Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actr3b |
A |
G |
5: 26,054,895 (GRCm39) |
Y403C |
probably benign |
Het |
Afdn |
A |
G |
17: 14,066,562 (GRCm39) |
I600V |
probably benign |
Het |
Akr1b8 |
G |
A |
6: 34,333,278 (GRCm39) |
E52K |
possibly damaging |
Het |
Alas1 |
A |
G |
9: 106,113,842 (GRCm39) |
S468P |
probably damaging |
Het |
Atp13a5 |
T |
C |
16: 29,133,491 (GRCm39) |
T432A |
probably benign |
Het |
B3glct |
A |
T |
5: 149,650,304 (GRCm39) |
T136S |
probably benign |
Het |
Bahcc1 |
A |
T |
11: 120,159,147 (GRCm39) |
R125* |
probably null |
Het |
Brat1 |
A |
G |
5: 140,704,273 (GRCm39) |
E842G |
probably damaging |
Het |
Cacna1b |
A |
G |
2: 24,508,287 (GRCm39) |
L1830S |
probably damaging |
Het |
Cd109 |
A |
G |
9: 78,579,217 (GRCm39) |
N620D |
probably benign |
Het |
Cdhr1 |
T |
A |
14: 36,803,462 (GRCm39) |
D538V |
probably damaging |
Het |
Cfap74 |
G |
A |
4: 155,514,402 (GRCm39) |
C546Y |
|
Het |
Colq |
T |
A |
14: 31,250,777 (GRCm39) |
R343* |
probably null |
Het |
Dmxl2 |
T |
C |
9: 54,358,187 (GRCm39) |
K330R |
probably benign |
Het |
Dnah5 |
A |
G |
15: 28,233,316 (GRCm39) |
K225R |
probably benign |
Het |
Fyco1 |
C |
A |
9: 123,626,761 (GRCm39) |
A1317S |
probably benign |
Het |
Gm9195 |
G |
A |
14: 72,687,705 (GRCm39) |
P1944L |
probably damaging |
Het |
Gse1 |
T |
G |
8: 121,215,864 (GRCm39) |
L4R |
probably damaging |
Het |
Gstm1 |
T |
C |
3: 107,925,080 (GRCm39) |
I4M |
probably benign |
Het |
Ighv2-3 |
A |
T |
12: 113,574,945 (GRCm39) |
I70K |
possibly damaging |
Het |
Krt71 |
C |
T |
15: 101,645,069 (GRCm39) |
R414H |
probably damaging |
Het |
Mcmbp |
T |
C |
7: 128,317,696 (GRCm39) |
E183G |
possibly damaging |
Het |
Med13l |
T |
C |
5: 118,880,144 (GRCm39) |
S1079P |
probably damaging |
Het |
Megf11 |
A |
G |
9: 64,545,591 (GRCm39) |
I125V |
possibly damaging |
Het |
Mtmr4 |
T |
A |
11: 87,494,962 (GRCm39) |
V418E |
probably damaging |
Het |
Mttp |
T |
C |
3: 137,814,725 (GRCm39) |
T517A |
probably damaging |
Het |
Mx1 |
A |
G |
16: 97,252,893 (GRCm39) |
V409A |
probably benign |
Het |
Olfml1 |
C |
A |
7: 107,167,069 (GRCm39) |
H33N |
probably benign |
Het |
Or13p8 |
A |
C |
4: 118,584,079 (GRCm39) |
I212L |
probably benign |
Het |
Or4k15b |
A |
T |
14: 50,272,224 (GRCm39) |
V212D |
probably benign |
Het |
Or5w19 |
A |
T |
2: 87,698,478 (GRCm39) |
I48F |
possibly damaging |
Het |
Or6k2 |
T |
C |
1: 173,986,417 (GRCm39) |
I26T |
probably benign |
Het |
Or6n1 |
T |
A |
1: 173,917,356 (GRCm39) |
I250N |
possibly damaging |
Het |
Parp12 |
C |
A |
6: 39,067,185 (GRCm39) |
V536F |
probably damaging |
Het |
Phf11a |
T |
C |
14: 59,514,862 (GRCm39) |
E273G |
possibly damaging |
Het |
Pramel27 |
A |
G |
4: 143,579,818 (GRCm39) |
T468A |
possibly damaging |
Het |
Psd3 |
A |
G |
8: 68,210,778 (GRCm39) |
Y743H |
probably damaging |
Het |
Rnf213 |
T |
A |
11: 119,333,365 (GRCm39) |
I2859N |
|
Het |
Sec23a |
A |
T |
12: 59,052,060 (GRCm39) |
C88* |
