Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1a |
T |
A |
5: 8,788,702 (GRCm39) |
L1027* |
probably null |
Het |
Afap1l2 |
T |
C |
19: 56,906,427 (GRCm39) |
K491E |
probably damaging |
Het |
Ahr |
A |
T |
12: 35,561,164 (GRCm39) |
D150E |
probably damaging |
Het |
Arhgef1 |
T |
A |
7: 24,607,304 (GRCm39) |
L17Q |
probably damaging |
Het |
Bysl |
A |
G |
17: 47,915,242 (GRCm39) |
S169P |
|
Het |
C4b |
A |
T |
17: 34,948,404 (GRCm39) |
F1610I |
probably damaging |
Het |
Chtf8 |
C |
A |
8: 107,612,481 (GRCm39) |
A153S |
probably benign |
Het |
Ciapin1 |
C |
T |
8: 95,558,400 (GRCm39) |
|
probably null |
Het |
Cnnm1 |
A |
G |
19: 43,429,395 (GRCm39) |
E171G |
possibly damaging |
Het |
Crybb3 |
T |
C |
5: 113,225,407 (GRCm39) |
N155S |
probably benign |
Het |
Dclk3 |
T |
A |
9: 111,317,683 (GRCm39) |
M773K |
probably benign |
Het |
Ddx18 |
A |
T |
1: 121,489,267 (GRCm39) |
V260D |
probably damaging |
Het |
Dmxl2 |
T |
A |
9: 54,307,321 (GRCm39) |
N2216Y |
|
Het |
Epn2 |
T |
C |
11: 61,437,446 (GRCm39) |
E42G |
probably damaging |
Het |
Esrrg |
C |
A |
1: 187,878,605 (GRCm39) |
P229T |
probably benign |
Het |
Esrrg |
C |
A |
1: 187,878,606 (GRCm39) |
P229Q |
possibly damaging |
Het |
Ethe1 |
G |
T |
7: 24,305,643 (GRCm39) |
R130L |
probably benign |
Het |
Fgl2 |
G |
A |
5: 21,580,363 (GRCm39) |
C235Y |
probably damaging |
Het |
Fmnl1 |
C |
T |
11: 103,087,327 (GRCm39) |
T890M |
unknown |
Het |
Fsip2 |
C |
G |
2: 82,807,301 (GRCm39) |
P1207A |
probably benign |
Het |
Gc |
C |
T |
5: 89,593,165 (GRCm39) |
D85N |
possibly damaging |
Het |
Gfi1 |
G |
A |
5: 107,869,370 (GRCm39) |
R287W |
probably damaging |
Het |
Gm3629 |
T |
C |
14: 17,834,566 (GRCm39) |
|
probably null |
Het |
Hapln3 |
A |
G |
7: 78,771,712 (GRCm39) |
F59S |
probably benign |
Het |
Il24 |
G |
A |
1: 130,813,483 (GRCm39) |
T38I |
possibly damaging |
Het |
Izumo1 |
A |
G |
7: 45,276,583 (GRCm39) |
D382G |
probably benign |
Het |
Kdm5a |
T |
A |
6: 120,382,887 (GRCm39) |
Y739* |
probably null |
Het |
Kif2b |
T |
A |
11: 91,466,538 (GRCm39) |
I582F |
possibly damaging |
Het |
Klhdc1 |
A |
G |
12: 69,288,783 (GRCm39) |
Y31C |
probably damaging |
Het |
Lama1 |
G |
A |
17: 68,128,669 (GRCm39) |
E3009K |
|
Het |
Mad2l1bp |
G |
A |
17: 46,458,958 (GRCm39) |
R191C |
probably damaging |
Het |
Mark1 |
A |
C |
1: 184,644,261 (GRCm39) |
S468A |
probably damaging |
Het |
Mknk2 |
T |
A |
10: 80,504,823 (GRCm39) |
N236Y |
probably damaging |
Het |
Muc2 |
T |
A |
7: 141,287,983 (GRCm39) |
C251* |
probably null |
Het |
Nacad |
T |
C |
11: 6,552,252 (GRCm39) |
D313G |
probably damaging |
Het |
Neb |
G |
T |
2: 52,099,599 (GRCm39) |
D4750E |
probably benign |
Het |
Nlrp6 |
T |
C |
7: 140,506,332 (GRCm39) |
S758P |
probably damaging |
Het |
Nxt2 |
C |
T |
X: 141,020,747 (GRCm39) |
A118V |
possibly damaging |
Het |
Or13a28 |
A |
C |
7: 140,218,282 (GRCm39) |
I223L |
probably benign |
Het |
Or51b4 |
T |
C |
7: 103,530,569 (GRCm39) |
T294A |
possibly damaging |
