Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6430548M08Rik |
A |
T |
8: 120,878,115 (GRCm39) |
H190L |
possibly damaging |
Het |
Adap1 |
A |
G |
5: 139,278,976 (GRCm39) |
|
probably benign |
Het |
Adgra3 |
C |
T |
5: 50,121,182 (GRCm39) |
|
probably benign |
Het |
Adgre5 |
A |
T |
8: 84,451,527 (GRCm39) |
V527E |
probably damaging |
Het |
Anapc5 |
A |
T |
5: 122,938,695 (GRCm39) |
Y360N |
probably damaging |
Het |
Angptl6 |
C |
A |
9: 20,789,683 (GRCm39) |
A70S |
probably benign |
Het |
Ankdd1a |
C |
A |
9: 65,417,610 (GRCm39) |
K137N |
probably null |
Het |
Ccdc170 |
T |
C |
10: 4,496,950 (GRCm39) |
|
probably benign |
Het |
Ccdc51 |
A |
G |
9: 108,920,698 (GRCm39) |
E195G |
probably damaging |
Het |
Cdc37 |
A |
T |
9: 21,053,426 (GRCm39) |
C204S |
possibly damaging |
Het |
Cfap36 |
T |
C |
11: 29,172,431 (GRCm39) |
|
probably benign |
Het |
Col6a2 |
C |
A |
10: 76,432,259 (GRCm39) |
G965C |
probably damaging |
Het |
Csn1s2a |
G |
A |
5: 87,926,826 (GRCm39) |
S53N |
possibly damaging |
Het |
Dab2ip |
T |
C |
2: 35,582,388 (GRCm39) |
|
probably null |
Het |
Dhx58 |
A |
G |
11: 100,587,823 (GRCm39) |
V578A |
probably damaging |
Het |
Diaph1 |
G |
T |
18: 38,024,902 (GRCm39) |
Q520K |
unknown |
Het |
Eefsec |
C |
A |
6: 88,274,631 (GRCm39) |
K444N |
probably benign |
Het |
Eftud2 |
A |
T |
11: 102,759,443 (GRCm39) |
H153Q |
possibly damaging |
Het |
Eif5b |
T |
G |
1: 38,058,324 (GRCm39) |
S209A |
probably benign |
Het |
Exosc2 |
T |
A |
2: 31,562,497 (GRCm39) |
Y46N |
probably damaging |
Het |
F2 |
C |
T |
2: 91,456,075 (GRCm39) |
G562D |
probably damaging |
Het |
Fgf23 |
G |
A |
6: 127,057,128 (GRCm39) |
G148D |
probably damaging |
Het |
Fmnl3 |
G |
C |
15: 99,220,619 (GRCm39) |
|
probably benign |
Het |
Fstl5 |
G |
A |
3: 76,614,786 (GRCm39) |
G179R |
probably damaging |
Het |
Garre1 |
A |
T |
7: 33,938,644 (GRCm39) |
W246R |
probably damaging |
Het |
Gart |
T |
A |
16: 91,422,282 (GRCm39) |
Q745L |
probably benign |
Het |
Gmeb1 |
T |
A |
4: 131,959,419 (GRCm39) |
M212L |
probably benign |
Het |
Gpaa1 |
T |
C |
15: 76,218,981 (GRCm39) |
Y548H |
probably damaging |
Het |
Gpatch1 |
T |
C |
7: 34,986,667 (GRCm39) |
E763G |
probably damaging |
Het |
Grm8 |
T |
A |
6: 27,762,389 (GRCm39) |
I279F |
probably damaging |
Het |
Hcls1 |
T |
A |
16: 36,771,536 (GRCm39) |
H147Q |
probably damaging |
Het |
Hpcal1 |
A |
C |
12: 17,836,389 (GRCm39) |
D73A |
probably damaging |
Het |
Il22ra1 |
T |
C |
4: 135,478,317 (GRCm39) |
S463P |
probably benign |
Het |
Itgbl1 |
G |
A |
14: 124,078,098 (GRCm39) |
|
probably null |
Het |
Izumo3 |
G |
T |
4: 92,035,437 (GRCm39) |
|
probably benign |
Het |
Kcna5 |
A |
T |
6: 126,510,346 (GRCm39) |
L594Q |
probably damaging |
Het |
Kif13a |
A |
T |
13: 46,918,079 (GRCm39) |
D409E |
probably benign |
Het |
Kif9 |
A |
T |
9: 110,314,106 (GRCm39) |
I39F |
probably damaging |
Het |
Klri2 |
C |
T |
6: 129,709,171 (GRCm39) |
R227H |
possibly damaging |
Het |
Lamc3 |
G |
A |
2: 31,798,628 (GRCm39) |
G445S |
probably damaging |
Het |
Lctl |
A |
G |
