Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
T |
C |
7: 120,139,320 (GRCm39) |
Y1451H |
probably damaging |
Het |
Abca7 |
T |
A |
10: 79,833,471 (GRCm39) |
M8K |
possibly damaging |
Het |
Ablim3 |
C |
A |
18: 61,972,805 (GRCm39) |
R238L |
probably damaging |
Het |
Adar |
T |
A |
3: 89,658,368 (GRCm39) |
Y1141* |
probably null |
Het |
Arid2 |
T |
C |
15: 96,269,067 (GRCm39) |
I1060T |
probably damaging |
Het |
Armc2 |
A |
T |
10: 41,839,774 (GRCm39) |
V397D |
possibly damaging |
Het |
Astn2 |
A |
G |
4: 66,322,386 (GRCm39) |
V71A |
unknown |
Het |
Bcat2 |
A |
G |
7: 45,234,542 (GRCm39) |
D141G |
probably damaging |
Het |
Bicdl1 |
C |
A |
5: 115,862,769 (GRCm39) |
R162L |
probably damaging |
Het |
Btbd17 |
A |
G |
11: 114,684,910 (GRCm39) |
I43T |
possibly damaging |
Het |
C2cd5 |
A |
T |
6: 142,977,019 (GRCm39) |
C698* |
probably null |
Het |
Calr |
T |
A |
8: 85,572,629 (GRCm39) |
K87* |
probably null |
Het |
Cap2 |
C |
T |
13: 46,768,818 (GRCm39) |
T208I |
probably benign |
Het |
Col14a1 |
A |
T |
15: 55,364,780 (GRCm39) |
M1630L |
probably benign |
Het |
Copg1 |
T |
G |
6: 87,887,072 (GRCm39) |
S816A |
possibly damaging |
Het |
Csf2ra |
C |
A |
19: 61,215,280 (GRCm39) |
A112S |
possibly damaging |
Het |
Cwc27 |
T |
A |
13: 104,933,799 (GRCm39) |
H241L |
probably benign |
Het |
Dgki |
T |
A |
6: 36,892,422 (GRCm39) |
E852V |
probably damaging |
Het |
Dpp6 |
T |
C |
5: 27,868,521 (GRCm39) |
|
probably null |
Het |
Dynlrb1 |
T |
C |
2: 155,089,860 (GRCm39) |
|
probably null |
Het |
Ehhadh |
C |
T |
16: 21,592,281 (GRCm39) |
V141I |
probably benign |
Het |
Esyt3 |
A |
G |
9: 99,194,044 (GRCm39) |
L865P |
probably damaging |
Het |
Fam83h |
T |
A |
15: 75,873,924 (GRCm39) |
T1138S |
possibly damaging |
Het |
Fzd4 |
T |
C |
7: 89,056,912 (GRCm39) |
W320R |
probably damaging |
Het |
Gimap7 |
A |
T |
6: 48,701,260 (GRCm39) |
K282M |
probably benign |
Het |
Gnai2 |
G |
A |
9: 107,492,913 (GRCm39) |
T330I |
|
Het |
Gpr107 |
T |
C |
2: 31,078,728 (GRCm39) |
S388P |
possibly damaging |
Het |
Il1a |
T |
G |
2: 129,142,654 (GRCm39) |
M264L |
probably benign |
Het |
Ints10 |
A |
T |
8: 69,279,951 (GRCm39) |
I693F |
probably damaging |
Het |
Jak3 |
A |
T |
8: 72,134,265 (GRCm39) |
N456Y |
probably benign |
Het |
Krcc1 |
A |
G |
6: 71,261,457 (GRCm39) |
E163G |
probably benign |
Het |
Lctl |
A |
G |
9: 64,040,455 (GRCm39) |
Y466C |
probably damaging |
Het |
Lrp12 |
A |
T |
15: 39,741,357 (GRCm39) |
S472T |
probably damaging |
Het |
Lrp1b |
A |
G |
2: 41,335,111 (GRCm39) |
|
probably null |
Het |
Lrriq1 |
T |
A |
10: 103,057,144 (GRCm39) |
M219L |
probably benign |
Het |
Mbl2 |
T |
A |
19: 30,216,741 (GRCm39) |
