Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcyap1r1 |
A |
G |
6: 55,456,257 (GRCm39) |
D215G |
possibly damaging |
Het |
Asb3 |
A |
T |
11: 30,948,326 (GRCm39) |
M40L |
probably damaging |
Het |
Aspg |
G |
A |
12: 112,093,123 (GRCm39) |
V547M |
possibly damaging |
Het |
Aspm |
T |
A |
1: 139,407,944 (GRCm39) |
L2277* |
probably null |
Het |
Atp7b |
A |
G |
8: 22,484,828 (GRCm39) |
S1295P |
probably benign |
Het |
Cdca2 |
A |
G |
14: 67,943,193 (GRCm39) |
S199P |
probably damaging |
Het |
Cdh1 |
A |
G |
8: 107,387,642 (GRCm39) |
E514G |
possibly damaging |
Het |
Cenpk |
G |
T |
13: 104,365,500 (GRCm39) |
|
probably benign |
Het |
Col6a5 |
C |
A |
9: 105,817,118 (GRCm39) |
V398L |
unknown |
Het |
Colec10 |
A |
T |
15: 54,326,002 (GRCm39) |
K277N |
probably damaging |
Het |
Cspg4 |
T |
A |
9: 56,805,164 (GRCm39) |
Y1992N |
possibly damaging |
Het |
Drd3 |
G |
T |
16: 43,641,683 (GRCm39) |
R333L |
probably benign |
Het |
Espl1 |
C |
T |
15: 102,207,342 (GRCm39) |
R269C |
probably benign |
Het |
Esr2 |
C |
T |
12: 76,212,252 (GRCm39) |
C188Y |
probably damaging |
Het |
Focad |
A |
G |
4: 88,267,112 (GRCm39) |
D1041G |
unknown |
Het |
Frem3 |
T |
C |
8: 81,337,911 (GRCm39) |
F68S |
possibly damaging |
Het |
Gapdh |
A |
G |
6: 125,139,634 (GRCm39) |
V212A |
probably damaging |
Het |
Gzmb |
T |
C |
14: 56,497,734 (GRCm39) |
K169E |
probably benign |
Het |
Hexd |
T |
A |
11: 121,102,880 (GRCm39) |
F33I |
possibly damaging |
Het |
Hsd3b6 |
T |
C |
3: 98,718,269 (GRCm39) |
I32V |
probably benign |
Het |
Jcad |
T |
C |
18: 4,673,372 (GRCm39) |
V378A |
probably benign |
Het |
Kcnmb2 |
T |
C |
3: 32,253,190 (GRCm39) |
S177P |
probably benign |
Het |
Lrriq1 |
A |
T |
10: 103,050,800 (GRCm39) |
S651T |
possibly damaging |
Het |
Map3k2 |
T |
C |
18: 32,340,593 (GRCm39) |
|
probably null |
Het |
Mib1 |
T |
G |
18: 10,802,282 (GRCm39) |
S870A |
probably benign |
Het |
Moap1 |
T |
A |
12: 102,708,871 (GRCm39) |
N226I |
probably damaging |
Het |
Moxd1 |
T |
A |
10: 24,176,186 (GRCm39) |
N547K |
probably damaging |
Het |
Mtmr9 |
A |
G |
14: 63,781,042 (GRCm39) |
V16A |
probably benign |
Het |
Nme1 |
T |
C |
11: 93,850,229 (GRCm39) |
Y151C |
probably damaging |
Het |
Nwd1 |
T |
C |
8: 73,408,653 (GRCm39) |
F879L |
probably benign |
Het |
Nynrin |
T |
G |
14: 56,101,335 (GRCm39) |
S335A |
probably benign |
Het |
Or52ac1 |
A |
T |
7: 104,245,796 (GRCm39) |
Y197* |
probably null |
Het |
Or5ac25 |
C |
A |
16: 59,181,826 (GRCm39) |
G252C |
probably damaging |
Het |
Or5b102 |
A |
T |
19: 13,041,348 (GRCm39) |
H191L |
probably benign |
Het |
Or5b99 |
A |
G |
19: 12,977,202 (GRCm39) |
N284S |
probably damaging |
Het |
Or8d23 |
T |
C |
9: 38,841,862 (GRCm39) |
Y132H |
probably damaging |
Het |
Or8g21 |
T |
C |
9: 38,905,928 (GRCm39) |
M268V |
probably benign |
Het |
Pcdhb21 |
A |
G |
18: 37,647,474 (GRCm39) |
E201G |
probably damaging |
Het |
Plscr1 |
T |
C |
9: 92,152,004 (GRCm39) |
V301A |
possibly damaging |
Het |
Psg28 |
A |
T |
7: 18,157,003 (GRCm39) |
S411T |
possibly damaging |
Het |
Rif1 |
T |
C |
2: 51,985,973 (GRCm39) |
W653R |
probably damaging |
Het |
Rnd3 |
T |
A |
2: 51,022,518 (GRCm39) |
I175L |
probably benign |
Het |
Rtn4 |
A |
G |
11: 29,656,791 (GRCm39) |
E199G |
possibly damaging |
Het |
Sgpp1 |
T |
C |
12: 75,763,344 (GRCm39) |
