Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
T |
A |
7: 120,119,283 (GRCm39) |
I1009N |
possibly damaging |
Het |
Abtb3 |
C |
A |
10: 85,224,079 (GRCm39) |
A296E |
unknown |
Het |
Adcy8 |
T |
A |
15: 64,571,095 (GRCm39) |
N1213Y |
probably benign |
Het |
Ahctf1 |
T |
C |
1: 179,581,433 (GRCm39) |
S1590G |
possibly damaging |
Het |
Ahcyl1 |
A |
T |
3: 107,577,588 (GRCm39) |
N277K |
probably damaging |
Het |
Ank2 |
A |
T |
3: 126,740,149 (GRCm39) |
S1912T |
unknown |
Het |
Ank3 |
T |
A |
10: 69,733,957 (GRCm39) |
N740K |
unknown |
Het |
Atp13a3 |
A |
C |
16: 30,159,051 (GRCm39) |
I800S |
probably benign |
Het |
AU041133 |
T |
A |
10: 81,986,679 (GRCm39) |
C111S |
probably damaging |
Het |
Azi2 |
T |
A |
9: 117,884,924 (GRCm39) |
I211N |
probably benign |
Het |
Camk2b |
T |
C |
11: 5,922,408 (GRCm39) |
N480S |
probably damaging |
Het |
Card6 |
A |
G |
15: 5,128,702 (GRCm39) |
V898A |
probably benign |
Het |
Copb2 |
T |
A |
9: 98,461,081 (GRCm39) |
M381K |
probably damaging |
Het |
Cplx3 |
T |
C |
9: 57,523,060 (GRCm39) |
D133G |
probably damaging |
Het |
Crisp1 |
A |
T |
17: 40,616,071 (GRCm39) |
M102K |
probably damaging |
Het |
Dcxr |
A |
T |
11: 120,618,084 (GRCm39) |
|
probably benign |
Het |
Dennd5a |
C |
A |
7: 109,500,374 (GRCm39) |
R917L |
probably benign |
Het |
Egflam |
T |
A |
15: 7,279,525 (GRCm39) |
T494S |
probably benign |
Het |
Fkbpl |
T |
A |
17: 34,864,691 (GRCm39) |
M153K |
probably benign |
Het |
Helz2 |
A |
T |
2: 180,882,616 (GRCm39) |
I59N |
probably damaging |
Het |
Ldlrap1 |
T |
C |
4: 134,477,303 (GRCm39) |
T194A |
probably benign |
Het |
Lrrc27 |
T |
C |
7: 138,807,913 (GRCm39) |
M340T |
probably benign |
Het |
Lum |
T |
A |
10: 97,404,157 (GRCm39) |
S17R |
probably benign |
Het |
Malrd1 |
A |
G |
2: 15,847,405 (GRCm39) |
K1182E |
unknown |
Het |
Map3k2 |
A |
T |
18: 32,333,069 (GRCm39) |
D81V |
possibly damaging |
Het |
Muc5b |
A |
T |
7: 141,415,480 (GRCm39) |
T2809S |
possibly damaging |
Het |
Nle1 |
C |
A |
11: 82,793,876 (GRCm39) |
V387L |
probably benign |
Het |
Nr1h4 |
T |
C |
10: 89,290,618 (GRCm39) |
D474G |
probably benign |
Het |
Nup205 |
T |
C |
6: 35,163,468 (GRCm39) |
I144T |
possibly damaging |
Het |
Or10ag57 |
G |
T |
2: 87,218,508 (GRCm39) |
C153F |
probably damaging |
Het |
Or1e17 |
C |
A |
11: 73,831,986 (GRCm39) |
L305I |
probably benign |
Het |
Or2a56 |
A |
T |
6: 42,933,091 (GRCm39) |
I220F |
probably damaging |
Het |
Or4f15 |
G |
A |
2: 111,814,194 (GRCm39) |
S75L |
possibly damaging |
Het |
Or4n4 |
G |
A |
14: 50,519,701 (GRCm39) |
T3I |
probably benign |
Het |
Or51f1 |
T |
C |
7: 102,506,093 (GRCm39) |
Y132C |
probably benign |
Het |
Pkn3 |
C |
T |
2: 29,973,290 (GRCm39) |
R371* |
probably null |
Het |
Plin2 |
A |
T |
4: 86,586,742 (GRCm39) |
S30T |
possibly damaging |
Het |
Ppfibp1 |
T |
C |
6: 146,917,769 (GRCm39) |
V475A |
probably benign |
Het |
Rasgrf2 |
T |
A |
13: 92,267,860 (GRCm39) |
Q48L |
probably damaging |
Het |
Rnf168 |
G |
C |
16: 32,117,386 (GRCm39) |
V316L |
probably benign |
Het |
Shank1 |
G |
A |
7: 43,962,342 (GRCm39) |
S71N |
unknown |
Het |
Spata31d1d |
T |
C |
13: 59,874,637 (GRCm39) |
H966R |