9: 64,024,980 (GRCm39) |
|
probably benign |
Het |
Lrp4 |
T |
C |
2: 91,325,327 (GRCm39) |
L1384P |
probably damaging |
Het |
Mcm9 |
G |
A |
10: 53,439,526 (GRCm39) |
S549L |
possibly damaging |
Het |
Ms4a15 |
G |
A |
19: 10,956,697 (GRCm39) |
|
probably benign |
Het |
Mtor |
T |
C |
4: 148,555,081 (GRCm39) |
V901A |
possibly damaging |
Het |
Nckap1l |
A |
T |
15: 103,390,391 (GRCm39) |
I721F |
probably benign |
Het |
Nemp2 |
T |
C |
1: 52,684,588 (GRCm39) |
V298A |
probably benign |
Het |
Npc1l1 |
T |
A |
11: 6,178,148 (GRCm39) |
K421* |
probably null |
Het |
Npr1 |
C |
T |
3: 90,363,244 (GRCm39) |
V879M |
probably damaging |
Het |
Odad4 |
A |
G |
11: 100,454,394 (GRCm39) |
E393G |
probably damaging |
Het |
Or2ad1 |
A |
G |
13: 21,326,336 (GRCm39) |
V297A |
possibly damaging |
Het |
Or51q1c |
A |
G |
7: 103,652,709 (GRCm39) |
T82A |
probably benign |
Het |
Osgin1 |
A |
T |
8: 120,169,219 (GRCm39) |
I39F |
possibly damaging |
Het |
Phip |
G |
C |
9: 82,809,244 (GRCm39) |
|
probably null |
Het |
Pkdrej |
G |
T |
15: 85,705,768 (GRCm39) |
P56Q |
possibly damaging |
Het |
Plcxd2 |
A |
G |
16: 45,800,889 (GRCm39) |
Y112H |
probably damaging |
Het |
Plekha1 |
C |
T |
7: 130,499,176 (GRCm39) |
T155M |
probably damaging |
Het |
Prkdc |
T |
C |
16: 15,558,196 (GRCm39) |
|
probably null |
Het |
Prss1 |
A |
G |
6: 41,439,495 (GRCm39) |
H76R |
probably damaging |
Het |
Psg23 |
T |
C |
7: 18,348,558 (GRCm39) |
D83G |
probably benign |
Het |
Ptprd |
T |
A |
4: 76,055,140 (GRCm39) |
Q196L |
probably benign |
Het |
Ranbp3l |
A |
T |
15: 9,063,067 (GRCm39) |
H292L |
probably damaging |
Het |
Ranbp6 |
T |
C |
19: 29,787,097 (GRCm39) |
E1085G |
probably benign |
Het |
Rccd1 |
A |
G |
7: 79,970,326 (GRCm39) |
V97A |
possibly damaging |
Het |
Rchy1 |
T |
C |
5: 92,105,458 (GRCm39) |
S48G |
probably benign |
Het |
Robo3 |
A |
T |
9: 37,336,640 (GRCm39) |
M376K |
probably benign |
Het |
Rrp12 |
T |
C |
19: 41,862,289 (GRCm39) |
D898G |
probably benign |
Het |
Scg3 |
A |
T |
9: 75,570,462 (GRCm39) |
|
probably benign |
Het |
Sec31b |
A |
T |
19: 44,522,821 (GRCm39) |
M57K |
probably damaging |
Het |
Slc17a6 |
A |
C |
7: 51,315,892 (GRCm39) |
I387L |
probably benign |
Het |
Speer4a1 |
T |
A |
5: 26,240,982 (GRCm39) |
Q170L |
possibly damaging |
Het |
Srsf9 |
A |
G |
5: 115,470,260 (GRCm39) |
D146G |
possibly damaging |
Het |
Ss18 |
A |
G |
18: 14,788,200 (GRCm39) |
M90T |
probably damaging |
Het |
Syna |
A |
T |
5: 134,588,314 (GRCm39) |
F212I |
possibly damaging |
Het |
Tex54 |
A |
G |
19: 8,718,221 (GRCm39) |
|
probably benign |
Het |
Thsd1 |
A |
G |
8: 22,733,055 (GRCm39) |
H34R |
probably damaging |
Het |
Tmem143 |
T |
C |
7: 45,547,086 (GRCm39) |
I84T |
probably benign |
Het |
Trim50 |
T |
C |
5: 135,395,487 (GRCm39) |
V281A |
probably damaging |
Het |
Trp53i11 |
C |
A |
2: 93,029,696 (GRCm39) |
|
probably benign |
Het |
Ttll4 |
C |
T |
1: 74,718,851 (GRCm39) |
T234I |
possibly damaging |
Het |
Ttyh1 |
A |
T |
7: 4,127,719 (GRCm39) |
I136F |
possibly damaging |
Het |
Ube2f |
T |
C |
1: 91,189,976 (GRCm39) |
|