D184E |
probably damaging |
Het |
Mrgpra9 |
G |
A |
7: 46,885,392 (GRCm39) |
R92C |
probably benign |
Het |
Mroh4 |
G |
A |
15: 74,483,405 (GRCm39) |
T644I |
probably damaging |
Het |
Muc5ac |
C |
T |
7: 141,369,255 (GRCm39) |
A3114V |
probably benign |
Het |
Myh11 |
T |
A |
16: 14,029,152 (GRCm39) |
M1197L |
|
Het |
Naga |
C |
T |
15: 82,221,084 (GRCm39) |
G71S |
probably damaging |
Het |
Nicn1 |
C |
T |
9: 108,171,708 (GRCm39) |
R163C |
possibly damaging |
Het |
Nos1 |
G |
C |
5: 118,017,402 (GRCm39) |
R255P |
probably benign |
Het |
Nsd3 |
A |
G |
8: 26,199,088 (GRCm39) |
|
probably null |
Het |
Nsun6 |
T |
C |
2: 15,047,048 (GRCm39) |
T101A |
probably benign |
Het |
Or55b10 |
T |
A |
7: 102,144,084 (GRCm39) |
|
probably benign |
Het |
Pabpc4l |
T |
A |
3: 46,401,326 (GRCm39) |
D106V |
probably damaging |
Het |
Pdlim5 |
G |
A |
3: 141,953,109 (GRCm39) |
P529L |
probably damaging |
Het |
Ralgapa1 |
A |
G |
12: 55,755,843 (GRCm39) |
L1111P |
possibly damaging |
Het |
Rangap1 |
T |
C |
15: 81,606,221 (GRCm39) |
D40G |
probably benign |
Het |
Ripor2 |
T |
C |
13: 24,915,663 (GRCm39) |
F1078L |
probably damaging |
Het |
Ryr3 |
T |
C |
2: 112,610,336 (GRCm39) |
D2312G |
probably damaging |
Het |
Siglecg |
T |
A |
7: 43,058,853 (GRCm39) |
I202N |
probably benign |
Het |
Slco4c1 |
G |
T |
1: 96,795,644 (GRCm39) |
S138* |
probably null |
Het |
Snx27 |
T |
C |
3: 94,431,593 (GRCm39) |
Y267C |
probably damaging |
Het |
Sphk2 |
C |
T |
7: 45,361,179 (GRCm39) |
R275H |
probably damaging |
Het |
Stk36 |
T |
A |
1: 74,655,793 (GRCm39) |
V432E |
possibly damaging |
Het |
Tecrl |
C |
T |
5: 83,428,422 (GRCm39) |
S283N |
possibly damaging |
Het |
Tenm2 |
T |
A |
11: 35,914,474 (GRCm39) |
E2354D |
probably damaging |
Het |
Tmem59l |
A |
G |
8: 70,937,822 (GRCm39) |
V186A |
possibly damaging |
Het |
Try4 |
T |
C |
6: 41,282,008 (GRCm39) |
|
probably null |
Het |
Ubr1 |
C |
A |
2: 120,727,000 (GRCm39) |
G1248V |
probably benign |
Het |
Umod |
C |
T |
7: 119,065,355 (GRCm39) |
G558E |
probably damaging |
Het |
Unc13b |
T |
C |
4: 43,171,044 (GRCm39) |
F624S |
unknown |
Het |
Uvssa |
T |
G |
5: 33,547,365 (GRCm39) |
D310E |
probably benign |
Het |
Vmn1r222 |
A |
T |
13: 23,416,418 (GRCm39) |
M265K |
probably benign |
Het |
Vmn1r3 |
A |
G |
4: 3,185,284 (GRCm39) |
F8L |
probably benign |
Het |
Zfp268 |
C |
G |
4: 145,349,156 (GRCm39) |
Q198E |
possibly damaging |
Het |
|
Other mutations in Zfp386 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01982:Zfp386
|
APN |
12 |
116,022,788 (GRCm39) |
missense |
probably benign |
|
IGL02692:Zfp386
|
APN |
12 |
116,022,855 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03071:Zfp386
