Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acss3 |
T |
G |
10: 106,889,313 (GRCm39) |
Y169S |
probably damaging |
Het |
Apc2 |
A |
G |
10: 80,141,378 (GRCm39) |
K268E |
probably damaging |
Het |
Arhgef2 |
G |
C |
3: 88,551,185 (GRCm39) |
R765P |
probably benign |
Het |
Bptf |
T |
C |
11: 106,972,349 (GRCm39) |
K840E |
probably damaging |
Het |
Carf |
A |
G |
1: 60,175,506 (GRCm39) |
R245G |
possibly damaging |
Het |
Cd36 |
A |
G |
5: 17,990,718 (GRCm39) |
|
probably null |
Het |
Cep250 |
G |
A |
2: 155,834,552 (GRCm39) |
R2159K |
probably damaging |
Het |
Cldn34c4 |
A |
T |
X: 126,629,011 (GRCm39) |
V153E |
probably damaging |
Het |
Col4a4 |
T |
A |
1: 82,501,643 (GRCm39) |
Y370F |
unknown |
Het |
Cplane1 |
T |
A |
15: 8,241,842 (GRCm39) |
|
probably null |
Het |
Ddx4 |
A |
G |
13: 112,750,295 (GRCm39) |
V386A |
probably benign |
Het |
Exoc6 |
A |
G |
19: 37,560,360 (GRCm39) |
T126A |
probably benign |
Het |
Fam83f |
A |
T |
15: 80,576,393 (GRCm39) |
N348I |
possibly damaging |
Het |
Gja8 |
A |
G |
3: 96,826,468 (GRCm39) |
V398A |
probably benign |
Het |
Gkn3 |
C |
T |
6: 87,360,507 (GRCm39) |
A163T |
probably damaging |
Het |
Gm12789 |
A |
T |
4: 101,845,526 (GRCm39) |
T72S |
possibly damaging |
Het |
Gm1988 |
A |
G |
7: 38,820,292 (GRCm39) |
|
noncoding transcript |
Het |
Gm21370 |
A |
G |
13: 120,488,489 (GRCm39) |
V20A |
probably benign |
Het |
Hjurp |
G |
C |
1: 88,204,937 (GRCm39) |
|
probably benign |
Het |
Hsd17b13 |
T |
A |
5: 104,113,720 (GRCm39) |
S245C |
probably benign |
Het |
Htr1f |
T |
C |
16: 64,746,324 (GRCm39) |
K323E |
probably benign |
Het |
Igkc |
T |
C |
6: 70,703,442 (GRCm39) |
|
probably benign |
Het |
Ksr1 |
T |
C |
11: 78,918,303 (GRCm39) |
E535G |
probably damaging |
Het |
Mlxipl |
A |
T |
5: 135,161,381 (GRCm39) |
E433D |
probably benign |
Het |
Npc1 |
T |
C |
18: 12,331,219 (GRCm39) |
|
probably null |
Het |
Or10ak7 |
C |
T |
4: 118,791,230 (GRCm39) |
E272K |
probably benign |
Het |
Or1e29 |
A |
G |
11: 73,667,667 (GRCm39) |
L162P |
probably damaging |
Het |
Or6y1 |
A |
G |
1: 174,276,500 (GRCm39) |
T104A |
probably benign |
Het |
Or7g17 |
T |
C |
9: 18,768,398 (GRCm39) |
I159T |
probably benign |
Het |
Pcdha3 |
A |
G |
18: 37,081,504 (GRCm39) |
R749G |
probably benign |
Het |
Ppme1 |
A |
T |
7: 99,997,044 (GRCm39) |
N122K |
possibly damaging |
Het |
Rasal1 |
G |
A |
5: 120,813,674 (GRCm39) |
V657M |
possibly damaging |
Het |
Rbm47 |
A |
G |
5: 66,180,080 (GRCm39) |
M409T |
probably benign |
Het |
Rragd |
C |
T |
4: 33,007,155 (GRCm39) |
T161M |
probably damaging |
Het |
Slurp1 |
T |
C |
15: 74,598,724 (GRCm39) |
H89R |
possibly damaging |
Het |
Snap23 |
A |
G |
2: 120,416,061 (GRCm39) |
I42V |
probably benign |
Het |
Sypl2 |
A |
G |
3: 108,124,992 (GRCm39) |
I123T |
possibly damaging |
Het |
Taar8a |
T |
A |
10: 23,953,062 (GRCm39) |
V222E |
probably damaging |
Het |
Tmem171 |
A |
T |
13: 98,829,096 (GRCm39) |
V18D |
probably damaging |
Het |
Topors |
T |
C |
4: 40,260,794 (GRCm39) |
D830G |
unknown |
Het |
Traf3ip3 |
A |
G |
1: 192,863,628 (GRCm39) |
V414A |
probably damaging |
Het |
Tubg1 |
T |
A |
11: 101,015,364 (GRCm39) |
M270K |
possibly damaging |
Het |
Vmn1r188 |
T |
C |
13: 22,272,772 (GRCm39) |
V242A |
probably benign |
Het |
Vmn1r19 |
T |
A |
6: 57,381,720 (GRCm39) |
I91N |
