Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahnak |
G |
A |
19: 8,994,098 (GRCm39) |
M5127I |
probably benign |
Het |
Akr1c13 |
T |
C |
13: 4,244,111 (GRCm39) |
Y55H |
probably damaging |
Het |
Armh3 |
A |
T |
19: 45,922,307 (GRCm39) |
|
probably null |
Het |
Atp2b2 |
C |
T |
6: 113,750,349 (GRCm39) |
R625H |
probably damaging |
Het |
Bpifb2 |
T |
C |
2: 153,720,439 (GRCm39) |
V66A |
probably benign |
Het |
Ccdc33 |
T |
C |
9: 57,936,046 (GRCm39) |
T950A |
possibly damaging |
Het |
Ceacam19 |
A |
T |
7: 19,616,557 (GRCm39) |
|
probably null |
Het |
Cenpn |
T |
A |
8: 117,667,559 (GRCm39) |
|
probably benign |
Het |
Ces1f |
A |
T |
8: 93,998,517 (GRCm39) |
Y160N |
possibly damaging |
Het |
Clca3a1 |
A |
C |
3: 144,710,615 (GRCm39) |
S863A |
probably benign |
Het |
Cntrl |
T |
A |
2: 35,045,291 (GRCm39) |
I781K |
possibly damaging |
Het |
Dock4 |
C |
T |
12: 40,754,480 (GRCm39) |
R490W |
probably damaging |
Het |
Evpl |
T |
A |
11: 116,118,549 (GRCm39) |
Q686L |
probably damaging |
Het |
Fbxw10 |
A |
G |
11: 62,738,282 (GRCm39) |
S59G |
probably benign |
Het |
Glb1l2 |
A |
G |
9: 26,681,047 (GRCm39) |
V218A |
possibly damaging |
Het |
Gpatch1 |
A |
T |
7: 34,980,801 (GRCm39) |
|
probably benign |
Het |
Grin2c |
G |
A |
11: 115,141,472 (GRCm39) |
P882L |
probably damaging |
Het |
H2-Ob |
C |
A |
17: 34,461,588 (GRCm39) |
T109N |
probably damaging |
Het |
Ipo8 |
A |
G |
6: 148,723,225 (GRCm39) |
V64A |
possibly damaging |
Het |
Jpt2 |
C |
A |
17: 25,167,647 (GRCm39) |
A101S |
probably benign |
Het |
Lamc1 |
C |
A |
1: 153,110,326 (GRCm39) |
Q1116H |
possibly damaging |
Het |
Lamc1 |
T |
C |
1: 153,110,358 (GRCm39) |
S1106G |
probably benign |
Het |
Lamc1 |
T |
G |
1: 153,110,341 (GRCm39) |
Q1111H |
probably damaging |
Het |
Large1 |
A |
G |
8: 73,775,107 (GRCm39) |
|
probably benign |
Het |
Lig4 |
A |
T |
8: 10,023,012 (GRCm39) |
V256E |
possibly damaging |
Het |
Mpz |
C |
A |
1: 170,986,343 (GRCm39) |
Q86K |
possibly damaging |
Het |
Mrps24 |
A |
G |
11: 5,654,684 (GRCm39) |
V90A |
possibly damaging |
Het |
Mtdh |
A |
G |
15: 34,116,528 (GRCm39) |
|
probably benign |
Het |
Mtor |
T |
C |
4: 148,547,367 (GRCm39) |
V450A |
probably benign |
Het |
Mycbpap |
A |
G |
11: 94,402,449 (GRCm39) |
|
probably null |
Het |
Myo6 |
T |
A |
9: 80,169,656 (GRCm39) |
|
probably benign |
Het |
Myom1 |
A |
T |
17: 71,428,131 (GRCm39) |
I1450F |
probably damaging |
Het |
Nbas |
T |
A |
12: 13,532,634 (GRCm39) |
S1781T |
probably benign |
Het |
Nedd1 |
T |
C |
10: 92,555,476 (GRCm39) |
E3G |
probably damaging |
Het |
Nt5c3 |
T |
C |
6: 56,863,734 (GRCm39) |
T149A |
probably benign |
Het |
Or5p56 |
A |
G |
7: 107,589,740 (GRCm39) |
H56R |
probably benign |
Het |
Osbp2 |
G |
A |
11: 3,661,882 (GRCm39) |
|
probably benign |
Het |
Paip1 |
T |
C |
13: 119,566,854 (GRCm39) |
S54P |
possibly damaging |
Het |
Pole2 |
G |
A |
12: 69,254,703 (GRCm39) |
L381F |
probably benign |
Het |
Prdm14 |
G |
T |
1: 13,195,968 (GRCm39) |
A31E |
probably benign |
Het |
Ptpn14 |
C |
T |
1: 189,568,637 (GRCm39) |
|
probably benign |
Het |
Rims2 |
A |
G |
15: 39,543,021 (GRCm39) |
|
probably benign |
Het |
Rnf20 |
A |
G |
4: 49,638,197 (GRCm39) |
N103S |
possibly damaging |
Het |
Sema3g |
T |
A |
14: 30,942,861 (GRCm39) |
|
probably benign |
Het |
Slc30a6 |
T |
C |
17: 74,722,640 (GRCm39) |
S236P |
possibly damaging |
Het |
Slc5a1 |
T |
C |
5: 33,315,421 (GRCm39) |
|
probably benign |
Het |
Snx25 |
A |
T |
8: 46,577,119 (GRCm39) |
M1K |
probably null |
Het |
Synpo2 |
A |
G |
3: 122,906,835 (GRCm39) |
