poor coordination Gene Set
Genes
23 genes associated with the poor coordination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
ARL6
|
ADP-ribosylation factor-like 6
|
|
BBS1
|
Bardet-Biedl syndrome 1
|
|
BBS10
|
Bardet-Biedl syndrome 10
|
|
BBS12
|
Bardet-Biedl syndrome 12
|
|
BBS2
|
Bardet-Biedl syndrome 2
|
|
BBS4
|
Bardet-Biedl syndrome 4
|
|
BBS5
|
Bardet-Biedl syndrome 5
|
|
BBS7
|
Bardet-Biedl syndrome 7
|
|
BBS9
|
Bardet-Biedl syndrome 9
|
|
CEP290
|
centrosomal protein 290kDa
|
|
CREBBP
|
CREB binding protein
|
|
ERCC4
|
excision repair cross-complementation group 4
|
|
IFT27
|
intraflagellar transport 27
|
|
LZTFL1
|
leucine zipper transcription factor-like 1
|
|
MKKS
|
McKusick-Kaufman syndrome
|
|
MKS1
|
Meckel syndrome, type 1
|
|
MTR
|
5-methyltetrahydrofolate-homocysteine methyltransferase
|
|
NSD1
|
nuclear receptor binding SET domain protein 1
|
|
SLC25A15
|
solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15
|
|
SLC6A8
|
solute carrier family 6 (neurotransmitter transporter), member 8
|
|
TRIM32
|
tripartite motif containing 32
|
|
TTC8
|
tetratricopeptide repeat domain 8
|
|
WDPCP
|
WD repeat containing planar cell polarity effector
|
