Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm2 |
T |
A |
4: 144,282,303 (GRCm39) |
H163L |
probably benign |
Het |
Abca13 |
T |
A |
11: 9,242,886 (GRCm39) |
V1583E |
possibly damaging |
Het |
Ablim1 |
G |
T |
19: 57,031,463 (GRCm39) |
S654Y |
probably damaging |
Het |
Acbd4 |
T |
C |
11: 102,994,819 (GRCm39) |
F59S |
probably damaging |
Het |
Acot1 |
T |
C |
12: 84,063,708 (GRCm39) |
I272T |
probably damaging |
Het |
Ankhd1 |
A |
G |
18: 36,773,409 (GRCm39) |
D1402G |
probably damaging |
Het |
Birc6 |
T |
A |
17: 74,945,371 (GRCm39) |
F2800I |
possibly damaging |
Het |
Brd1 |
T |
C |
15: 88,585,401 (GRCm39) |
E811G |
probably benign |
Het |
Catspere2 |
C |
T |
1: 177,874,555 (GRCm39) |
P141S |
unknown |
Het |
Ccdc106 |
A |
G |
7: 5,059,220 (GRCm39) |
|
probably null |
Het |
Ccdc81 |
G |
T |
7: 89,542,324 (GRCm39) |
A184E |
possibly damaging |
Het |
Cenpt |
T |
C |
8: 106,573,000 (GRCm39) |
T364A |
probably benign |
Het |
Crybg2 |
T |
C |
4: 133,808,505 (GRCm39) |
S1060P |
probably damaging |
Het |
Dnttip2 |
A |
G |
3: 122,069,111 (GRCm39) |
T109A |
possibly damaging |
Het |
Dpy19l2 |
A |
G |
9: 24,607,089 (GRCm39) |
L124P |
probably benign |
Het |
Eif1ad19 |
A |
T |
12: 87,740,283 (GRCm39) |
I92N |
probably damaging |
Het |
Fat3 |
T |
C |
9: 15,849,501 (GRCm39) |
D3967G |
probably benign |
Het |
Fbxo21 |
T |
A |
5: 118,146,208 (GRCm39) |
F610L |
probably benign |
Het |
Fmo9 |
T |
C |
1: 166,494,878 (GRCm39) |
D341G |
probably benign |
Het |
Frem3 |
A |
T |
8: 81,342,507 (GRCm39) |
H1600L |
possibly damaging |
Het |
Fry |
A |
T |
5: 150,263,892 (GRCm39) |
K133N |
possibly damaging |
Het |
Gm10647 |
A |
G |
9: 66,705,612 (GRCm39) |
|
probably benign |
Het |
Gmps |
T |
C |
3: 63,906,119 (GRCm39) |
F472S |
probably benign |
Het |
Grb10 |
T |
C |
11: 11,884,192 (GRCm39) |
|
probably benign |
Het |
Grm6 |
G |
A |
11: 50,750,792 (GRCm39) |
G652S |
probably damaging |
Het |
Heca |
G |
T |
10: 17,783,848 (GRCm39) |
D468E |
probably damaging |
Het |
Heg1 |
C |
T |
16: 33,583,985 (GRCm39) |
S1033L |
probably damaging |
Het |
Hepacam2 |
A |
G |
6: 3,487,094 (GRCm39) |
S12P |
probably damaging |
Het |
Impdh1 |
G |
T |
6: 29,206,325 (GRCm39) |
H195N |
probably benign |
Het |
Ipo7 |
T |
C |
7: 109,649,972 (GRCm39) |
|
probably benign |
Het |
Itpr2 |
C |
T |
6: 146,251,520 (GRCm39) |
|
probably null |
Het |
Kcnh6 |
G |
A |
11: 105,899,848 (GRCm39) |
C39Y |
probably benign |
Het |
Kif26a |
T |
C |
12: 112,143,837 (GRCm39) |
S1364P |
probably damaging |
Het |
Lins1 |
T |
A |
7: 66,361,796 (GRCm39) |
|
probably benign |
Het |
Lrpap1 |
C |
T |
5: 35,252,232 (GRCm39) |
V328M |
possibly damaging |
Het |
Lyn |
T |
G |
4: 3,748,768 (GRCm39) |
L249V |
probably benign |
Het |
Mpp7 |
A |
G |
18: 7,439,555 (GRCm39) |
|
probably benign |
Het |
Mtmr9 |
A |
G |
14: 63,765,696 (GRCm39) |
F400L |
possibly damaging |
Het |
Mto1 |
G |
A |
9: 78,381,154 (GRCm39) |
S666N |
probably benign |
Het |
Nanos3 |
C |
T |
8: 84,902,763 (GRCm39) |
R133Q |
probably damaging |
Het |
Nsg1 |
T |
C |
5: 38,312,974 (GRCm39) |
E75G |
probably benign |
Het |
Nsun4 |
A |
G |
4: 115,892,970 (GRCm39) |
M283T |
probably benign |
Het |
Obscn |
A |
G |
11: 58,890,888 (GRCm39) |
S7215P |
unknown |
Het |
Or11j4 |
T |
C |
14: 50,630,321 (GRCm39) |
I36T |
probably benign |
Het |
Or13a20 |
T |
C |
7: 140,232,224 (GRCm39) |
S111P |
probably damaging |
Het |
Or1j12 |
G |
A |
2: 36,343,107 (GRCm39) |
R170K |
probably benign |
Het |
Or2y13 |
G |
A |
11: 49,415,033 (GRCm39) |
S161N |
possibly damaging |
Het |
Or52e4 |
T |
A |
7: 104,706,297 (GRCm39) |
Y281* |
probably null |
Het |
Or5al1 |
A |
C |
2: 85,989,918 (GRCm39) |
S265R |
possibly damaging |
Het |
Or9m1b |
T |
C |
2: 87,836,331 (GRCm39) |
I264V |
probably damaging |
Het |
Per1 |
T |
C |
11: 68,994,869 (GRCm39) |
F563S |
probably benign |
Het |
Pik3c3 |
T |
A |
18: 30,436,131 (GRCm39) |
|
probably benign |
Het |
Pitrm1 |
A |
T |
13: 6,605,675 (GRCm39) |
K207N |
probably damaging |
Het |
Prdm10 |
C |
T |
9: 31,227,526 (GRCm39) |
R44C |
probably damaging |
Het |
Rab40c |
A |
