Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb11 |
C |
A |
2: 69,073,842 (GRCm39) |
A1228S |
probably damaging |
Het |
Adamts12 |
G |
A |
15: 11,215,696 (GRCm39) |
R239K |
probably benign |
Het |
Akap6 |
A |
G |
12: 53,187,338 (GRCm39) |
D1584G |
probably damaging |
Het |
Asns |
A |
G |
6: 7,685,184 (GRCm39) |
C158R |
probably damaging |
Het |
Atr |
T |
C |
9: 95,753,540 (GRCm39) |
L714P |
probably damaging |
Het |
Ccdc126 |
G |
T |
6: 49,311,134 (GRCm39) |
E47D |
probably benign |
Het |
Cemip |
T |
C |
7: 83,646,500 (GRCm39) |
S183G |
probably damaging |
Het |
Cntn3 |
A |
G |
6: 102,176,321 (GRCm39) |
|
probably benign |
Het |
Cyp11b2 |
G |
T |
15: 74,725,038 (GRCm39) |
N270K |
probably benign |
Het |
Ephx2 |
A |
G |
14: 66,341,173 (GRCm39) |
|
probably null |
Het |
Fcho2 |
G |
A |
13: 98,867,414 (GRCm39) |
T683I |
probably damaging |
Het |
Grm7 |
G |
A |
6: 111,335,278 (GRCm39) |
C563Y |
probably damaging |
Het |
Hmcn1 |
T |
C |
1: 150,579,932 (GRCm39) |
N1935S |
probably benign |
Het |
Hus1b |
A |
G |
13: 31,130,900 (GRCm39) |
L253S |
probably benign |
Het |
Kmt5b |
T |
C |
19: 3,843,181 (GRCm39) |
Y93H |
probably damaging |
Het |
Krt73 |
A |
T |
15: 101,710,456 (GRCm39) |
S93T |
probably benign |
Het |
Lrp8 |
T |
C |
4: 107,727,306 (GRCm39) |
V917A |
probably benign |
Het |
Map2k6 |
C |
T |
11: 110,383,409 (GRCm39) |
T106M |
probably damaging |
Het |
Ncor1 |
A |
G |
11: 62,235,463 (GRCm39) |
S664P |
probably damaging |
Het |
Nmt1 |
C |
T |
11: 102,943,116 (GRCm39) |
T157I |
probably benign |
Het |
Nup160 |
T |
C |
2: 90,560,051 (GRCm39) |
S1259P |
probably damaging |
Het |
Pak1 |
C |
T |
7: 97,560,322 (GRCm39) |
A523V |
probably damaging |
Het |
Parpbp |
A |
C |
10: 87,979,898 (GRCm39) |
S19R |
probably benign |
Het |
Pdzd2 |
G |
T |
15: 12,376,382 (GRCm39) |
T1251N |
possibly damaging |
Het |
Phaf1 |
T |
A |
8: 105,966,341 (GRCm39) |
I105N |
probably damaging |
Het |
Pitpnm3 |
A |
T |
11: 72,010,965 (GRCm39) |
N22K |
probably benign |
Het |
Pkn1 |
G |
T |
8: 84,407,854 (GRCm39) |
C418* |
probably null |
Het |
Pkn2 |
A |
G |
3: 142,509,424 (GRCm39) |
F723L |
probably damaging |
Het |
Pkp4 |
C |
T |
2: 59,142,073 (GRCm39) |
R459* |
probably null |
Het |
Ptprz1 |
A |
G |
6: 23,002,502 (GRCm39) |
T1531A |
probably benign |
Het |
Rad1 |
C |
A |
15: 10,493,361 (GRCm39) |
Q263K |
probably benign |
Het |
Sh2d6 |
C |
A |
6: 72,490,961 (GRCm39) |
G307* |
probably null |
Het |
Slc52a3 |
T |
A |
2: 151,847,811 (GRCm39) |
N306K |
probably damaging |
Het |
Spock3 |
A |
T |
8: 63,698,232 (GRCm39) |
R195* |
probably null |
Het |
Stil |
A |
G |
4: 114,871,359 (GRCm39) |
S310G |
probably benign |
Het |
Wbp1l |
T |
A |
19: 46,640,959 (GRCm39) |
C80* |
probably null |
Het |
Wnt2b |
A |
G |
3: 104,854,408 (GRCm39) |
V350A |
probably benign |
Het |
|
Other mutations in Prex1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00161:Prex1
|
APN |
2 |
166,480,321 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00309:Prex1
|
APN |
2 |
166,451,743 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00953:Prex1
|
APN |
2 |
166,480,329 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00961:Prex1
|
APN |
2 |
166,427,656 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01300:Prex1
|
APN |
2 |
166,480,327 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL01318:Prex1
|
APN |
2 |
166,411,260 (GRCm39) |
splice site |
probably benign |
|
IGL01753:Prex1
|
APN |
2 |
166,444,802 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01819:Prex1
