Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921509C19Rik |
A |
G |
2: 151,315,489 (GRCm39) |
L63P |
possibly damaging |
Het |
Abca13 |
A |
T |
11: 9,479,010 (GRCm39) |
Y4286F |
probably benign |
Het |
Aldh5a1 |
A |
C |
13: 25,095,572 (GRCm39) |
V515G |
possibly damaging |
Het |
Ankrd42 |
T |
C |
7: 92,241,141 (GRCm39) |
E406G |
possibly damaging |
Het |
Arfgef2 |
T |
A |
2: 166,707,733 (GRCm39) |
M1043K |
probably benign |
Het |
Arhgef11 |
T |
A |
3: 87,616,879 (GRCm39) |
Y383* |
probably null |
Het |
Aste1 |
C |
T |
9: 105,282,335 (GRCm39) |
P614L |
probably damaging |
Het |
B3galt5 |
T |
A |
16: 96,117,005 (GRCm39) |
S213T |
probably damaging |
Het |
Bak1 |
A |
G |
17: 27,241,434 (GRCm39) |
L108P |
possibly damaging |
Het |
Bcl6 |
G |
A |
16: 23,784,976 (GRCm39) |
R675* |
probably null |
Het |
Bdp1 |
T |
G |
13: 100,197,659 (GRCm39) |
T909P |
possibly damaging |
Het |
Cacna1i |
A |
G |
15: 80,279,439 (GRCm39) |
H2060R |
probably benign |
Het |
Cdhr3 |
G |
T |
12: 33,111,772 (GRCm39) |
P246Q |
probably damaging |
Het |
Colgalt1 |
T |
C |
8: 72,076,354 (GRCm39) |
S602P |
probably damaging |
Het |
Csde1 |
T |
C |
3: 102,947,269 (GRCm39) |
S74P |
probably damaging |
Het |
Cyp51 |
A |
T |
5: 4,137,846 (GRCm39) |
C366S |
possibly damaging |
Het |
Dcaf7 |
A |
G |
11: 105,928,016 (GRCm39) |
N23D |
probably damaging |
Het |
Ddx10 |
G |
A |
9: 53,028,588 (GRCm39) |
A772V |
probably benign |
Het |
Ddx4 |
A |
G |
13: 112,750,319 (GRCm39) |
F404S |
probably benign |
Het |
Dlg4 |
T |
A |
11: 69,908,042 (GRCm39) |
M1K |
probably null |
Het |
Dnajc6 |
T |
C |
4: 101,470,142 (GRCm39) |
V293A |
probably damaging |
Het |
Etl4 |
G |
T |
2: 20,811,742 (GRCm39) |
R1643L |
probably damaging |
Het |
F13b |
G |
A |
1: 139,435,895 (GRCm39) |
E234K |
probably damaging |
Het |
Fam171a1 |
T |
C |
2: 3,226,766 (GRCm39) |
I633T |
probably benign |
Het |
Frem3 |
A |
G |
8: 81,342,668 (GRCm39) |
I1654V |
probably benign |
Het |
Galr2 |
A |
G |
11: 116,174,408 (GRCm39) |
E346G |
possibly damaging |
Het |
Gck |
G |
A |
11: 5,899,705 (GRCm39) |
|
probably benign |
Het |
Gen1 |
G |
T |
12: 11,291,833 (GRCm39) |
T717K |
probably benign |
Het |
Gpatch8 |
TTCCTCCTCCTCCTCTTCCTCCTCCTC |
TTCCTCCTCCTCCTCCTCTTCCTCCTCCTC |
11: 102,371,014 (GRCm39) |
|
probably benign |
Het |
Hat1 |
A |
G |
2: 71,251,595 (GRCm39) |
T215A |
possibly damaging |
Het |
Hmbox1 |
A |
T |
14: 65,134,486 (GRCm39) |
M38K |
probably damaging |
Het |
Ifi47 |
A |
G |
11: 48,987,369 (GRCm39) |
K379E |
probably benign |
Het |
Ift81 |
T |
C |
5: 122,707,062 (GRCm39) |
Y460C |
probably damaging |
Het |
Jarid2 |
T |
A |
13: 45,055,938 (GRCm39) |
S381R |
probably damaging |
Het |
Kmt2b |
A |
T |
7: 30,279,388 (GRCm39) |
V1458E |
probably damaging |
Het |
Kpna4 |
G |
T |
3: 68,997,266 (GRCm39) |
P336Q |
probably damaging |
Het |
Krt84 |
T |
C |
15: 101,440,689 (GRCm39) |
R168G |
probably damaging |
Het |
Lhx8 |
T |
A |
3: 154,030,221 (GRCm39) |
Y137F |
possibly damaging |
Het |
Lin7b |
T |
C |
7: 45,019,651 (GRCm39) |
E19G |
probably damaging |
Het |
Lrmda |