|
APN |
12 |
116,022,760 (GRCm39) |
missense |
probably benign |
0.08 |
F5493:Zfp386
|
UTSW |
12 |
116,023,922 (GRCm39) |
missense |
probably damaging |
0.99 |
R0098:Zfp386
|
UTSW |
12 |
116,022,834 (GRCm39) |
nonsense |
probably null |
|
R0098:Zfp386
|
UTSW |
12 |
116,022,834 (GRCm39) |
nonsense |
probably null |
|
R0372:Zfp386
|
UTSW |
12 |
116,018,436 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0784:Zfp386
|
UTSW |
12 |
116,023,540 (GRCm39) |
nonsense |
probably null |
|
R0866:Zfp386
|
UTSW |
12 |
116,018,329 (GRCm39) |
splice site |
probably benign |
|
R0947:Zfp386
|
UTSW |
12 |
116,023,398 (GRCm39) |
missense |
probably benign |
0.11 |
R1080:Zfp386
|
UTSW |
12 |
116,023,426 (GRCm39) |
nonsense |
probably null |
|
R1517:Zfp386
|
UTSW |
12 |
116,023,225 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1597:Zfp386
|
UTSW |
12 |
116,023,709 (GRCm39) |
missense |
probably damaging |
0.99 |
R1722:Zfp386
|
UTSW |
12 |
116,023,526 (GRCm39) |
missense |
probably damaging |
0.99 |
R2043:Zfp386
|
UTSW |
12 |
116,022,781 (GRCm39) |
missense |
probably benign |
0.22 |
R3741:Zfp386
|
UTSW |
12 |
116,023,170 (GRCm39) |
nonsense |
probably null |
|
R3742:Zfp386
|
UTSW |
12 |
116,023,170 (GRCm39) |
nonsense |
probably null |
|
R3902:Zfp386
|
UTSW |
12 |
116,023,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R5012:Zfp386
|
UTSW |
12 |
116,022,864 (GRCm39) |
missense |
probably benign |
|
R5590:Zfp386
|
UTSW |
12 |
116,023,347 (GRCm39) |
missense |
probably benign |
0.41 |
R5709:Zfp386
|
UTSW |
12 |
116,023,305 (GRCm39) |
missense |
probably benign |
0.23 |
R6156:Zfp386
|
UTSW |
12 |
116,023,526 (GRCm39) |
missense |
probably damaging |
0.99 |
R6184:Zfp386
|
UTSW |
12 |
116,024,133 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6423:Zfp386
|
UTSW |
12 |
116,023,733 (GRCm39) |
missense |
probably damaging |
0.96 |
R8015:Zfp386
|
UTSW |
12 |
116,023,027 (GRCm39) |
missense |
probably damaging |
0.96 |
R8120:Zfp386
|
UTSW |
12 |
116,018,573 (GRCm39) |
missense |
unknown |
|
R8137:Zfp386
|
UTSW |
12 |
116,023,268 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9093:Zfp386
|
UTSW |
12 |
116,023,878 (GRCm39) |
nonsense |
probably null |
|
R9269:Zfp386
|
UTSW |
12 |
116,023,283 (GRCm39) |
missense |
probably benign |
0.01 |
R9331:Zfp386
|
UTSW |
12 |
116,011,433 (GRCm39) |
start gained |
probably benign |
|
R9536:Zfp386
|
UTSW |
12 |
116,023,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R9641:Zfp386
|
UTSW |
12 |
116,023,330 (GRCm39) |
missense |
probably benign |
0.03 |
Z1088:Zfp386
|
UTSW |
12 |
116,018,393 (GRCm39) |
missense |
possibly damaging |
0.95 |
|