Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrl3 |
T |
C |
5: 81,919,532 (GRCm39) |
|
probably benign |
Het |
Adgrl4 |
A |
G |
3: 151,223,418 (GRCm39) |
I624V |
probably damaging |
Het |
AI661453 |
A |
G |
17: 47,780,287 (GRCm39) |
|
probably benign |
Het |
Alg12 |
C |
T |
15: 88,700,181 (GRCm39) |
E60K |
probably damaging |
Het |
Angel2 |
A |
T |
1: 190,665,284 (GRCm39) |
N72Y |
possibly damaging |
Het |
Ank1 |
C |
A |
8: 23,630,183 (GRCm39) |
P81Q |
probably damaging |
Het |
Atp6v1c2 |
A |
T |
12: 17,371,613 (GRCm39) |
D61E |
probably damaging |
Het |
Bpi |
T |
A |
2: 158,103,254 (GRCm39) |
M83K |
probably damaging |
Het |
Capn7 |
A |
G |
14: 31,090,072 (GRCm39) |
I642V |
probably benign |
Het |
Ccdc134 |
T |
C |
15: 82,015,938 (GRCm39) |
|
probably benign |
Het |
Ccr3 |
C |
T |
9: 123,829,061 (GRCm39) |
T132I |
probably damaging |
Het |
Cfap65 |
C |
A |
1: 74,971,077 (GRCm39) |
W80C |
probably damaging |
Het |
Chaf1a |
T |
A |
17: 56,354,384 (GRCm39) |
I218K |
unknown |
Het |
Ddx23 |
A |
G |
15: 98,554,481 (GRCm39) |
|
probably null |
Het |
Dmkn |
A |
G |
7: 30,464,719 (GRCm39) |
S231G |
probably benign |
Het |
Ep300 |
T |
C |
15: 81,525,514 (GRCm39) |
I1446T |
unknown |
Het |
Fmnl1 |
T |
C |
11: 103,080,795 (GRCm39) |
F318S |
probably damaging |
Het |
Grik5 |
A |
T |
7: 24,722,805 (GRCm39) |
V497E |
probably damaging |
Het |
Gtf2ird2 |
T |
C |
5: 134,242,925 (GRCm39) |
Y380H |
probably damaging |
Het |
Hecw2 |
C |
T |
1: 53,907,990 (GRCm39) |
|
probably benign |
Het |
Hspb7 |
A |
G |
4: 141,151,358 (GRCm39) |
I167V |
probably damaging |
Het |
Kcnh2 |
T |
A |
5: 24,527,700 (GRCm39) |
N884I |
probably benign |
Het |
Krba1 |
T |
C |
6: 48,382,159 (GRCm39) |
|
probably benign |
Het |
Krt18 |
G |
T |
15: 101,939,409 (GRCm39) |
R294L |
probably benign |
Het |
Lctl |
T |
A |
9: 64,029,389 (GRCm39) |
M1K |
probably null |
Het |
Lingo2 |
G |
A |
4: 35,708,375 (GRCm39) |
S535F |
possibly damaging |
Het |
Lrba |
A |
C |
3: 86,449,995 (GRCm39) |
N2105H |
probably damaging |
Het |
Lrrc10 |
A |
G |
10: 116,881,419 (GRCm39) |
D31G |
probably damaging |
Het |
Lrrtm1 |
T |
A |
6: 77,220,855 (GRCm39) |
V104E |
probably damaging |
Het |
Mgat3 |
C |
T |
15: 80,096,778 (GRCm39) |
T535I |
probably benign |
Het |
Nav3 |
T |
C |
10: 109,552,503 (GRCm39) |
I1780V |
possibly damaging |
Het |
Nlrc4 |
A |
G |
17: 74,753,826 (GRCm39) |
W186R |
probably damaging |
Het |
Nr2c1 |
T |
A |
10: 94,024,117 (GRCm39) |
F441I |
probably benign |
Het |
Obscn |
A |
G |
11: 58,942,347 (GRCm39) |
|
probably benign |
Het |
Or1p1 |
T |
C |
11: 74,179,501 (GRCm39) |
F10L |
probably benign |
Het |
Or2a56 |
T |
C |
6: 42,932,707 (GRCm39) |
S92P |
probably benign |
Het |
Or56b34 |
T |
C |
7: 104,937,726 (GRCm39) |
V142A |
probably damaging |
Het |
Or5au1 |
T |
C |
14: 52,273,442 (GRCm39) |
N42S |
possibly damaging |
Het |
Osr1 |
A |
T |
12: 9,629,691 (GRCm39) |
Y188F |
probably damaging |
Het |
Pappa |
A |
T |
4: 65,226,049 (GRCm39) |
T1301S |
probably damaging |
Het |
Pde4dip |
G |
A |
3: 97,660,442 (GRCm39) |
Q679* |
probably null |
Het |
Pik3r5 |
T |
A |
11: 68,377,448 (GRCm39) |
|
probably null |
Het |
Plbd2 |
C |
T |
5: 120,624,104 (GRCm39) |
|
probably null |
Het |
Ppp1r3a |
G |
T |
6: 14,754,516 (GRCm39) |
P244T |
possibly damaging |
Het |
Pum1 |
C |
A |
4: 130,499,985 (GRCm39) |
R960S |
probably benign |
Het |
Ralgapb |
T |
C |
2: 158,315,169 (GRCm39) |
Y845H |
probably damaging |
Het |
Rbms1 |
A |
T |
2: 60,589,179 (GRCm39) |
M287K |
possibly damaging |
Het |
Rdh1 |
A |
T |
10: 127,595,906 (GRCm39) |
I34F |
probably damaging |
Het |
Rgl3 |
T |
A |
9: 21,885,398 (GRCm39) |
Q644L |
probably benign |
Het |
Rpap2 |
T |
C |
