MpV17 mitochondrial inner membrane protein
|
|
NPC1
|
Niemann-Pick disease, type C1
|
|
NPC2
|
Niemann-Pick disease, type C2
|
|
PEPD
|
peptidase D
|
|
PEX1
|
peroxisomal biogenesis factor 1
|
|
POU1F1
|
POU class 1 homeobox 1
|
|
RNU4ATAC
|
RNA, U4atac small nuclear (U12-dependent splicing)
|
|
SMPD1
|
sphingomyelin phosphodiesterase 1, acid lysosomal
|
|
TREX1
|
three prime repair exonuclease 1
|