V827A |
probably benign |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Trak2 |
A |
T |
1: 58,942,820 (GRCm39) |
M862K |
probably benign |
Het |
Twnk |
T |
C |
19: 44,998,693 (GRCm39) |
|
probably benign |
Het |
Tymp |
T |
C |
15: 89,259,021 (GRCm39) |
K221R |
probably damaging |
Het |
Uaca |
C |
A |
9: 60,779,341 (GRCm39) |
Q1243K |
possibly damaging |
Het |
Vwa8 |
T |
C |
14: 79,232,016 (GRCm39) |
|
probably benign |
Het |
Wnt4 |
C |
T |
4: 137,016,594 (GRCm39) |
R83W |
probably damaging |
Het |
Zfp820 |
T |
C |
17: 22,038,509 (GRCm39) |
D273G |
probably benign |
Het |
Zfp974 |
A |
T |
7: 27,609,510 (GRCm39) |
Y738* |
probably null |
Het |
Zkscan4 |
A |
C |
13: 21,668,081 (GRCm39) |
E177D |
probably benign |
Het |
|
Other mutations in Trim42 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02289:Trim42
|
APN |
9 |
97,241,286 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02987:Trim42
|
APN |
9 |
97,247,868 (GRCm39) |
missense |
probably benign |
0.28 |
R0116:Trim42
|
UTSW |
9 |
97,245,456 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1170:Trim42
|
UTSW |
9 |
97,245,673 (GRCm39) |
missense |
probably benign |
0.04 |
R1397:Trim42
|
UTSW |
9 |
97,247,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R1499:Trim42
|
UTSW |
9 |
97,248,138 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1522:Trim42
|
UTSW |
9 |
97,247,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R2094:Trim42
|
UTSW |
9 |
97,248,150 (GRCm39) |
missense |
probably benign |
0.23 |
R2355:Trim42
|
UTSW |
9 |
97,241,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R4621:Trim42
|
UTSW |
9 |
97,245,201 (GRCm39) |
missense |
probably benign |
|
R4649:Trim42
|
UTSW |
9 |
97,244,998 (GRCm39) |
missense |
probably benign |
0.00 |
R4840:Trim42
|
UTSW |
9 |
97,244,982 (GRCm39) |
missense |
probably benign |
0.02 |
R6147:Trim42
|
UTSW |
9 |
97,245,382 (GRCm39) |
missense |
probably benign |
|
R7048:Trim42
|
UTSW |
9 |
97,245,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R7235:Trim42
|
UTSW |
9 |
97,251,761 (GRCm39) |
missense |
probably damaging |
0.99 |
R7276:Trim42
|
UTSW |
9 |
97,251,625 (GRCm39) |
nonsense |
probably null |
|
R7390:Trim42
|
UTSW |
9 |
97,241,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R7442:Trim42
|
UTSW |
9 |
97,244,998 (GRCm39) |
missense |
probably damaging |
0.97 |
R7650:Trim42
|
UTSW |
9 |
97,245,201 (GRCm39) |
missense |
probably benign |
|
R7881:Trim42
|
UTSW |
9 |
97,245,070 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8060:Trim42
|
UTSW |
9 |
97,245,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R8427:Trim42
|
UTSW |
9 |
97,245,174 (GRCm39) |
missense |
probably benign |
0.25 |
R8751:Trim42
|
UTSW |
9 |
97,251,852 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8850:Trim42
|
UTSW |
9 |
97,248,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R8856:Trim42
|
UTSW |
9 |
97,245,275 (GRCm39) |
nonsense |
probably null |
|
R8941:Trim42
|
UTSW |
9 |
97,245,100 (GRCm39) |
missense |
probably benign |
0.00 |
R9329:Trim42
|
UTSW |
9 |
97,251,584 (GRCm39) |
missense |
probably benign |
0.37 |
R9427:Trim42
|
UTSW |
9 |
97,247,874 (GRCm39) |
missense |
probably damaging |
0.99 |
R9792:Trim42
|
UTSW |
9 |
97,245,429 (GRCm39) |
missense |
probably damaging |
1.00 |
R9793:Trim42
|
UTSW |
9 |
97,245,429 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Trim42
|
UTSW |
9 |
97,251,675 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Trim42
|
UTSW |
9 |
97,244,959 (GRCm39) |
missense |
probably damaging |
1.00 |
|