| Symbol |
Name |
|
ADAMTS1
|
ADAM metallopeptidase with thrombospondin type 1 motif, 1
|
|
AGPAT2
|
1-acylglycerol-3-phosphate O-acyltransferase 2
|
|
AGT
|
angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
|
|
ALMS1
|
Alstrom syndrome protein 1
|
|
AMER1
|
APC membrane recruitment protein 1
|
|
ANK1
|
ankyrin 1, erythrocytic
|
|
ANKRD26
|
ankyrin repeat domain 26
|
|
AQP11
|
aquaporin 11
|
|
ARL3
|
ADP-ribosylation factor-like 3
|
|
ATP12A
|
ATPase, H+/K+ transporting, nongastric, alpha polypeptide
|
|
B9D1
|
B9 protein domain 1
|
|
BCAT2
|
branched chain amino-acid transaminase 2, mitochondrial
|
|
BCKDK
|
branched chain ketoacid dehydrogenase kinase
|
|
BCL2
|
B-cell CLL/lymphoma 2
|
|
BICC1
|
BicC family RNA binding protein 1
|
|
BMP4
|
bone morphogenetic protein 4
|
|
BSCL2
|
Berardinelli-Seip congenital lipodystrophy 2 (seipin)
|
|
CAV1
|
caveolin 1, caveolae protein, 22kDa
|
|
CD151
|
CD151 molecule (Raph blood group)
|
|
CDKN1A
|
cyclin-dependent kinase inhibitor 1A (p21, Cip1)
|
|
CDKN1B
|
cyclin-dependent kinase inhibitor 1B (p27, Kip1)
|
|
CXCR2
|
chemokine (C-X-C motif) receptor 2
|
|
CYP11B2
|
cytochrome P450, family 11, subfamily B, polypeptide 2
|
|
CYS1
|
cystin 1
|
|
DFNB31
|
deafness, autosomal recessive 31
|
|
ERAP1
|
endoplasmic reticulum aminopeptidase 1
|
|
FABP2
|
fatty acid binding protein 2, intestinal
|
|
FADS2
|
fatty acid desaturase 2
|
|
FAH
|
fumarylacetoacetate hydrolase (fumarylacetoacetase)
|
|
FAIM2
|
Fas apoptotic inhibitory molecule 2
|
|
FOXC1
|
forkhead box C1
|
|
G6PC
|
glucose-6-phosphatase, catalytic subunit
|
|
GCDH
|
glutaryl-CoA dehydrogenase
|
|
GDF15
|
growth differentiation factor 15
|
|
GDNF
|
glial cell derived neurotrophic factor
|
|
GPC3
|
glypican 3
|
|
GSTK1
|
glutathione S-transferase kappa 1
|
|
GSTZ1
|
glutathione S-transferase zeta 1
|
|
HP
|
haptoglobin
|
|
HPS1
|
Hermansky-Pudlak syndrome 1
|
|
HSD11B2
|
hydroxysteroid (11-beta) dehydrogenase 2
|
|
IFT88
|
intraflagellar transport 88
|
|
IGF2R
|
insulin-like growth factor 2 receptor
|
|
INVS
|
inversin
|
|
KLF3
|
Kruppel-like factor 3 (basic)
|
|
LAMA5
|
laminin, alpha 5
|
|
LEP
|
leptin
|
|
LHCGR
|
luteinizing hormone/choriogonadotropin receptor
|
|
LRRK2
|
leucine-rich repeat kinase 2
|
|
LYST
|
lysosomal trafficking regulator
|
|
MARVELD2
|
MARVEL domain containing 2
|
|
MGP
|
matrix Gla protein
|
|
MKS1
|
Meckel syndrome, type 1
|
|
MPV17
|
MpV17 mitochondrial inner membrane protein
|
|
MYO1E
|
myosin IE
|
|
NEK8
|
NIMA-related kinase 8
|
|
NPHP3
|
nephronophthisis 3 (adolescent)
|
|
NPHS1
|
nephrosis 1, congenital, Finnish type (nephrin)
|
|
OCA2
|
oculocutaneous albinism II
|
|
PKD1
|
polycystic kidney disease 1 (autosomal dominant)
|
|
PKD2
|
polycystic kidney disease 2 (autosomal dominant)
|
|
PKHD1
|
polycystic kidney and hepatic disease 1 (autosomal recessive)
|
|
PLCB1
|
phospholipase C, beta 1 (phosphoinositide-specific)
|
|
PLG
|
plasminogen
|
|
PLXNB1
|
plexin B1
|
|
PREP
|
prolyl endopeptidase
|
|
PTCD2
|
pentatricopeptide repeat domain 2
|
|
RDH16
|
retinol dehydrogenase 16 (all-trans)
|
|
RRM2B
|
ribonucleotide reductase M2 B (TP53 inducible)
|
|
SLC37A4
|
solute carrier family 37 (glucose-6-phosphate transporter), member 4
|
|
SPTB
|
spectrin, beta, erythrocytic
|
|
SPTBN1
|
spectrin, beta, non-erythrocytic 1
|
|
TIMP3
|
TIMP metallopeptidase inhibitor 3
|
|
TNS1
|
tensin 1
|
|
UBE2E2
|
ubiquitin-conjugating enzyme E2E 2
|
|
WWTR1
|
WW domain containing transcription regulator 1
|
|
XYLT2
|
xylosyltransferase II
|
|
ZMPSTE24
|
zinc metallopeptidase STE24
|