A |
T |
14: 22,634,608 (GRCm39) |
R131S |
probably damaging |
Het |
Lrrc75b |
C |
T |
10: 75,389,512 (GRCm39) |
A280T |
possibly damaging |
Het |
Megf11 |
G |
A |
9: 64,555,233 (GRCm39) |
R268K |
probably null |
Het |
Mgat4e |
G |
T |
1: 134,469,697 (GRCm39) |
Q116K |
probably damaging |
Het |
Mlkl |
A |
G |
8: 112,046,035 (GRCm39) |
L325P |
probably damaging |
Het |
Mup2 |
A |
G |
4: 60,137,641 (GRCm39) |
L134P |
probably damaging |
Het |
Myo19 |
A |
G |
11: 84,791,412 (GRCm39) |
E489G |
probably damaging |
Het |
Ncbp3 |
C |
A |
11: 72,938,835 (GRCm39) |
P37Q |
probably damaging |
Het |
Nf2 |
A |
G |
11: 4,749,964 (GRCm39) |
V236A |
probably damaging |
Het |
Nlrp1a |
A |
T |
11: 71,014,905 (GRCm39) |
M115K |
possibly damaging |
Het |
Nsf |
T |
A |
11: 103,719,356 (GRCm39) |
K649* |
probably null |
Het |
Olfml2b |
A |
T |
1: 170,494,354 (GRCm39) |
I313L |
probably benign |
Het |
Or2ak4 |
T |
A |
11: 58,649,109 (GRCm39) |
I206N |
probably damaging |
Het |
Or52u1 |
T |
A |
7: 104,237,764 (GRCm39) |
V251D |
possibly damaging |
Het |
Papln |
T |
A |
12: 83,823,295 (GRCm39) |
L444Q |
probably damaging |
Het |
Phc3 |
T |
C |
3: 30,968,346 (GRCm39) |
I897V |
probably benign |
Het |
Plcg1 |
T |
C |
2: 160,596,300 (GRCm39) |
L632P |
probably damaging |
Het |
Pramel21 |
A |
T |
4: 143,342,735 (GRCm39) |
I281F |
probably benign |
Het |
Prkg1 |
T |
C |
19: 31,279,701 (GRCm39) |
T178A |
probably damaging |
Het |
Ptges |
T |
A |
2: 30,782,816 (GRCm39) |
T79S |
probably benign |
Het |
Rab26 |
T |
C |
17: 24,751,263 (GRCm39) |
T81A |
probably damaging |
Het |
Rai14 |
T |
A |
15: 10,595,089 (GRCm39) |
I145L |
possibly damaging |
Het |
Rfx1 |
A |
T |
8: 84,821,455 (GRCm39) |
I755F |
probably damaging |
Het |
Rims1 |
T |
G |
1: 22,503,174 (GRCm39) |
L670F |
probably damaging |
Het |
Rtkn |
G |
A |
6: 83,126,692 (GRCm39) |
C297Y |
probably damaging |
Het |
Sec23a |
A |
T |
12: 59,036,229 (GRCm39) |
N378K |
probably benign |
Het |
Slc1a2 |
T |
C |
2: 102,597,340 (GRCm39) |
M449T |
probably damaging |
Het |
Slc22a3 |
G |
A |
17: 12,652,518 (GRCm39) |
L369F |
possibly damaging |
Het |
Slc34a1 |
A |
G |
13: 24,006,390 (GRCm39) |
E472G |
probably benign |
Het |
Slc49a4 |
G |
T |
16: 35,555,947 (GRCm39) |
T171K |
probably benign |
Het |
Smad6 |
G |
T |
9: 63,929,069 (GRCm39) |
D82E |
unknown |
Het |
Smgc |
A |
T |
15: 91,736,811 (GRCm39) |
I463F |
possibly damaging |
Het |
Strada |
C |
A |
11: 106,061,865 (GRCm39) |
G166C |
probably damaging |
Het |
Tcaf3 |
A |
G |
6: 42,570,825 (GRCm39) |
V309A |
probably benign |
Het |
Tet2 |
C |
T |
3: 133,175,352 (GRCm39) |
E1332K |
possibly damaging |
Het |
Tfcp2l1 |
A |
G |
1: 118,596,362 (GRCm39) |
N366D |
probably damaging |
Het |
Tll2 |
G |
A |
19: 41,105,723 (GRCm39) |
P369L |
possibly damaging |
Het |
Tox4 |
T |
C |
14: 52,529,554 (GRCm39) |
V505A |
probably benign |
Het |
Trbv4 |
A |
G |
6: 41,036,787 (GRCm39) |
D104G |
probably damaging |
Het |
Ugdh |
T |
C |
5: 65,574,380 (GRCm39) |
E416G |
probably damaging |
Het |
Usp47 |
T |
A |
7: 111,686,220 (GRCm39) |