|
APN |
2 |
166,463,165 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02251:Prex1
|
APN |
2 |
166,419,806 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02326:Prex1
|
APN |
2 |
166,463,105 (GRCm39) |
missense |
probably benign |
0.35 |
IGL02366:Prex1
|
APN |
2 |
166,422,347 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02414:Prex1
|
APN |
2 |
166,451,748 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02660:Prex1
|
APN |
2 |
166,435,787 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02666:Prex1
|
APN |
2 |
166,414,909 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02874:Prex1
|
APN |
2 |
166,426,967 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02935:Prex1
|
APN |
2 |
166,412,265 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03179:Prex1
|
APN |
2 |
166,427,114 (GRCm39) |
missense |
probably benign |
0.31 |
R0207:Prex1
|
UTSW |
2 |
166,427,818 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0415:Prex1
|
UTSW |
2 |
166,428,619 (GRCm39) |
unclassified |
probably benign |
|
R0420:Prex1
|
UTSW |
2 |
166,431,491 (GRCm39) |
missense |
probably benign |
0.13 |
R0449:Prex1
|
UTSW |
2 |
166,411,297 (GRCm39) |
missense |
probably benign |
0.16 |
R0458:Prex1
|
UTSW |
2 |
166,427,743 (GRCm39) |
missense |
probably damaging |
0.99 |
R0927:Prex1
|
UTSW |
2 |
166,428,457 (GRCm39) |
missense |
probably benign |
0.01 |
R1299:Prex1
|
UTSW |
2 |
166,427,827 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1414:Prex1
|
UTSW |
2 |
166,435,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R1440:Prex1
|
UTSW |
2 |
166,422,383 (GRCm39) |
missense |
probably damaging |
0.98 |
R1506:Prex1
|
UTSW |
2 |
166,429,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R1725:Prex1
|
UTSW |
2 |
166,443,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R1831:Prex1
|
UTSW |
2 |
166,427,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R1883:Prex1
|
UTSW |
2 |
166,425,192 (GRCm39) |
missense |
probably benign |
0.20 |
R1896:Prex1
|
UTSW |
2 |
166,428,574 (GRCm39) |
missense |
probably benign |
0.01 |
R2022:Prex1
|
UTSW |
2 |
166,417,534 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2091:Prex1
|
UTSW |
2 |
166,411,285 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2258:Prex1
|
UTSW |
2 |
166,429,077 (GRCm39) |
missense |
probably benign |
0.00 |
R2263:Prex1
|
UTSW |
2 |
166,430,988 (GRCm39) |
splice site |
probably benign |
|
R2276:Prex1
|
UTSW |
2 |
166,419,875 (GRCm39) |
missense |
probably benign |
0.34 |
R2279:Prex1
|
UTSW |
2 |
166,419,875 (GRCm39) |
missense |
probably benign |
0.34 |
R2680:Prex1
|
UTSW |
2 |
166,443,692 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3024:Prex1
|
UTSW |
2 |
166,430,956 (GRCm39) |
missense |
probably benign |
0.04 |
R3421:Prex1
|
UTSW |
2 |
166,459,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R3614:Prex1
|
UTSW |
2 |
166,451,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R4244:Prex1
|
UTSW |
2 |
166,412,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R4605:Prex1
|
UTSW |
2 |
166,555,464 (GRCm39) |
missense |
probably benign |
0.45 |
R4685:Prex1
|
UTSW |
2 |
166,480,252 (GRCm39) |
missense |
probably damaging |
0.97 |
R4787:Prex1
|
UTSW |
2 |
166,480,260 (GRCm39) |
missense |
probably benign |
0.01 |
R4796:Prex1
|
UTSW |
2 |
166,434,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R4825:Prex1
|
UTSW |
2 |
166,427,777 (GRCm39) |
nonsense |
probably null |
|
R4955:Prex1
|
UTSW |
2 |
166,415,143 (GRCm39) |
missense |