Het |
Or8b3b |
A |
G |
9: 38,583,892 (GRCm39) |
F283L |
probably benign |
Het |
Oxtr |
A |
G |
6: 112,466,481 (GRCm39) |
V93A |
probably damaging |
Het |
Pbx3 |
C |
A |
2: 34,103,271 (GRCm39) |
D234Y |
probably damaging |
Het |
Pde4b |
A |
T |
4: 102,459,826 (GRCm39) |
T554S |
probably damaging |
Het |
Peg10 |
GC |
GCTCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
Pid1 |
A |
T |
1: 84,015,955 (GRCm39) |
Y151N |
probably damaging |
Het |
Plcd4 |
A |
G |
1: 74,591,307 (GRCm39) |
E234G |
possibly damaging |
Het |
Pou6f1 |
A |
G |
15: 100,478,789 (GRCm39) |
V373A |
probably benign |
Het |
Ppp1r12c |
T |
C |
7: 4,485,792 (GRCm39) |
K685E |
possibly damaging |
Het |
Rnf34 |
T |
A |
5: 122,999,957 (GRCm39) |
V71D |
probably damaging |
Het |
Rpap2 |
T |
G |
5: 107,746,156 (GRCm39) |
H11Q |
possibly damaging |
Het |
Skint2 |
A |
G |
4: 112,496,834 (GRCm39) |
T247A |
probably benign |
Het |
Stat5b |
T |
A |
11: 100,692,350 (GRCm39) |
N145Y |
probably damaging |
Het |
Sv2b |
A |
G |
7: 74,856,017 (GRCm39) |
L91P |
probably damaging |
Het |
Syt1 |
A |
G |
10: 108,340,376 (GRCm39) |
I314T |
probably damaging |
Het |
Tlk1 |
A |
T |
2: 70,572,502 (GRCm39) |
N355K |
probably benign |
Het |
Tnc |
C |
A |
4: 63,890,973 (GRCm39) |
M1636I |
probably benign |
Het |
Trank1 |
C |
A |
9: 111,162,843 (GRCm39) |
A34D |
probably damaging |
Het |
Unc13c |
A |
G |
9: 73,719,665 (GRCm39) |
I1001T |
probably benign |
Het |
Vdr |
T |
C |
15: 97,765,136 (GRCm39) |
D201G |
probably benign |
Het |
Vmn2r115 |
A |
T |
17: 23,564,307 (GRCm39) |
I160L |
probably benign |
Het |
Wdr81 |
C |
A |
11: 75,335,250 (GRCm39) |
R1772L |
probably damaging |
Het |
Zfp457 |
T |
C |
13: 67,442,068 (GRCm39) |
D169G |
probably benign |
Het |
|
Other mutations in Actl11 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01081:Actl11
|
APN |
9 |
107,806,181 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL01396:Actl11
|
APN |
9 |
107,805,964 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01622:Actl11
|
APN |
9 |
107,805,775 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01623:Actl11
|
APN |
9 |
107,805,775 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01660:Actl11
|
APN |
9 |
107,806,247 (GRCm39) |
missense |
probably benign |
|
IGL01912:Actl11
|
APN |
9 |
107,806,844 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02002:Actl11
|
APN |
9 |
107,806,529 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02266:Actl11
|
APN |
9 |
107,808,382 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL02535:Actl11
|
APN |
9 |
107,807,136 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02692:Actl11
|
APN |
9 |
107,806,507 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02744:Actl11
|
APN |
9 |
107,807,061 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02864:Actl11
|
APN |
9 |
107,806,186 (GRCm39) |
missense |
probably benign |
0.25 |
IGL03037:Actl11
|
APN |
9 |
107,807,294 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03085:Actl11
