Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6820408C15Rik |
C |
G |
2: 152,282,777 (GRCm39) |
P211A |
probably damaging |
Het |
Ambra1 |
G |
A |
2: 91,715,951 (GRCm39) |
V761M |
probably damaging |
Het |
Amfr |
T |
A |
8: 94,702,798 (GRCm39) |
|
probably null |
Het |
Asphd1 |
C |
A |
7: 126,545,287 (GRCm39) |
A357S |
probably benign |
Het |
Brd3 |
C |
A |
2: 27,353,931 (GRCm39) |
Q60H |
probably damaging |
Het |
Cd96 |
T |
A |
16: 45,890,016 (GRCm39) |
M336L |
probably benign |
Het |
Cep152 |
T |
A |
2: 125,406,125 (GRCm39) |
H1469L |
probably benign |
Het |
Coro1a |
G |
T |
7: 126,299,816 (GRCm39) |
|
probably null |
Het |
D630045J12Rik |
A |
T |
6: 38,171,555 (GRCm39) |
L871Q |
probably benign |
Het |
Depdc5 |
C |
T |
5: 33,095,635 (GRCm39) |
P824L |
probably damaging |
Het |
Enpep |
T |
G |
3: 129,099,075 (GRCm39) |
D467A |
probably damaging |
Het |
Extl2 |
G |
A |
3: 115,821,013 (GRCm39) |
A273T |
probably benign |
Het |
Foxi3 |
T |
A |
6: 70,937,500 (GRCm39) |
F218Y |
probably damaging |
Het |
Golga2 |
A |
G |
2: 32,194,166 (GRCm39) |
M521V |
probably benign |
Het |
Gpr142 |
T |
A |
11: 114,695,168 (GRCm39) |
N44K |
probably damaging |
Het |
Gtf2ird2 |
A |
G |
5: 134,245,061 (GRCm39) |
I440V |
probably benign |
Het |
Gucy1b2 |
T |
A |
14: 62,642,028 (GRCm39) |
K698I |
probably damaging |
Het |
Hspa1b |
T |
C |
17: 35,177,983 (GRCm39) |
M1V |
probably null |
Het |
Ints9 |
T |
A |
14: 65,245,521 (GRCm39) |
Y260N |
probably benign |
Het |
Khdc3 |
T |
G |
9: 73,010,768 (GRCm39) |
V182G |
possibly damaging |
Het |
Ky |
A |
G |
9: 102,414,798 (GRCm39) |
|
probably null |
Het |
Map2k1 |
T |
A |
9: 64,098,843 (GRCm39) |
I263F |
probably damaging |
Het |
Or13a18 |
A |
C |
7: 140,190,576 (GRCm39) |
I166L |
probably benign |
Het |
Or2t47 |
T |
C |
11: 58,442,877 (GRCm39) |
S63G |
probably benign |
Het |
Or5ak25 |
A |
G |
2: 85,269,241 (GRCm39) |
V87A |
probably benign |
Het |
Otogl |
T |
A |
10: 107,613,453 (GRCm39) |
H2004L |
probably benign |
Het |
Palmd |
T |
C |
3: 116,717,009 (GRCm39) |
H496R |
probably benign |
Het |
Papolb |
C |
G |
5: 142,515,409 (GRCm39) |
R78P |
possibly damaging |
Het |
Pcdh10 |
G |
A |
3: 45,336,247 (GRCm39) |
G854R |
probably damaging |
Het |
Pdcd11 |
A |
G |
19: 47,101,976 (GRCm39) |
I1054V |
probably benign |
Het |
Pik3ap1 |
A |
T |
19: 41,364,545 (GRCm39) |
L58Q |
probably damaging |
Het |
Ppp2ca |
A |
G |
11: 51,989,937 (GRCm39) |
K21R |
probably benign |
Het |
Prmt5 |
A |
C |
14: 54,745,373 (GRCm39) |
I598S |
probably damaging |
Het |
Pycr1 |
T |
A |
11: 120,532,050 (GRCm39) |
I239F |
probably damaging |
Het |
R3hdm2 |
C |
T |
10: 127,334,285 (GRCm39) |
R896C |
probably damaging |
Het |
Rev3l |
C |
T |
10: 39,722,725 (GRCm39) |
P699S |
probably damaging |
Het |
Samd1 |
CGAGGAGGAGGAGGAGGAGGA |
CGAGGAGGAGGAGGAGGA |
8: 84,725,625 (GRCm39) |
|
probably benign |
Het |
Sel1l |
A |
T |
12: 91,791,658 (GRCm39) |
M351K |
possibly damaging |
Het |
Sesn2 |
A |
G |
4: 132,226,617 (GRCm39) |
L159P |
probably damaging |
Het |
Slc35f4 |
T |
A |
14: 49,540,946 (GRCm39) |
|
probably benign |
Het |
Slc3a1 |
C |
A |
17: 85,359,403 (GRCm39) |
N409K |
probably damaging |
Het |
Slc45a2 |
C |
T |
15: 11,027,871 (GRCm39) |
T480I |
probably damaging |
Het |
Slco1c1 |
T |
C |
6: 141,492,502 (GRCm39) |
F246S |
probably damaging |
Het |