Y279C |
probably damaging |
Het |
Slc2a13 |
A |
G |
15: 91,160,382 (GRCm39) |
I524T |
probably damaging |
Het |
Speer4a2 |
A |
G |
5: 26,290,586 (GRCm39) |
|
probably null |
Het |
Spg11 |
C |
T |
2: 121,900,385 (GRCm39) |
V1556I |
probably benign |
Het |
Spopfm1 |
T |
A |
3: 94,173,855 (GRCm39) |
C288S |
probably benign |
Het |
Srebf2 |
C |
T |
15: 82,087,924 (GRCm39) |
R215* |
probably null |
Het |
Tdpoz8 |
G |
A |
3: 92,981,267 (GRCm39) |
C95Y |
probably damaging |
Het |
Tmem19 |
T |
C |
10: 115,183,179 (GRCm39) |
N147S |
possibly damaging |
Het |
Tpr |
T |
C |
1: 150,284,536 (GRCm39) |
S408P |
possibly damaging |
Het |
Trav13d-4 |
C |
T |
14: 53,310,618 (GRCm39) |
T53I |
probably damaging |
Het |
Trf |
T |
A |
9: 103,099,307 (GRCm39) |
R168W |
possibly damaging |
Het |
Trim11 |
A |
G |
11: 58,879,669 (GRCm39) |
K273R |
probably damaging |
Het |
Tsacc |
T |
A |
3: 88,190,247 (GRCm39) |
M68L |
probably benign |
Het |
Ttn |
T |
A |
2: 76,584,869 (GRCm39) |
M22110L |
probably benign |
Het |
Zfp160 |
G |
T |
17: 21,261,724 (GRCm39) |
G104V |
probably benign |
Het |
Zfp582 |
T |
C |
7: 6,357,266 (GRCm39) |
Y360H |
probably damaging |
Het |
Zranb1 |
G |
A |
7: 132,568,323 (GRCm39) |
R301H |
possibly damaging |
Het |
|
Other mutations in Cryzl2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00808:Cryzl2
|
APN |
1 |
157,298,246 (GRCm39) |
missense |
probably benign |
|
IGL01481:Cryzl2
|
APN |
1 |
157,298,309 (GRCm39) |
splice site |
probably null |
|
IGL01878:Cryzl2
|
APN |
1 |
157,299,970 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL02596:Cryzl2
|
APN |
1 |
157,292,539 (GRCm39) |
missense |
probably damaging |
1.00 |
G5030:Cryzl2
|
UTSW |
1 |
157,292,580 (GRCm39) |
nonsense |
probably null |
|
R0399:Cryzl2
|
UTSW |
1 |
157,289,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R0402:Cryzl2
|
UTSW |
1 |
157,292,014 (GRCm39) |
missense |
probably benign |
0.00 |
R0518:Cryzl2
|
UTSW |
1 |
157,292,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R0761:Cryzl2
|
UTSW |
1 |
157,293,294 (GRCm39) |
missense |
probably benign |
0.15 |
R1104:Cryzl2
|
UTSW |
1 |
157,298,174 (GRCm39) |
splice site |
probably benign |
|
R1471:Cryzl2
|
UTSW |
1 |
157,298,291 (GRCm39) |
missense |
probably benign |
0.01 |
R1773:Cryzl2
|
UTSW |
1 |
157,298,292 (GRCm39) |
missense |
probably benign |
0.01 |
R4752:Cryzl2
|
UTSW |
1 |
157,286,219 (GRCm39) |
splice site |
probably null |
|
R5046:Cryzl2
|
UTSW |
1 |
157,292,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R5389:Cryzl2
|
UTSW |
1 |
157,289,546 (GRCm39) |
nonsense |
probably null |
|
R5778:Cryzl2
|
UTSW |
1 |
157,298,357 (GRCm39) |
missense |
probably benign |
0.00 |
R7037:Cryzl2
|
UTSW |
1 |
157,298,318 (GRCm39) |
missense |
probably damaging |
0.99 |
R7099:Cryzl2
|
UTSW |
1 |
157,316,154 (GRCm39) |
critical splice donor site |
probably benign |
|
R7911:Cryzl2
|
UTSW |
1 |
157,299,925 (GRCm39) |
missense |
probably benign |
|
R8854:Cryzl2
|
UTSW |
1 |
157,286,370 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9618:Cryzl2
|
UTSW |
1 |
157,289,578 (GRCm39) |
missense |
probably benign |
0.00 |
R9667:Cryzl2
|
UTSW |
1 |
157,316,038 (GRCm39) |
missense |
probably benign |
|
Z1088:Cryzl2
|
UTSW |
1 |
157,293,359 (GRCm39) |
missense |
probably benign |
0.22 |
|