probably benign |
Het |
Vcl |
T |
A |
14: 21,037,083 (GRCm39) |
L227* |
probably null |
Het |
Vmn1r222 |
A |
C |
13: 23,416,974 (GRCm39) |
C80G |
probably damaging |
Het |
Vps13b |
G |
T |
15: 35,926,365 (GRCm39) |
A3889S |
probably benign |
Het |
Vps8 |
T |
C |
16: 21,323,136 (GRCm39) |
|
probably benign |
Het |
Zbtb44 |
A |
G |
9: 30,978,006 (GRCm39) |
Y422C |
probably damaging |
Het |
Zfp180 |
A |
G |
7: 23,805,158 (GRCm39) |
S526G |
possibly damaging |
Het |
Zfp518a |
A |
C |
19: 40,904,310 (GRCm39) |
E1413A |
probably damaging |
Het |
Zfp629 |
T |
A |
7: 127,210,858 (GRCm39) |
Y317F |
probably damaging |
Het |
Zfp804b |
T |
C |
5: 6,820,534 (GRCm39) |
E843G |
probably benign |
Het |
|
Other mutations in Rnmt |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02231:Rnmt
|
APN |
18 |
68,447,152 (GRCm39) |
nonsense |
probably null |
|
acre
|
UTSW |
18 |
68,447,105 (GRCm39) |
missense |
probably damaging |
1.00 |
talenti
|
UTSW |
18 |
68,452,285 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03098:Rnmt
|
UTSW |
18 |
68,439,073 (GRCm39) |
missense |
probably damaging |
0.98 |
R0712:Rnmt
|
UTSW |
18 |
68,440,859 (GRCm39) |
critical splice donor site |
probably null |
|
R1493:Rnmt
|
UTSW |
18 |
68,446,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R1541:Rnmt
|
UTSW |
18 |
68,440,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R1606:Rnmt
|
UTSW |
18 |
68,444,724 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2224:Rnmt
|
UTSW |
18 |
68,438,854 (GRCm39) |
start gained |
probably benign |
|
R3114:Rnmt
|
UTSW |
18 |
68,447,079 (GRCm39) |
missense |
probably benign |
0.13 |
R3115:Rnmt
|
UTSW |
18 |
68,447,079 (GRCm39) |
missense |
probably benign |
0.13 |
R4424:Rnmt
|
UTSW |
18 |
68,444,742 (GRCm39) |
missense |
probably null |
0.07 |
R4705:Rnmt
|
UTSW |
18 |
68,447,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R4722:Rnmt
|
UTSW |
18 |
68,438,952 (GRCm39) |
missense |
probably damaging |
0.98 |
R4732:Rnmt
|
UTSW |
18 |
68,451,031 (GRCm39) |
intron |
probably benign |
|
R5173:Rnmt
|
UTSW |
18 |
68,454,430 (GRCm39) |
utr 3 prime |
probably benign |
|
R5523:Rnmt
|
UTSW |
18 |
68,446,773 (GRCm39) |
missense |
probably benign |
|
R5579:Rnmt
|
UTSW |
18 |
68,439,186 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5966:Rnmt
|
UTSW |
18 |
68,444,689 (GRCm39) |
missense |
probably benign |
0.16 |
R6322:Rnmt
|
UTSW |
18 |
68,452,285 (GRCm39) |
missense |
probably damaging |
0.98 |
R7149:Rnmt
|
UTSW |
18 |
68,452,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R7529:Rnmt
|
UTSW |
18 |
68,444,726 (GRCm39) |
missense |
probably benign |
0.41 |
R7620:Rnmt
|
UTSW |
18 |
68,447,105 (GRCm39) |
missense |
probably damaging |
1.00 |
R8071:Rnmt
|
UTSW |
18 |
68,440,723 (GRCm39) |
missense |
probably benign |
0.03 |
R9093:Rnmt
|
UTSW |
18 |
68,451,146 (GRCm39) |
missense |
probably benign |
0.03 |
R9436:Rnmt
|
UTSW |
18 |
68,442,410 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1088:Rnmt
|
UTSW |
18 |
68,440,745 (GRCm39) |
missense |
probably benign |
0.14 |
|