C613S |
probably damaging |
Het |
Vmn1r11 |
T |
A |
6: 57,115,147 (GRCm39) |
N270K |
probably benign |
Het |
Wsb2 |
T |
A |
5: 117,509,160 (GRCm39) |
L147Q |
probably damaging |
Het |
Xrn1 |
G |
A |
9: 95,861,198 (GRCm39) |
A453T |
possibly damaging |
Het |
Zan |
A |
G |
5: 137,460,106 (GRCm39) |
S1262P |
unknown |
Het |
Zswim4 |
A |
G |
8: 84,946,556 (GRCm39) |
L700P |
probably damaging |
Het |
|
Other mutations in Rasgrf1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00517:Rasgrf1
|
APN |
9 |
89,852,534 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00763:Rasgrf1
|
APN |
9 |
89,853,073 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01336:Rasgrf1
|
APN |
9 |
89,873,583 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01710:Rasgrf1
|
APN |
9 |
89,873,745 (GRCm39) |
missense |
probably benign |
0.18 |
IGL01807:Rasgrf1
|
APN |
9 |
89,873,566 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01939:Rasgrf1
|
APN |
9 |
89,856,889 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02453:Rasgrf1
|
APN |
9 |
89,826,813 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL02961:Rasgrf1
|
APN |
9 |
89,863,702 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL03009:Rasgrf1
|
APN |
9 |
89,873,756 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL03369:Rasgrf1
|
APN |
9 |
89,892,504 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03373:Rasgrf1
|
APN |
9 |
89,899,084 (GRCm39) |
splice site |
probably benign |
|
Malenkiy
|
UTSW |
9 |
89,892,537 (GRCm39) |
splice site |
probably null |
|
Pigeon
|
UTSW |
9 |
89,849,968 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4142001:Rasgrf1
|
UTSW |
9 |
89,797,626 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0234:Rasgrf1
|
UTSW |
9 |
89,891,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R0629:Rasgrf1
|
UTSW |
9 |
89,866,322 (GRCm39) |
missense |
probably damaging |
1.00 |
R0685:Rasgrf1
|
UTSW |
9 |
89,797,535 (GRCm39) |
utr 3 prime |
probably benign |
|
R0730:Rasgrf1
|
UTSW |
9 |
89,833,062 (GRCm39) |
splice site |
probably benign |
|
R0835:Rasgrf1
|
UTSW |
9 |
89,882,824 (GRCm39) |
missense |
probably benign |
|
R1432:Rasgrf1
|
UTSW |
9 |
89,894,853 (GRCm39) |
missense |
probably benign |
0.35 |
R1647:Rasgrf1
|
UTSW |
9 |
89,835,973 (GRCm39) |
missense |
probably benign |
0.28 |
R1717:Rasgrf1
|
UTSW |
9 |
89,835,966 (GRCm39) |
missense |
probably damaging |
0.98 |
R1933:Rasgrf1
|
UTSW |
9 |
89,835,966 (GRCm39) |
missense |
probably damaging |
0.98 |
R1934:Rasgrf1
|
UTSW |
9 |
89,835,966 (GRCm39) |
missense |
probably damaging |
0.98 |
R2187:Rasgrf1
|
UTSW |
9 |
89,876,888 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2240:Rasgrf1
|
UTSW |
9 |
89,858,815 (GRCm39) |
missense |
probably damaging |
0.99 |
R2940:Rasgrf1
|
UTSW |
9 |
89,873,767 (GRCm39) |
missense |
possibly damaging |
0.84 |
R3949:Rasgrf1
|
UTSW |
9 |
89,863,797 (GRCm39) |
splice site |
probably benign |
|
R4751:Rasgrf1
|
UTSW |
9 |
89,894,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R4751:Rasgrf1
|
UTSW |
9 |
