Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
T |
A |
13: 77,415,896 (GRCm39) |
L663Q |
probably damaging |
Het |
2610008E11Rik |
C |
G |
10: 78,903,568 (GRCm39) |
R249S |
probably benign |
Het |
6030469F06Rik |
A |
G |
12: 31,235,058 (GRCm39) |
N146S |
noncoding transcript |
Het |
Abcb5 |
G |
A |
12: 118,838,467 (GRCm39) |
P1032S |
probably benign |
Het |
Acvr2a |
A |
T |
2: 48,789,736 (GRCm39) |
D493V |
possibly damaging |
Het |
Amacr |
A |
G |
15: 10,995,004 (GRCm39) |
D272G |
probably benign |
Het |
Bach1 |
A |
C |
16: 87,526,467 (GRCm39) |
K643T |
probably damaging |
Het |
Bmt2 |
T |
C |
6: 13,628,672 (GRCm39) |
Y337C |
probably damaging |
Het |
Bsn |
A |
G |
9: 107,994,578 (GRCm39) |
S566P |
probably benign |
Het |
Cass4 |
A |
C |
2: 172,269,094 (GRCm39) |
D392A |
probably benign |
Het |
Cbx2 |
A |
G |
11: 118,918,954 (GRCm39) |
E173G |
probably damaging |
Het |
Ccdc166 |
G |
C |
15: 75,852,860 (GRCm39) |
A369G |
probably benign |
Het |
Ccdc77 |
G |
A |
6: 120,308,870 (GRCm39) |
T315M |
possibly damaging |
Het |
Ceacam10 |
C |
A |
7: 24,480,513 (GRCm39) |
H215N |
unknown |
Het |
Ces1e |
C |
T |
8: 93,929,947 (GRCm39) |
M445I |
probably benign |
Het |
Ces2b |
T |
G |
8: 105,563,112 (GRCm39) |
V350G |
possibly damaging |
Het |
Chtf18 |
A |
G |
17: 25,941,165 (GRCm39) |
L611P |
probably benign |
Het |
Col9a1 |
C |
A |
1: 24,217,380 (GRCm39) |
P19T |
unknown |
Het |
Csf1r |
A |
T |
18: 61,250,750 (GRCm39) |
N487I |
probably damaging |
Het |
Csl |
A |
T |
10: 99,594,161 (GRCm39) |
H301Q |
probably damaging |
Het |
Cyp24a1 |
G |
A |
2: 170,332,036 (GRCm39) |
T330M |
probably damaging |
Het |
Ddb2 |
T |
C |
2: 91,042,645 (GRCm39) |
D405G |
probably damaging |
Het |
Degs1 |
A |
G |
1: 182,110,241 (GRCm39) |
F10L |
probably benign |
Het |
Dhrs2 |
T |
A |
14: 55,477,928 (GRCm39) |
I220N |
probably damaging |
Het |
Dlg5 |
T |
C |
14: 24,198,328 (GRCm39) |
D1535G |
possibly damaging |
Het |
Dpy19l1 |
A |
G |
9: 24,414,372 (GRCm39) |
S19P |
probably benign |
Het |
Eif3l |
A |
C |
15: 78,963,220 (GRCm39) |
E134A |
possibly damaging |
Het |
Epb41 |
C |
A |
4: 131,664,772 (GRCm39) |
V90L |
|
Het |
Flad1 |
A |
T |
3: 89,316,109 (GRCm39) |
V151D |
probably damaging |
Het |
Gja10 |
A |
T |
4: 32,601,568 (GRCm39) |
I272N |
probably benign |
Het |
Glmp |
T |
A |
3: 88,233,580 (GRCm39) |
D178E |
probably benign |
Het |
Gm16494 |
G |
A |
17: 47,327,750 (GRCm39) |
P45S |
probably damaging |
Het |
Gm4553 |
T |
C |
7: 141,719,458 (GRCm39) |
D6G |
unknown |
Het |
Grid2 |
G |
A |
6: 63,233,929 (GRCm39) |
|
probably null |
Het |
Icmt |
A |
G |
4: 152,387,482 (GRCm39) |
M226V |
probably benign |
Het |
Igkv5-39 |
T |
C |
6: 69,877,607 (GRCm39) |
S50G |
probably benign |
Het |
Ints5 |
T |
C |
19: 8,872,484 (GRCm39) |
S148P |
probably damaging |
Het |
Itga2b |
A |
C |
11: 102,351,985 (GRCm39) |
V504G |
possibly damaging |
Het |
Krt20 |
T |
A |
11: 99,323,063 (GRCm39) |
Y253F |
probably damaging |
Het |
Man2a2 |
T |
A |
7: 80,018,656 (GRCm39) |
I68L |
probably damaging |
Het |
Mpi |
G |