probably null |
Het |
Sepsecs |
A |
G |
5: 52,826,239 (GRCm39) |
|
probably null |
Het |
Slc35e3 |
G |
A |
10: 117,572,016 (GRCm39) |
T293I |
probably benign |
Het |
Slc49a3 |
G |
T |
5: 108,593,403 (GRCm39) |
T145N |
probably benign |
Het |
Smu1 |
A |
G |
4: 40,739,538 (GRCm39) |
I424T |
possibly damaging |
Het |
Spata16 |
T |
A |
3: 26,968,925 (GRCm39) |
I435N |
probably damaging |
Het |
Tasp1 |
A |
G |
2: 139,838,015 (GRCm39) |
S156P |
probably benign |
Het |
Tmem237 |
A |
C |
1: 59,144,735 (GRCm39) |
S398A |
probably damaging |
Het |
Ttc39c |
T |
A |
18: 12,828,542 (GRCm39) |
L234Q |
probably damaging |
Het |
Ubxn11 |
C |
A |
4: 133,851,426 (GRCm39) |
T22K |
probably benign |
Het |
Uts2r |
C |
A |
11: 121,051,518 (GRCm39) |
S127R |
probably damaging |
Het |
Vmn1r236 |
A |
G |
17: 21,506,969 (GRCm39) |
D29G |
probably benign |
Het |
Vmn2r87 |
A |
G |
10: 130,308,138 (GRCm39) |
I700T |
probably damaging |
Het |
Vmn2r87 |
T |
A |
10: 130,312,064 (GRCm39) |
T517S |
probably benign |
Het |
Vps13b |
T |
A |
15: 35,675,022 (GRCm39) |
V1714E |
probably damaging |
Het |
Wrn |
T |
A |
8: 33,758,950 (GRCm39) |
I1003L |
probably benign |
Het |
Ylpm1 |
A |
G |
12: 85,077,109 (GRCm39) |
D1278G |
possibly damaging |
Het |
Zfp1006 |
T |
A |
8: 129,946,534 (GRCm39) |
H97L |
probably benign |
Het |
Zfp955a |
A |
C |
17: 33,461,888 (GRCm39) |
H81Q |
possibly damaging |
Het |
Zfyve26 |
T |
C |
12: 79,293,006 (GRCm39) |
T2048A |
probably damaging |
Het |
|
Other mutations in Dnase1l3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03349:Dnase1l3
|
APN |
14 |
7,984,146 (GRCm38) |
missense |
probably benign |
0.28 |
R0668:Dnase1l3
|
UTSW |
14 |
7,968,086 (GRCm38) |
critical splice donor site |
probably null |
|
R1282:Dnase1l3
|
UTSW |
14 |
7,983,117 (GRCm38) |
missense |
probably benign |
0.16 |
R1460:Dnase1l3
|
UTSW |
14 |
7,974,050 (GRCm38) |
missense |
probably benign |
0.10 |
R1768:Dnase1l3
|
UTSW |
14 |
7,974,104 (GRCm38) |
missense |
probably damaging |
1.00 |
R2418:Dnase1l3
|
UTSW |
14 |
7,968,089 (GRCm38) |
missense |
possibly damaging |
0.89 |
R5175:Dnase1l3
|
UTSW |
14 |
7,987,386 (GRCm38) |
nonsense |
probably null |
|
R5271:Dnase1l3
|
UTSW |
14 |
7,993,843 (GRCm38) |
missense |
probably damaging |
1.00 |
R5508:Dnase1l3
|
UTSW |
14 |
7,968,146 (GRCm38) |
missense |
probably damaging |
1.00 |
R5561:Dnase1l3
|
UTSW |
14 |
7,967,847 (GRCm38) |
missense |
probably damaging |
1.00 |
R6374:Dnase1l3
|
UTSW |
14 |
7,974,115 (GRCm38) |
missense |
probably damaging |
1.00 |
R7734:Dnase1l3
|
UTSW |
14 |
7,977,144 (GRCm38) |
missense |
probably benign |
0.04 |
R8165:Dnase1l3
|
UTSW |
14 |
7,994,299 (GRCm38) |
start gained |
probably benign |
|
R8421:Dnase1l3
|
UTSW |
14 |
7,968,122 (GRCm38) |
missense |
possibly damaging |
0.94 |
R9094:Dnase1l3
|
UTSW |
14 |
7,987,306 (GRCm38) |
missense |
probably damaging |
1.00 |
R9586:Dnase1l3
|
UTSW |
14 |
7,967,796 (GRCm38) |
missense |
possibly damaging |
0.52 |
|