5: 107,768,340 (GRCm39) |
S393P |
probably damaging |
Het |
Rsad2 |
T |
C |
12: 26,506,376 (GRCm39) |
S15G |
probably damaging |
Het |
Rspo1 |
G |
A |
4: 124,885,190 (GRCm39) |
R22Q |
probably benign |
Het |
S100a11 |
A |
C |
3: 93,431,509 (GRCm39) |
|
probably null |
Het |
Septin4 |
T |
C |
11: 87,472,022 (GRCm39) |
S11P |
probably benign |
Het |
Serpina1c |
T |
C |
12: 103,862,350 (GRCm39) |
S322G |
probably benign |
Het |
Setdb1 |
A |
T |
3: 95,248,762 (GRCm39) |
C385S |
probably damaging |
Het |
Shank2 |
A |
T |
7: 143,746,204 (GRCm39) |
I193F |
possibly damaging |
Het |
Slc4a11 |
G |
T |
2: 130,528,221 (GRCm39) |
|
probably benign |
Het |
Snrnp40 |
C |
G |
4: 130,271,836 (GRCm39) |
|
probably null |
Het |
Tbcd |
C |
A |
11: 121,485,100 (GRCm39) |
Q761K |
probably benign |
Het |
Tmed6 |
C |
T |
8: 107,792,198 (GRCm39) |
V16M |
probably damaging |
Het |
Tmem229a |
T |
C |
6: 24,955,701 (GRCm39) |
T18A |
probably benign |
Het |
Tsc1 |
T |
A |
2: 28,568,955 (GRCm39) |
|
probably benign |
Het |
Ube2m |
T |
C |
7: 12,769,657 (GRCm39) |
N49D |
probably damaging |
Het |
Ubqlnl |
T |
C |
7: 103,799,254 (GRCm39) |
D81G |
probably damaging |
Het |
Vmn2r56 |
A |
G |
7: 12,449,332 (GRCm39) |
V302A |
probably benign |
Het |
Vmn2r73 |
T |
A |
7: 85,525,075 (GRCm39) |
R24S |
probably benign |
Het |
Wfs1 |
C |
A |
5: 37,130,538 (GRCm39) |
S236I |
probably damaging |
Het |
Xpot |
A |
T |
10: 121,441,544 (GRCm39) |
N560K |
probably benign |
Het |
Yipf3 |
A |
G |
17: 46,562,503 (GRCm39) |
T303A |
probably benign |
Het |
Zfp790 |
T |
C |
7: 29,524,300 (GRCm39) |
W19R |
probably damaging |
Het |
Zfp846 |
T |
C |
9: 20,505,303 (GRCm39) |
C388R |
probably benign |
Het |
Zpr1 |
T |
A |
9: 46,184,634 (GRCm39) |
I47N |
probably damaging |
Het |
|
Other mutations in Pak2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01380:Pak2
|
APN |
16 |
31,860,362 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01807:Pak2
|
APN |
16 |
31,856,097 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02296:Pak2
|
APN |
16 |
31,862,820 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02828:Pak2
|
APN |
16 |
31,840,674 (GRCm39) |
missense |
probably damaging |
1.00 |
K7371:Pak2
|
UTSW |
16 |
31,852,602 (GRCm39) |
splice site |
probably benign |
|
PIT4142001:Pak2
|
UTSW |
16 |
31,841,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R1569:Pak2
|
UTSW |
16 |
31,856,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R4179:Pak2
|
UTSW |
16 |
31,871,005 (GRCm39) |
missense |
probably benign |
0.02 |
R4180:Pak2
|
UTSW |
16 |
31,871,005 (GRCm39) |
missense |
probably benign |
0.02 |
R4223:Pak2
|
UTSW |
16 |
31,871,028 (GRCm39) |
missense |
probably benign |
|
R5114:Pak2
|
UTSW |
16 |
31,861,936 (GRCm39) |
intron |
probably benign |
|
R5294:Pak2
|
UTSW |
16 |
31,840,648 (GRCm39) |
missense |
probably damaging |
0.99 |
R5340:Pak2
|
UTSW |
16 |
31,853,764 (GRCm39) |
splice site |
probably null |
|
R5342:Pak2
|
UTSW |
16 |
31,863,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R5586:Pak2
|
UTSW |
16 |
31,860,337 (GRCm39) |
missense |
probably benign |
0.00 |
R7590:Pak2
|
UTSW |
16 |
31,871,014 (GRCm39) |
missense |
probably benign |
0.27 |
R7995:Pak2
|
UTSW |
16 |
31,846,590 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8324:Pak2
|
UTSW |
16 |
31,871,029 (GRCm39) |
missense |
probably benign |
0.00 |
R8485:Pak2
|
UTSW |
16 |
31,871,083 (GRCm39) |
missense |
probably benign |
0.16 |
R8948:Pak2
|
UTSW |
16 |
31,852,729 (GRCm39) |
splice site |
probably benign |
|
R9723:Pak2
|
UTSW |
16 |
31,852,650 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Pak2
|
UTSW |
16 |
31,863,396 (GRCm39) |
missense |
probably benign |
0.08 |
|