A |
9: 57,455,954 (GRCm39) |
T176I |
probably benign |
Het |
Msh6 |
C |
T |
17: 88,294,340 (GRCm39) |
R1032C |
probably damaging |
Het |
Myot |
C |
T |
18: 44,475,416 (GRCm39) |
T179I |
probably damaging |
Het |
Neb |
A |
G |
2: 52,116,601 (GRCm39) |
S946P |
|
Het |
Notch3 |
G |
A |
17: 32,341,713 (GRCm39) |
A2013V |
probably damaging |
Het |
Nr1d1 |
T |
C |
11: 98,662,133 (GRCm39) |
Y167C |
probably damaging |
Het |
Or52h7 |
T |
A |
7: 104,213,593 (GRCm39) |
F55Y |
probably benign |
Het |
Or52n2c |
T |
C |
7: 104,574,828 (GRCm39) |
I48V |
probably benign |
Het |
Or7g32 |
A |
G |
9: 19,408,377 (GRCm39) |
E111G |
probably damaging |
Het |
Or8k40 |
A |
C |
2: 86,584,893 (GRCm39) |
L63R |
probably damaging |
Het |
P4ha3 |
G |
A |
7: 99,966,309 (GRCm39) |
V485M |
probably damaging |
Het |
Pbk |
T |
A |
14: 66,054,185 (GRCm39) |
C243* |
probably null |
Het |
Pde4b |
T |
A |
4: 102,459,983 (GRCm39) |
L388H |
possibly damaging |
Het |
Pecam1 |
T |
C |
11: 106,579,745 (GRCm39) |
D439G |
probably benign |
Het |
Pknox2 |
A |
T |
9: 36,822,459 (GRCm39) |
M230K |
probably benign |
Het |
Plekhh2 |
A |
G |
17: 84,908,113 (GRCm39) |
I1185V |
probably damaging |
Het |
Polr3g |
A |
G |
13: 81,842,682 (GRCm39) |
V111A |
unknown |
Het |
Rftn1 |
G |
T |
17: 50,354,408 (GRCm39) |
A318D |
probably damaging |
Het |
Rnf123 |
A |
T |
9: 107,940,089 (GRCm39) |
V768D |
probably damaging |
Het |
Rps16 |
T |
A |
7: 28,052,008 (GRCm39) |
S129T |
probably benign |
Het |
Scg2 |
A |
T |
1: 79,413,222 (GRCm39) |
N460K |
probably benign |
Het |
Sct |
T |
C |
7: 140,858,807 (GRCm39) |
S42G |
probably damaging |
Het |
Spef2 |
A |
T |
15: 9,727,629 (GRCm39) |
N151K |
probably benign |
Het |
Syce1l |
C |
A |
8: 114,380,721 (GRCm39) |
D144E |
possibly damaging |
Het |
Syt17 |
T |
C |
7: 118,036,069 (GRCm39) |
Y99C |
probably damaging |
Het |
Tgfbr3 |
T |
C |
5: 107,287,640 (GRCm39) |
N520D |
probably damaging |
Het |
Thsd7b |
A |
G |
1: 129,523,193 (GRCm39) |
S76G |
probably benign |
Het |
Tmem63a |
G |
T |
1: 180,788,685 (GRCm39) |
V341F |
probably benign |
Het |
Trim5 |
A |
G |
7: 103,914,993 (GRCm39) |
S359P |
probably damaging |
Het |
Tst |
A |
T |
15: 78,284,020 (GRCm39) |
V269E |
probably damaging |
Het |
Ubr3 |
A |
T |
2: 69,784,706 (GRCm39) |
I808F |
probably null |
Het |
Ugt3a1 |
T |
A |
15: 9,362,024 (GRCm39) |
Y267N |
probably benign |
Het |
Wwc1 |
A |
T |
11: 35,761,384 (GRCm39) |
|
probably benign |
Het |
Zfp36l2 |
G |
T |
17: 84,494,552 (GRCm39) |
N28K |
probably damaging |
Het |
Zfp57 |
A |
G |
17: 37,321,136 (GRCm39) |
D330G |
probably benign |
Het |
Zgrf1 |
C |
A |
3: 127,377,644 (GRCm39) |
S963Y |
probably damaging |
Het |
Zranb2 |
A |
G |
3: 157,247,412 (GRCm39) |
K197E |
unknown |
Het |
|
Other mutations in Prkcg |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01449:Prkcg
|
APN |
7 |
3,368,135 (GRCm39) |
missense |
probably benign |
0.27 |
IGL01551:Prkcg
|
APN |
7 |
3,352,342 (GRCm39) |
unclassified |
probably benign |
|
IGL02167:Prkcg
|
APN |
7 |