possibly damaging |
Het |
Speg |
C |
A |
1: 75,399,358 (GRCm39) |
D2268E |
probably benign |
Het |
Srp54c |
A |
G |
12: 55,296,811 (GRCm39) |
I170V |
probably benign |
Het |
Syde2 |
A |
G |
3: 145,704,364 (GRCm39) |
R439G |
probably benign |
Het |
Tcof1 |
T |
C |
18: 60,949,558 (GRCm39) |
K1155R |
unknown |
Het |
Tmem184c |
T |
C |
8: 78,323,087 (GRCm39) |
I592V |
probably benign |
Het |
Trav6-7-dv9 |
A |
G |
14: 53,947,669 (GRCm39) |
Y57C |
probably damaging |
Het |
Trpc1 |
T |
A |
9: 95,625,303 (GRCm39) |
I108F |
probably damaging |
Het |
Virma |
A |
T |
4: 11,546,007 (GRCm39) |
H1615L |
probably damaging |
Het |
Vmn2r10 |
A |
T |
5: 109,150,404 (GRCm39) |
D213E |
probably damaging |
Het |
Vmn2r116 |
T |
A |
17: 23,620,399 (GRCm39) |
V711E |
probably damaging |
Het |
Vps16 |
T |
C |
2: 130,282,405 (GRCm39) |
F413L |
probably benign |
Het |
Vwa1 |
G |
A |
4: 155,857,336 (GRCm39) |
P154L |
probably damaging |
Het |
Wasf1 |
T |
C |
10: 40,812,693 (GRCm39) |
I494T |
unknown |
Het |
Wdr36 |
A |
G |
18: 32,985,700 (GRCm39) |
D539G |
possibly damaging |
Het |
Zfp81 |
A |
T |
17: 33,554,411 (GRCm39) |
C134* |
probably null |
Het |
|
Other mutations in Ppp2ca |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00434:Ppp2ca
|
APN |
11 |
52,012,776 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01767:Ppp2ca
|
APN |
11 |
52,008,882 (GRCm39) |
nonsense |
probably null |
|
IGL01982:Ppp2ca
|
APN |
11 |
51,989,891 (GRCm39) |
missense |
probably benign |
|
IGL03260:Ppp2ca
|
APN |
11 |
52,003,975 (GRCm39) |
missense |
probably damaging |
0.96 |
R0539:Ppp2ca
|
UTSW |
11 |
52,008,989 (GRCm39) |
critical splice donor site |
probably null |
|
R0788:Ppp2ca
|
UTSW |
11 |
52,003,969 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0855:Ppp2ca
|
UTSW |
11 |
52,012,752 (GRCm39) |
missense |
probably benign |
0.01 |
R1539:Ppp2ca
|
UTSW |
11 |
52,011,800 (GRCm39) |
missense |
probably damaging |
0.99 |
R1591:Ppp2ca
|
UTSW |
11 |
51,989,916 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1766:Ppp2ca
|
UTSW |
11 |
52,012,773 (GRCm39) |
missense |
probably benign |
|
R2267:Ppp2ca
|
UTSW |
11 |
52,008,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R2268:Ppp2ca
|
UTSW |
11 |
52,008,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R3933:Ppp2ca
|
UTSW |
11 |
52,010,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R4199:Ppp2ca
|
UTSW |
11 |
51,989,928 (GRCm39) |
missense |
probably benign |
|
R4992:Ppp2ca
|
UTSW |
11 |
52,004,033 (GRCm39) |
missense |
possibly damaging |
0.52 |
R5261:Ppp2ca
|
UTSW |
11 |
51,989,937 (GRCm39) |
missense |
probably benign |
|
R5684:Ppp2ca
|
UTSW |
11 |
52,004,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R5729:Ppp2ca
|
UTSW |
11 |
52,008,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R5766:Ppp2ca
|
UTSW |
11 |
52,004,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R7186:Ppp2ca
|
UTSW |
11 |
52,010,080 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8073:Ppp2ca
|
UTSW |
11 |
52,010,124 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9014:Ppp2ca
|
UTSW |
11 |
52,009,510 (GRCm39) |
missense |
probably damaging |
1.00 |
|