Androgen Insensitivity Syndrome
Watchlist
Retrieved
2022-04-26
Source
Trials
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Genes
AR,
FKBP4,
SMS,
PLAT,
RSS,
MTNR1B,
LBX1,
ESR1,
LEP,
MATN1,
IL6,
EGFR,
ESR2,
ADGRG6,
PAICS,
GART,
MTHFR,
C20orf181,
IGF1,
CALM1,
F5,
TPH1,
MT2A,
AMH,
MTNR1A,
MMP3,
TSPAN33,
TP53,
TMPRSS6,
BNC2
AR,
FKBP4,
SMS,
PLAT,
RSS,
MTNR1B,
LBX1,
ESR1,
LEP,
MATN1,
IL6,
EGFR,
ESR2,
ADGRG6,
PAICS,
GART,
MTHFR,
C20orf181,
IGF1,
CALM1,
F5,
TPH1,
MT2A,
AMH,
MTNR1A,
MMP3,
TSPAN33,
TP53,
TMPRSS6,
BNC2,
TNFRSF11B,
SIRT1,
NTF3,
SLC39A8,
NCOA2,
FBN1,
FBN2,
LEPR,
PYCARD,
PAX1,
PDXP,
GPER1,
GPX3,
SERPINE1,
TIMP2,
SHBG,
BRD2,
TGFB1,
SULT1E1,
MIR494,
VDR,
SRY,
STS,
VEGFA,
BDNF,
MIR15A,
EOS,
TP63,
ADIPOQ,
CST3,
IS1,
PITX1,
SOCS3,
POC5,
PON1,
CTNNB1,
PROM1,
KAT7,
GPR50,
PDAP1,
SIRT5,
TUSC2,
PAPOLA,
NDRG1,
TXN,
ADAMTS13,
MSC,
MRPS30,
AKR1C3,
CHL1,
BEST1,
VWF,
MYBBP1A,
USP8,
SMUG1,
UXT,
TNFSF11,
ASAP2,
GDF15,
AANAT,
TMEFF2,
MIR145,
DPP9,
NLRP3,
OCIAD2,
HJV,
NEAT1,
C17orf67,
SPATA21,
MIRLET7I,
MIR126,
MIR130A,
MIR134,
MIR183,
HECTD1,
MIR185,
MIR191,
MIR192,
MIR222,
MIR93,
PALM2AKAP2,
MT1IP,
MIR675,
CDKN2B-AS1,
MIR4300,
OCLN,
ADGRG7,
IL17RC,
DOT1L,
SPRY4,
SETBP1,
CNTNAP2,
PELP1,
CD274,
TBX21,
ASAP1,
ADIPOR1,
APH1A,
CLEC1B,
TNF,
MTPAP,
LAPTM4B,
SOX6,
MIB1,
PCDH10,
MIER1,
MID1IP1,
SOX17,
NUCKS1,
AHNAK,
IRX1,
FUZ,
VANGL1,
HSD17B7,
PSMD4,
TIMP1,
DLST,
CLTC,
COL4A2,
COL11A1,
COL11A2,
COMP,
MAP3K8,
CREBBP,
CRP,
CYP2C19,
DBP,
DMD,
CHI3L1,
DPP4,
DUSP2,
EPO,
F2,
F3,
FGFR3,
FGR,
FN1,
NR5A1,
GAD1,
CLU,
CDKN2A,
THRSP,
ASL,
ACP3,
ACTB,
ADRA1D,
ALB,
APC,
APOD,
APOE,
ARF6,
ARG1,
ARSF,
ATP2A2,
CDH13,
ATP2B4,
BGLAP,
BMP4,
BTF3P11,
CALCA,
CALM2,
CALM3,
CASP3,
RUNX2,
CD38,
GC,
GHSR,
MSH6,
ABO,
MT1L,
MT1X,
NRGN,
REG3A,
PAX3,
PBX1,
PLG,
PMCH,
MAPK7,
PSD,
RARB,
HDAC2,
PRPH2,
S100A12,
SFPQ,
SRSF1,
ITSN1,
SLC4A1,
SOX9,
SRD5A2,
STAT4,
TGM2,
MT1M,
MT1JP,
MT1H,
MT1G,
HGF,
HOXA10,
HSPG2,
IGFBP7,
IL1A,
IL1B,
IL5,
IL10,
ITGA2B,
KLK1,
KRAS,
LCN2,
LGALS1,
LGALS3,
LRPAP1,
KITLG,
MKI67,
MT1A,
MT1B,
MT1E,
MT1F,
H3P10
Drugs
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Registered!
Androgen insensitivity syndrome is a condition that affects sexual development before birth and during puberty. People with this condition are genetically male, with one X chromosome and one Y chromosome in each cell. Because their bodies are unable to respond to certain male sex hormones (called androgens), they may have some physical traits of a woman. Androgen insensitivity syndrome is caused by mutations in the AR gene and is inherited in an X-linked recessive pattern.