3,371,097 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02434:Prkcg
|
APN |
7 |
3,367,406 (GRCm39) |
missense |
probably benign |
|
R0044:Prkcg
|
UTSW |
7 |
3,363,517 (GRCm39) |
intron |
probably benign |
|
R0164:Prkcg
|
UTSW |
7 |
3,377,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R0164:Prkcg
|
UTSW |
7 |
3,377,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R0413:Prkcg
|
UTSW |
7 |
3,368,095 (GRCm39) |
missense |
probably benign |
0.00 |
R0417:Prkcg
|
UTSW |
7 |
3,352,820 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1113:Prkcg
|
UTSW |
7 |
3,377,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R1170:Prkcg
|
UTSW |
7 |
3,368,177 (GRCm39) |
missense |
probably damaging |
0.97 |
R1308:Prkcg
|
UTSW |
7 |
3,377,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R1634:Prkcg
|
UTSW |
7 |
3,371,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R1978:Prkcg
|
UTSW |
7 |
3,353,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R2016:Prkcg
|
UTSW |
7 |
3,372,066 (GRCm39) |
missense |
probably damaging |
0.98 |
R2209:Prkcg
|
UTSW |
7 |
3,352,097 (GRCm39) |
unclassified |
probably benign |
|
R3788:Prkcg
|
UTSW |
7 |
3,362,263 (GRCm39) |
missense |
probably damaging |
0.99 |
R4006:Prkcg
|
UTSW |
7 |
3,375,983 (GRCm39) |
missense |
probably damaging |
0.96 |
R4853:Prkcg
|
UTSW |
7 |
3,367,469 (GRCm39) |
missense |
probably damaging |
0.99 |
R4915:Prkcg
|
UTSW |
7 |
3,378,781 (GRCm39) |
nonsense |
probably null |
|
R4916:Prkcg
|
UTSW |
7 |
3,378,781 (GRCm39) |
nonsense |
probably null |
|
R4997:Prkcg
|
UTSW |
7 |
3,371,097 (GRCm39) |
critical splice donor site |
probably null |
|
R5446:Prkcg
|
UTSW |
7 |
3,378,780 (GRCm39) |
missense |
probably benign |
0.00 |
R5646:Prkcg
|
UTSW |
7 |
3,377,597 (GRCm39) |
missense |
probably damaging |
0.97 |
R5677:Prkcg
|
UTSW |
7 |
3,371,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R6913:Prkcg
|
UTSW |
7 |
3,362,335 (GRCm39) |
missense |
probably benign |
0.02 |
R7355:Prkcg
|
UTSW |
7 |
3,372,025 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7371:Prkcg
|
UTSW |
7 |
3,368,069 (GRCm39) |
missense |
probably benign |
0.27 |
R7544:Prkcg
|
UTSW |
7 |
3,359,081 (GRCm39) |
missense |
probably benign |
0.00 |
R7649:Prkcg
|
UTSW |
7 |
3,378,480 (GRCm39) |
missense |
probably benign |
0.09 |
R7742:Prkcg
|
UTSW |
7 |
3,378,459 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8009:Prkcg
|
UTSW |
7 |
3,362,708 (GRCm39) |
missense |
probably benign |
|
R8074:Prkcg
|
UTSW |
7 |
3,372,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R8344:Prkcg
|
UTSW |
7 |
3,378,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R8887:Prkcg
|
UTSW |
7 |
3,370,857 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9343:Prkcg
|
UTSW |
7 |
3,359,124 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9426:Prkcg
|
UTSW |
7 |
3,375,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R9530:Prkcg
|
UTSW |
7 |
3,375,965 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9605:Prkcg
|
UTSW |
7 |
3,359,360 (GRCm39) |
missense |
probably benign |
0.01 |
|