probably damaging |
0.99 |
R5046:Prex1
|
UTSW |
2 |
166,414,883 (GRCm39) |
missense |
probably benign |
0.00 |
R5095:Prex1
|
UTSW |
2 |
166,423,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R5408:Prex1
|
UTSW |
2 |
166,417,573 (GRCm39) |
small insertion |
probably benign |
|
R5462:Prex1
|
UTSW |
2 |
166,486,728 (GRCm39) |
missense |
probably benign |
0.02 |
R5535:Prex1
|
UTSW |
2 |
166,422,193 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5777:Prex1
|
UTSW |
2 |
166,428,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R5813:Prex1
|
UTSW |
2 |
166,425,127 (GRCm39) |
missense |
probably benign |
|
R5860:Prex1
|
UTSW |
2 |
166,486,604 (GRCm39) |
intron |
probably benign |
|
R5984:Prex1
|
UTSW |
2 |
166,427,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R6009:Prex1
|
UTSW |
2 |
166,423,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R6174:Prex1
|
UTSW |
2 |
166,414,883 (GRCm39) |
missense |
probably benign |
0.00 |
R6345:Prex1
|
UTSW |
2 |
166,414,880 (GRCm39) |
missense |
probably null |
0.81 |
R6897:Prex1
|
UTSW |
2 |
166,423,913 (GRCm39) |
missense |
probably damaging |
0.99 |
R6935:Prex1
|
UTSW |
2 |
166,441,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R7025:Prex1
|
UTSW |
2 |
166,455,107 (GRCm39) |
small insertion |
probably benign |
|
R7037:Prex1
|
UTSW |
2 |
166,429,100 (GRCm39) |
missense |
probably benign |
0.05 |
R7076:Prex1
|
UTSW |
2 |
166,475,302 (GRCm39) |
missense |
probably damaging |
0.99 |
R7181:Prex1
|
UTSW |
2 |
166,412,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R7361:Prex1
|
UTSW |
2 |
166,555,490 (GRCm39) |
missense |
probably benign |
0.04 |
R7381:Prex1
|
UTSW |
2 |
166,429,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R7721:Prex1
|
UTSW |
2 |
166,419,810 (GRCm39) |
nonsense |
probably null |
|
R7763:Prex1
|
UTSW |
2 |
166,555,629 (GRCm39) |
missense |
unknown |
|
R7809:Prex1
|
UTSW |
2 |
166,415,164 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7915:Prex1
|
UTSW |
2 |
166,463,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R7971:Prex1
|
UTSW |
2 |
166,423,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R7998:Prex1
|
UTSW |
2 |
166,428,965 (GRCm39) |
critical splice donor site |
probably null |
|
R8029:Prex1
|
UTSW |
2 |
166,417,523 (GRCm39) |
missense |
probably benign |
0.01 |
R8193:Prex1
|
UTSW |
2 |
166,435,780 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8352:Prex1
|
UTSW |
2 |
166,431,493 (GRCm39) |
missense |
probably benign |
0.05 |
R8452:Prex1
|
UTSW |
2 |
166,431,493 (GRCm39) |
missense |
probably benign |
0.05 |
R8927:Prex1
|
UTSW |
2 |
166,426,995 (GRCm39) |
missense |
probably damaging |
0.97 |
R8928:Prex1
|
UTSW |
2 |
166,426,995 (GRCm39) |
missense |
probably damaging |
0.97 |
R9021:Prex1
|
UTSW |
2 |
166,432,429 (GRCm39) |
missense |
possibly damaging |
0.47 |
R9070:Prex1
|
UTSW |
2 |
166,427,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R9213:Prex1
|
UTSW |
2 |
166,417,669 (GRCm39) |
missense |
probably damaging |
0.99 |
R9511:Prex1
|
UTSW |
2 |
166,413,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R9514:Prex1
|
UTSW |
2 |
166,419,896 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9529:Prex1
|
UTSW |
2 |
166,431,518 (GRCm39) |
missense |
probably damaging |
1.00 |
X0065:Prex1
|
UTSW |
2 |
166,428,545 (GRCm39) |
missense |
probably benign |
|
Z1176:Prex1
|
UTSW |
2 |
166,414,890 (GRCm39) |
nonsense |
probably null |
|
Z1177:Prex1
|
UTSW |
2 |
166,434,148 (GRCm39) |
missense |
probably damaging |
0.98 |
|