89,792,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R4901:Rasgrf1
|
UTSW |
9 |
89,877,056 (GRCm39) |
missense |
probably benign |
0.00 |
R4910:Rasgrf1
|
UTSW |
9 |
89,858,805 (GRCm39) |
missense |
probably benign |
0.00 |
R4961:Rasgrf1
|
UTSW |
9 |
89,826,922 (GRCm39) |
missense |
probably benign |
0.06 |
R5270:Rasgrf1
|
UTSW |
9 |
89,908,747 (GRCm39) |
missense |
probably benign |
0.00 |
R5320:Rasgrf1
|
UTSW |
9 |
89,902,478 (GRCm39) |
missense |
probably damaging |
0.99 |
R5602:Rasgrf1
|
UTSW |
9 |
89,793,624 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5659:Rasgrf1
|
UTSW |
9 |
89,866,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R5960:Rasgrf1
|
UTSW |
9 |
89,903,437 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6074:Rasgrf1
|
UTSW |
9 |
89,835,968 (GRCm39) |
missense |
probably benign |
0.01 |
R6400:Rasgrf1
|
UTSW |
9 |
89,873,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R6596:Rasgrf1
|
UTSW |
9 |
89,894,847 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6603:Rasgrf1
|
UTSW |
9 |
89,792,310 (GRCm39) |
missense |
probably damaging |
0.96 |
R6647:Rasgrf1
|
UTSW |
9 |
89,892,516 (GRCm39) |
missense |
probably benign |
0.00 |
R6813:Rasgrf1
|
UTSW |
9 |
89,892,537 (GRCm39) |
splice site |
probably null |
|
R7136:Rasgrf1
|
UTSW |
9 |
89,873,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R7175:Rasgrf1
|
UTSW |
9 |
89,862,802 (GRCm39) |
missense |
probably benign |
0.02 |
R7202:Rasgrf1
|
UTSW |
9 |
89,899,125 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7219:Rasgrf1
|
UTSW |
9 |
89,866,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R7244:Rasgrf1
|
UTSW |
9 |
89,876,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R7733:Rasgrf1
|
UTSW |
9 |
89,863,780 (GRCm39) |
missense |
probably benign |
0.01 |
R7764:Rasgrf1
|
UTSW |
9 |
89,876,747 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8210:Rasgrf1
|
UTSW |
9 |
89,793,675 (GRCm39) |
missense |
unknown |
|
R8421:Rasgrf1
|
UTSW |
9 |
89,849,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R8524:Rasgrf1
|
UTSW |
9 |
89,797,638 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8526:Rasgrf1
|
UTSW |
9 |
89,856,901 (GRCm39) |
missense |
probably damaging |
0.96 |
R8697:Rasgrf1
|
UTSW |
9 |
89,877,055 (GRCm39) |
missense |
probably benign |
|
R9133:Rasgrf1
|
UTSW |
9 |
89,793,600 (GRCm39) |
missense |
probably benign |
|
R9153:Rasgrf1
|
UTSW |
9 |
89,826,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R9191:Rasgrf1
|
UTSW |
9 |
89,883,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R9349:Rasgrf1
|
UTSW |
9 |
89,884,460 (GRCm39) |
missense |
probably damaging |
0.99 |
R9468:Rasgrf1
|
UTSW |
9 |
89,880,756 (GRCm39) |
missense |
probably benign |
0.00 |
R9498:Rasgrf1
|
UTSW |
9 |
89,826,921 (GRCm39) |
missense |
probably benign |
|
R9747:Rasgrf1
|
UTSW |
9 |
89,877,047 (GRCm39) |
missense |
probably benign |
|
R9779:Rasgrf1
|
UTSW |
9 |
89,873,551 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Rasgrf1
|
UTSW |
9 |
89,832,970 (GRCm39) |
missense |
probably damaging |
1.00 |
|