probably damaging |
Het |
Vmn2r12 |
T |
A |
5: 109,239,412 (GRCm39) |
M384L |
probably benign |
Het |
Wdr26 |
T |
C |
1: 181,030,679 (GRCm39) |
E205G |
probably damaging |
Het |
Zfp281 |
T |
A |
1: 136,553,859 (GRCm39) |
I279N |
probably damaging |
Het |
Zfp398 |
T |
A |
6: 47,843,159 (GRCm39) |
C272S |
probably damaging |
Het |
|
Other mutations in Zfp975 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02008:Zfp975
|
APN |
7 |
42,312,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R0194:Zfp975
|
UTSW |
7 |
42,311,916 (GRCm39) |
missense |
probably benign |
0.02 |
R0662:Zfp975
|
UTSW |
7 |
42,311,950 (GRCm39) |
missense |
probably benign |
0.02 |
R1491:Zfp975
|
UTSW |
7 |
42,312,236 (GRCm39) |
missense |
probably benign |
0.19 |
R1573:Zfp975
|
UTSW |
7 |
42,311,507 (GRCm39) |
missense |
probably benign |
0.03 |
R1738:Zfp975
|
UTSW |
7 |
42,312,373 (GRCm39) |
missense |
probably benign |
0.05 |
R1833:Zfp975
|
UTSW |
7 |
42,311,263 (GRCm39) |
missense |
probably benign |
0.01 |
R2185:Zfp975
|
UTSW |
7 |
42,311,105 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4031:Zfp975
|
UTSW |
7 |
42,312,377 (GRCm39) |
nonsense |
probably null |
|
R4356:Zfp975
|
UTSW |
7 |
42,311,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R4631:Zfp975
|
UTSW |
7 |
42,312,369 (GRCm39) |
missense |
probably benign |
0.09 |
R4795:Zfp975
|
UTSW |
7 |
42,314,570 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4896:Zfp975
|
UTSW |
7 |
42,311,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R5266:Zfp975
|
UTSW |
7 |
42,311,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R5267:Zfp975
|
UTSW |
7 |
42,311,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R5580:Zfp975
|
UTSW |
7 |
42,314,513 (GRCm39) |
nonsense |
probably null |
|
R5874:Zfp975
|
UTSW |
7 |
42,312,312 (GRCm39) |
missense |
probably benign |
0.00 |
R5898:Zfp975
|
UTSW |
7 |
42,311,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R6529:Zfp975
|
UTSW |
7 |
42,311,325 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6782:Zfp975
|
UTSW |
7 |
42,311,454 (GRCm39) |
missense |
probably benign |
0.41 |
R6937:Zfp975
|
UTSW |
7 |
42,314,480 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7088:Zfp975
|
UTSW |
7 |
42,312,096 (GRCm39) |
missense |
probably benign |
0.02 |
R7233:Zfp975
|
UTSW |
7 |
42,311,918 (GRCm39) |
missense |
probably benign |
0.38 |
R7253:Zfp975
|
UTSW |
7 |
42,311,036 (GRCm39) |
makesense |
probably null |
|
R7358:Zfp975
|
UTSW |
7 |
42,312,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R7659:Zfp975
|
UTSW |
7 |
42,311,848 (GRCm39) |
missense |
probably benign |
0.00 |
R7999:Zfp975
|
UTSW |
7 |
42,312,356 (GRCm39) |
missense |
probably benign |
0.02 |
R8676:Zfp975
|
UTSW |
7 |
42,312,264 (GRCm39) |
missense |
probably benign |
0.44 |
R8957:Zfp975
|
UTSW |
7 |
42,311,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R9274:Zfp975
|
UTSW |
7 |
42,312,299 (GRCm39) |
missense |
probably benign |
0.02 |
R9326:Zfp975
|
UTSW |
7 |
42,311,837 (GRCm39) |
nonsense |
probably null |
|
R9536:Zfp975
|
UTSW |
7 |
42,312,345 (GRCm39) |
missense |
probably benign |
0.11 |
R9569:Zfp975
|
UTSW |
7 |
42,311,413 (GRCm39) |
missense |
probably benign |
0.00 |
R9717:Zfp975
|
UTSW |
7 |
42,312,332 (GRCm39) |
missense |
possibly damaging |
0.50 |
|