amyloidosis Gene Set
Genes
23 gene mutations causing the amyloidosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
| Symbol |
Name |
|
APCS
|
amyloid P component, serum
|
|
APOA2
|
apolipoprotein A-II
|
|
APOE
|
apolipoprotein E
|
|
APP
|
amyloid beta (A4) precursor protein
|
|
CAV1
|
caveolin 1, caveolae protein, 22kDa
|
|
CFH
|
complement factor H
|
|
CSF1
|
colony stimulating factor 1 (macrophage)
|
|
CST3
|
cystatin C
|
|
CTSB
|
cathepsin B
|
|
CTSK
|
cathepsin K
|
|
CTSV
|
cathepsin V
|
|
IDE
|
insulin-degrading enzyme
|
|
IL2
|
interleukin 2
|
|
LDLR
|
low density lipoprotein receptor
|
|
MME
|
membrane metallo-endopeptidase
|
|
NCKAP1L
|
NCK-associated protein 1-like
|
|
PIN1
|
peptidylprolyl cis/trans isomerase, NIMA-interacting 1
|
|
PSAP
|
prosaposin
|
|
RELB
|
v-rel avian reticuloendotheliosis viral oncogene homolog B
|
|
SORCS1
|
sortilin-related VPS10 domain containing receptor 1
|
|
SORL1
|
sortilin-related receptor, L(DLR class) A repeats containing
|
|
TRIB2
|
tribbles pseudokinase 2
|
|
ZDHHC13
|
zinc finger, DHHC-type containing 13
|