|
APN |
9 |
107,806,749 (GRCm39) |
missense |
probably damaging |
0.98 |
R0167:Actl11
|
UTSW |
9 |
107,806,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R0304:Actl11
|
UTSW |
9 |
107,806,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R0959:Actl11
|
UTSW |
9 |
107,808,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R1499:Actl11
|
UTSW |
9 |
107,808,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R1616:Actl11
|
UTSW |
9 |
107,809,135 (GRCm39) |
missense |
probably benign |
0.39 |
R1694:Actl11
|
UTSW |
9 |
107,807,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R1927:Actl11
|
UTSW |
9 |
107,806,736 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2081:Actl11
|
UTSW |
9 |
107,807,396 (GRCm39) |
missense |
probably benign |
|
R2939:Actl11
|
UTSW |
9 |
107,808,409 (GRCm39) |
missense |
possibly damaging |
0.84 |
R3427:Actl11
|
UTSW |
9 |
107,806,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R4812:Actl11
|
UTSW |
9 |
107,808,329 (GRCm39) |
missense |
probably damaging |
0.99 |
R4843:Actl11
|
UTSW |
9 |
107,806,691 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4972:Actl11
|
UTSW |
9 |
107,807,155 (GRCm39) |
missense |
probably benign |
0.07 |
R4989:Actl11
|
UTSW |
9 |
107,808,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R4996:Actl11
|
UTSW |
9 |
107,808,934 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5320:Actl11
|
UTSW |
9 |
107,808,203 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5546:Actl11
|
UTSW |
9 |
107,806,832 (GRCm39) |
missense |
probably benign |
0.00 |
R5810:Actl11
|
UTSW |
9 |
107,806,420 (GRCm39) |
missense |
probably benign |
0.23 |
R6302:Actl11
|
UTSW |
9 |
107,806,772 (GRCm39) |
missense |
probably benign |
0.12 |
R6412:Actl11
|
UTSW |
9 |
107,807,116 (GRCm39) |
missense |
probably benign |
0.01 |
R6835:Actl11
|
UTSW |
9 |
107,807,761 (GRCm39) |
missense |
probably benign |
|
R6891:Actl11
|
UTSW |
9 |
107,806,346 (GRCm39) |
missense |
probably benign |
0.03 |
R7195:Actl11
|
UTSW |
9 |
107,806,069 (GRCm39) |
nonsense |
probably null |
|
R7212:Actl11
|
UTSW |
9 |
107,805,856 (GRCm39) |
missense |
probably damaging |
0.99 |
R8478:Actl11
|
UTSW |
9 |
107,805,844 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8670:Actl11
|
UTSW |
9 |
107,805,959 (GRCm39) |
missense |
possibly damaging |
0.76 |
R8683:Actl11
|
UTSW |
9 |
107,806,065 (GRCm39) |
missense |
probably benign |
0.15 |
R9233:Actl11
|
UTSW |
9 |
107,807,900 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9280:Actl11
|
UTSW |
9 |
107,808,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R9361:Actl11
|
UTSW |
9 |
107,805,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R9565:Actl11
|
UTSW |
9 |
107,808,121 (GRCm39) |
missense |
possibly damaging |
0.92 |
X0024:Actl11
|
UTSW |
9 |
107,807,704 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Actl11
|
UTSW |
9 |
107,808,899 (GRCm39) |
missense |
probably benign |
0.20 |
|