Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acp6 |
T |
C |
3: 97,075,891 (GRCm39) |
|
probably null |
Het |
Adam33 |
C |
A |
2: 130,896,399 (GRCm39) |
G437C |
probably damaging |
Het |
Aldh1a1 |
T |
A |
19: 20,579,377 (GRCm39) |
M1K |
probably null |
Het |
Amotl2 |
C |
A |
9: 102,597,718 (GRCm39) |
P126Q |
probably damaging |
Het |
Ap1g1 |
T |
A |
8: 110,580,275 (GRCm39) |
M576K |
possibly damaging |
Het |
Apob |
C |
A |
12: 8,040,406 (GRCm39) |
A581E |
probably damaging |
Het |
Asb7 |
A |
T |
7: 66,328,907 (GRCm39) |
D44E |
probably damaging |
Het |
Bcl2 |
G |
A |
1: 106,640,292 (GRCm39) |
R107C |
probably damaging |
Het |
C9orf72 |
G |
A |
4: 35,193,257 (GRCm39) |
T232I |
probably benign |
Het |
Ccdc65 |
A |
T |
15: 98,615,348 (GRCm39) |
H118L |
probably benign |
Het |
Cdc25b |
A |
G |
2: 131,039,204 (GRCm39) |
E523G |
probably damaging |
Het |
Cdk11b |
A |
G |
4: 155,731,999 (GRCm39) |
|
probably benign |
Het |
Cilk1 |
G |
T |
9: 78,062,799 (GRCm39) |
|
probably null |
Het |
Clec1b |
A |
G |
6: 129,378,570 (GRCm39) |
|
probably benign |
Het |
Cntrl |
A |
G |
2: 35,017,392 (GRCm39) |
T400A |
probably benign |
Het |
Cpne4 |
T |
G |
9: 104,899,481 (GRCm39) |
|
probably null |
Het |
Cyp2j6 |
T |
A |
4: 96,419,985 (GRCm39) |
R249* |
probably null |
Het |
Dock2 |
T |
C |
11: 34,579,380 (GRCm39) |
I678V |
probably benign |
Het |
Dqx1 |
C |
T |
6: 83,036,407 (GRCm39) |
|
probably benign |
Het |
Dsp |
A |
T |
13: 38,377,326 (GRCm39) |
K1704* |
probably null |
Het |
Eif2b2 |
T |
C |
12: 85,266,957 (GRCm39) |
F121S |
probably benign |
Het |
Ephx4 |
T |
C |
5: 107,561,379 (GRCm39) |
V69A |
possibly damaging |
Het |
Epn2 |
T |
C |
11: 61,426,134 (GRCm39) |
Q281R |
probably damaging |
Het |
Fgf3 |
A |
C |
7: 144,396,547 (GRCm39) |
D187A |
probably damaging |
Het |
Galnt18 |
C |
A |
7: 111,378,506 (GRCm39) |
|
probably benign |
Het |
Gm4871 |
C |
T |
5: 144,968,402 (GRCm39) |
|
probably benign |
Het |
Inpp4b |
T |
C |
8: 82,768,528 (GRCm39) |
I679T |
possibly damaging |
Het |
Itpkb |
A |
G |
1: 180,245,820 (GRCm39) |
E779G |
probably damaging |
Het |
Itsn1 |
G |
A |
16: 91,696,477 (GRCm39) |
V27M |
probably damaging |
Het |
Lrp2 |
C |
A |
2: 69,355,578 (GRCm39) |
R422L |
probably damaging |
Het |
Mprip |
T |
C |
11: 59,650,561 (GRCm39) |
S1422P |
probably damaging |
Het |
Mro |
A |
T |
18: 74,009,860 (GRCm39) |
Q176L |
probably benign |
Het |
Mrpl12 |
A |
G |
11: 120,379,229 (GRCm39) |
E192G |
probably damaging |
Het |
Myo5b |
A |
T |
18: 74,862,025 (GRCm39) |
|
probably benign |
Het |
Ncam2 |
G |
T |
16: 80,997,772 (GRCm39) |
|
probably benign |
Het |
Nip7 |
T |
C |
8: 107,783,949 (GRCm39) |
L63P |
probably damaging |
Het |
Nsd3 |
T |
C |
8: 26,138,450 (GRCm39) |
|
probably benign |
Het |
Nup98 |
A |
T |
7: 101,788,004 (GRCm39) |
V1022D |
probably benign |
Het |
Or2y1e |
T |
A |
11: 49,218,744 (GRCm39) |
C169S |
probably damaging |
Het |
Or5d43 |
A |
G |
2: 88,104,559 (GRCm39) |
V278A |
possibly damaging |
Het |
Or5h22 |
A |
G |
16: 58,894,633 (GRCm39) |
I270T |
probably benign |
Het |
Or7g28 |
A |
T |
9: 19,272,177 (GRCm39) |
L158* |
probably null |
Het |
P4ha2 |
T |
C |
11: 54,008,434 (GRCm39) |
Y214H |
possibly damaging |
Het |
Pacrg |
A |
T |
17: 10,795,407 (GRCm39) |
F184L |
possibly damaging |
Het |
Parpbp |
T |
A |
10: 87,929,569 (GRCm39) |
R426S |
probably damaging |
Het |
Pcdhb5 |
T |
A |
18: 37,454,359 (GRCm39) |
Y246* |
probably null |
Het |
Pik3cg |
T |
A |
12: 32,244,770 (GRCm39) |
T895S |
probably damaging |
Het |
Prkch |
T |
C |
12: 73,738,426 (GRCm39) |
Y178H |
probably benign |
Het |
Rusc2 |
G |
T |
4: 43,425,486 (GRCm39) |
R1197L |
probably damaging |
Het |
