abnormal hair laboratory examination Gene Set
Genes
15 genes associated with the abnormal hair laboratory examination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
ASL
|
argininosuccinate lyase
|
|
BCS1L
|
BC1 (ubiquinol-cytochrome c reductase) synthesis-like
|
|
CDH3
|
cadherin 3, type 1, P-cadherin (placental)
|
|
DSG4
|
desmoglein 4
|
|
FOXE1
|
forkhead box E1
|
|
HR
|
hair growth associated
|
|
KRT85
|
keratin 85, type II
|
|
MPLKIP
|
M-phase specific PLK1 interacting protein
|
|
PVRL1
|
poliovirus receptor-related 1 (herpesvirus entry mediator C)
|
|
PVRL4
|
poliovirus receptor-related 4
|
|
SKIV2L
|
superkiller viralicidic activity 2-like (S. cerevisiae)
|
|
ST14
|
suppression of tumorigenicity 14 (colon carcinoma)
|
|
TP63
|
tumor protein p63
|
|
TTC37
|
tetratricopeptide repeat domain 37
|
|
WRN
|
Werner syndrome, RecQ helicase-like
|