Socs2 |
T |
G |
10: 95,228,681 (GRCm39) |
I190L |
unknown |
Het |
Srsf1 |
T |
A |
11: 87,938,684 (GRCm39) |
I7N |
possibly damaging |
Het |
Stox1 |
T |
A |
10: 62,503,620 (GRCm39) |
H145L |
probably damaging |
Het |
Trap1 |
A |
T |
16: 3,874,286 (GRCm39) |
I243N |
probably damaging |
Het |
Trav7-3 |
T |
C |
14: 53,681,207 (GRCm39) |
I83T |
probably benign |
Het |
Tuft1 |
A |
T |
3: 94,546,712 (GRCm39) |
I42K |
possibly damaging |
Het |
Umps |
A |
G |
16: 33,787,344 (GRCm39) |
V3A |
probably benign |
Het |
Vim |
A |
C |
2: 13,579,643 (GRCm39) |
E134A |
probably null |
Het |
Vmn1r28 |
C |
A |
6: 58,242,524 (GRCm39) |
H122Q |
probably benign |
Het |
Vps51 |
T |
G |
19: 6,121,063 (GRCm39) |
E283D |
probably benign |
Het |
Vsig10l |
T |
A |
7: 43,120,274 (GRCm39) |
V760D |
probably damaging |
Het |
Xrn1 |
A |
G |
9: 95,927,596 (GRCm39) |
D1460G |
probably benign |
Het |
Zfp282 |
A |
G |
6: 47,874,824 (GRCm39) |
D343G |
probably damaging |
Het |
Zfp35 |
A |
G |
18: 24,136,778 (GRCm39) |
H374R |
probably damaging |
Het |
|
Other mutations in Trmt9b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00518:Trmt9b
|
APN |
8 |
36,979,453 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01360:Trmt9b
|
APN |
8 |
36,979,713 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01364:Trmt9b
|
APN |
8 |
36,979,501 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03401:Trmt9b
|
APN |
8 |
36,972,823 (GRCm39) |
missense |
probably damaging |
1.00 |
Bear_market
|
UTSW |
8 |
36,965,637 (GRCm39) |
critical splice donor site |
probably null |
|
R2161:Trmt9b
|
UTSW |
8 |
36,972,804 (GRCm39) |
missense |
probably damaging |
1.00 |
R2230:Trmt9b
|
UTSW |
8 |
36,979,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R2232:Trmt9b
|
UTSW |
8 |
36,979,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R4250:Trmt9b
|
UTSW |
8 |
36,979,366 (GRCm39) |
missense |
probably benign |
0.05 |
R4432:Trmt9b
|
UTSW |
8 |
36,965,632 (GRCm39) |
missense |
probably damaging |
1.00 |
R4491:Trmt9b
|
UTSW |
8 |
36,972,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R5242:Trmt9b
|
UTSW |
8 |
36,979,084 (GRCm39) |
missense |
probably benign |
0.02 |
R5482:Trmt9b
|
UTSW |
8 |
36,979,203 (GRCm39) |
missense |
probably benign |
|
R5579:Trmt9b
|
UTSW |
8 |
36,979,195 (GRCm39) |
missense |
probably benign |
0.00 |
R5594:Trmt9b
|
UTSW |
8 |
36,979,452 (GRCm39) |
missense |
probably benign |
0.00 |
R5797:Trmt9b
|
UTSW |
8 |
36,965,569 (GRCm39) |
nonsense |
probably null |
|
R6481:Trmt9b
|
UTSW |
8 |
36,965,637 (GRCm39) |
critical splice donor site |
probably null |
|
R7504:Trmt9b
|
UTSW |
8 |
36,979,309 (GRCm39) |
missense |
probably benign |
0.03 |
R8119:Trmt9b
|
UTSW |
8 |
36,965,576 (GRCm39) |
nonsense |
probably null |
|
R8169:Trmt9b
|
UTSW |
8 |
36,978,857 (GRCm39) |
missense |
probably damaging |
0.97 |
R8962:Trmt9b
|
UTSW |
8 |
36,972,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R9034:Trmt9b
|
UTSW |
8 |
36,978,954 (GRCm39) |
nonsense |
probably null |
|
R9035:Trmt9b
|
UTSW |
8 |
36,978,954 (GRCm39) |
nonsense |
probably null |
|
R9647:Trmt9b
|
UTSW |
8 |
36,979,210 (GRCm39) |
missense |
probably benign |
0.00 |
X0057:Trmt9b
|
UTSW |
8 |
36,979,142 (GRCm39) |
nonsense |
probably null |
|
X0065:Trmt9b
|
UTSW |
8 |
36,979,010 (GRCm39) |
missense |
possibly damaging |
0.71 |
|