Svep1 |
T |
C |
4: 58,054,700 (GRCm39) |
E3296G |
possibly damaging |
Het |
Svs3a |
A |
G |
2: 164,131,801 (GRCm39) |
K123R |
probably benign |
Het |
Sycp2l |
A |
G |
13: 41,304,006 (GRCm39) |
|
probably null |
Het |
Syne3 |
T |
C |
12: 104,909,685 (GRCm39) |
H717R |
probably benign |
Het |
Tiprl |
A |
G |
1: 165,050,092 (GRCm39) |
|
probably null |
Het |
Trim24 |
T |
G |
6: 37,892,130 (GRCm39) |
V151G |
possibly damaging |
Het |
Trim33 |
T |
C |
3: 103,234,217 (GRCm39) |
V56A |
possibly damaging |
Het |
Trim67 |
C |
A |
8: 125,521,397 (GRCm39) |
T253K |
probably benign |
Het |
Trip12 |
T |
C |
1: 84,703,928 (GRCm39) |
E698G |
probably damaging |
Het |
Tspan14 |
T |
C |
14: 40,637,353 (GRCm39) |
D145G |
probably damaging |
Het |
Ushbp1 |
G |
A |
8: 71,847,021 (GRCm39) |
Q204* |
probably null |
Het |
Vmn1r71 |
G |
C |
7: 10,482,019 (GRCm39) |
S223C |
possibly damaging |
Het |
Vmn2r75 |
G |
T |
7: 85,814,721 (GRCm39) |
N257K |
probably benign |
Het |
Washc4 |
T |
C |
10: 83,394,598 (GRCm39) |
|
probably benign |
Het |
Zc3h7b |
G |
A |
15: 81,666,169 (GRCm39) |
D560N |
probably damaging |
Het |
Zscan21 |
T |
C |
5: 138,123,402 (GRCm39) |
V27A |
probably benign |
Het |
Zzef1 |
A |
C |
11: 72,813,937 (GRCm39) |
E2842A |
probably damaging |
Het |
|
Other mutations in Mmp25 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02814:Mmp25
|
APN |
17 |
23,858,736 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02893:Mmp25
|
APN |
17 |
23,863,025 (GRCm39) |
missense |
probably damaging |
1.00 |
R0478:Mmp25
|
UTSW |
17 |
23,851,756 (GRCm39) |
missense |
probably benign |
0.08 |
R1829:Mmp25
|
UTSW |
17 |
23,858,997 (GRCm39) |
missense |
probably benign |
0.00 |
R2005:Mmp25
|
UTSW |
17 |
23,859,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R2151:Mmp25
|
UTSW |
17 |
23,850,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R2153:Mmp25
|
UTSW |
17 |
23,850,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R2154:Mmp25
|
UTSW |
17 |
23,850,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R2937:Mmp25
|
UTSW |
17 |
23,863,765 (GRCm39) |
missense |
probably benign |
0.00 |
R4418:Mmp25
|
UTSW |
17 |
23,863,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R4667:Mmp25
|
UTSW |
17 |
23,863,581 (GRCm39) |
missense |
probably benign |
0.00 |
R4905:Mmp25
|
UTSW |
17 |
23,863,022 (GRCm39) |
nonsense |
probably null |
|
R5535:Mmp25
|
UTSW |
17 |
23,863,734 (GRCm39) |
missense |
probably benign |
|
R5592:Mmp25
|
UTSW |
17 |
23,859,176 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5888:Mmp25
|
UTSW |
17 |
23,850,048 (GRCm39) |
missense |
probably damaging |
1.00 |
R6261:Mmp25
|
UTSW |
17 |
23,849,768 (GRCm39) |
missense |
possibly damaging |
0.61 |
R6263:Mmp25
|
UTSW |
17 |
23,849,768 (GRCm39) |
missense |
possibly damaging |
0.61 |
R6264:Mmp25
|
UTSW |
17 |
23,849,768 (GRCm39) |
missense |
possibly damaging |
0.61 |
R6571:Mmp25
|
UTSW |
17 |
23,858,870 (GRCm39) |
missense |
probably benign |
0.17 |
R7172:Mmp25
|
UTSW |
17 |
23,863,762 (GRCm39) |
missense |
probably benign |
|
R7467:Mmp25
|
UTSW |
17 |
23,863,756 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8109:Mmp25
|
UTSW |
17 |
23,863,768 (GRCm39) |
missense |
probably benign |
0.00 |
R9300:Mmp25
|
UTSW |
17 |
23,851,728 (GRCm39) |
missense |
probably benign |
0.05 |
R9734:Mmp25
|
UTSW |
17 |
23,850,834 (GRCm39) |
missense |
possibly damaging |
0.94 |
T0722:Mmp25
|
UTSW |
17 |
23,850,192 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1176:Mmp25
|
UTSW |
17 |
23,849,633 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Mmp25
|
UTSW |
17 |
23,863,111 (GRCm39) |
missense |
possibly damaging |
0.76 |
|