T |
17: 26,104,122 (GRCm39) |
I90N |
probably damaging |
Het |
Rbl1 |
A |
G |
2: 157,041,334 (GRCm39) |
|
probably null |
Het |
Rnf17 |
G |
A |
14: 56,751,563 (GRCm39) |
G1467E |
probably damaging |
Het |
Rpgrip1 |
A |
G |
14: 52,386,841 (GRCm39) |
|
probably benign |
Het |
Sall1 |
A |
T |
8: 89,756,896 (GRCm39) |
N1069K |
probably benign |
Het |
Scap |
T |
C |
9: 110,201,290 (GRCm39) |
I93T |
possibly damaging |
Het |
Sez6 |
T |
C |
11: 77,865,170 (GRCm39) |
|
probably benign |
Het |
Slc22a30 |
A |
T |
19: 8,347,561 (GRCm39) |
S280T |
probably benign |
Het |
Slc26a5 |
A |
C |
5: 22,016,342 (GRCm39) |
|
probably null |
Het |
St18 |
T |
C |
1: 6,919,172 (GRCm39) |
V901A |
probably benign |
Het |
Syne2 |
T |
C |
12: 76,010,650 (GRCm39) |
L2519P |
probably damaging |
Het |
Syne4 |
G |
A |
7: 30,018,344 (GRCm39) |
G362E |
probably damaging |
Het |
Tmem51 |
T |
C |
4: 141,759,236 (GRCm39) |
T171A |
probably benign |
Het |
Tns4 |
A |
T |
11: 98,966,024 (GRCm39) |
I453N |
probably damaging |
Het |
Trank1 |
A |
T |
9: 111,221,978 (GRCm39) |
H2905L |
probably benign |
Het |
Trim13 |
C |
T |
14: 61,842,166 (GRCm39) |
T61I |
possibly damaging |
Het |
Ttn |
C |
A |
2: 76,559,544 (GRCm39) |
R29619L |
probably damaging |
Het |
Ugt2b38 |
T |
A |
5: 87,568,417 (GRCm39) |
M293L |
probably benign |
Het |
Vmn1r22 |
T |
A |
6: 57,877,513 (GRCm39) |
N155Y |
probably benign |
Het |
Vmn2r18 |
T |
C |
5: 151,508,269 (GRCm39) |
Y285C |
probably benign |
Het |
Vmn2r84 |
C |
T |
10: 130,222,588 (GRCm39) |
|
probably benign |
Het |
Vwde |
A |
C |
6: 13,220,004 (GRCm39) |
L49R |
probably damaging |
Het |
Yipf2 |
T |
A |
9: 21,503,262 (GRCm39) |
E68D |
possibly damaging |
Het |
Zfand5 |
C |
A |
19: 21,257,122 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Trim75 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01337:Trim75
|
APN |
8 |
65,436,387 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL02959:Trim75
|
APN |
8 |
65,435,417 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL03026:Trim75
|
APN |
8 |
65,436,438 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03155:Trim75
|
APN |
8 |
65,435,992 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL03228:Trim75
|
APN |
8 |
65,436,006 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03241:Trim75
|
APN |
8 |
65,435,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R0413:Trim75
|
UTSW |
8 |
65,435,892 (GRCm39) |
missense |
probably benign |
0.26 |
R0523:Trim75
|
UTSW |
8 |
65,436,442 (GRCm39) |
missense |
probably benign |
0.05 |
R1675:Trim75
|
UTSW |
8 |
65,435,163 (GRCm39) |
missense |
probably damaging |
0.99 |
R1721:Trim75
|
UTSW |
8 |
65,435,391 (GRCm39) |
splice site |
probably null |
|
R3861:Trim75
|
UTSW |
8 |
65,435,479 (GRCm39) |
missense |
probably damaging |
1.00 |
R4196:Trim75
|
UTSW |
8 |
65,435,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R4469:Trim75
|
UTSW |
8 |
65,436,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R4740:Trim75
|
UTSW |
8 |
65,435,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R5049:Trim75
|
UTSW |
8 |
65,435,091 (GRCm39) |
splice site |
probably null |
|
R6046:Trim75
|
UTSW |
8 |
65,435,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R6227:Trim75
|
UTSW |
8 |
65,435,748 (GRCm39) |
missense |
probably benign |
0.30 |
R6254:Trim75
|
UTSW |
8 |
65,436,094 (GRCm39) |
nonsense |
probably null |
|
R6444:Trim75
|
UTSW |
8 |
65,435,488 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7363:Trim75
|
UTSW |
8 |
65,435,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R7936:Trim75
|
UTSW |
8 |
65,435,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R9328:Trim75
|
UTSW |
8 |
65,435,315 (GRCm39) |
missense |
probably benign |
0.06 |
R9453:Trim75
|
UTSW |
8 |
65,436,561 (GRCm39) |
start gained |
probably benign |
|
X0019:Trim75
|
UTSW |
8 |
65,436,183 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Trim75
|
UTSW |
8 |
65,435,593 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1177:Trim75
|
UTSW |
8 |
65,435,313 (GRCm39) |
missense |
probably damaging |
1.00 |
|