Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agmo |
C |
T |
12: 37,302,480 (GRCm39) |
L106F |
probably benign |
Het |
Appl1 |
A |
G |
14: 26,673,473 (GRCm39) |
I208T |
possibly damaging |
Het |
Arap2 |
G |
T |
5: 62,906,452 (GRCm39) |
A189D |
probably benign |
Het |
Arhgef12 |
T |
C |
9: 42,883,324 (GRCm39) |
K1402E |
possibly damaging |
Het |
C7 |
A |
C |
15: 5,079,042 (GRCm39) |
F89V |
probably damaging |
Het |
Camsap2 |
G |
A |
1: 136,208,861 (GRCm39) |
T877I |
probably damaging |
Het |
Cpt2 |
T |
C |
4: 107,764,583 (GRCm39) |
T394A |
probably benign |
Het |
Dnah10 |
C |
A |
5: 124,875,078 (GRCm39) |
T2528N |
probably damaging |
Het |
Entpd8 |
G |
T |
2: 24,975,151 (GRCm39) |
W494L |
probably damaging |
Het |
Fam114a1 |
T |
A |
5: 65,163,135 (GRCm39) |
|
probably benign |
Het |
Fat4 |
T |
C |
3: 38,943,444 (GRCm39) |
V779A |
probably damaging |
Het |
Gckr |
T |
C |
5: 31,455,548 (GRCm39) |
S34P |
probably damaging |
Het |
Golga4 |
T |
C |
9: 118,364,528 (GRCm39) |
V297A |
probably benign |
Het |
Gpr65 |
T |
C |
12: 98,241,469 (GRCm39) |
S41P |
probably damaging |
Het |
Gps1 |
G |
T |
11: 120,677,649 (GRCm39) |
A221S |
probably damaging |
Het |
Heatr1 |
T |
A |
13: 12,448,867 (GRCm39) |
S1861T |
probably damaging |
Het |
Hmces |
A |
G |
6: 87,902,711 (GRCm39) |
E184G |
probably damaging |
Het |
Itfg1 |
T |
C |
8: 86,452,140 (GRCm39) |
|
probably null |
Het |
Mrtfb |
C |
T |
16: 13,221,020 (GRCm39) |
T743I |
possibly damaging |
Het |
Nfe2l3 |
A |
G |
6: 51,434,291 (GRCm39) |
S284G |
possibly damaging |
Het |
Nlrp2 |
C |
A |
7: 5,331,317 (GRCm39) |
A360S |
probably damaging |
Het |
Nop9 |
A |
G |
14: 55,987,533 (GRCm39) |
H298R |
probably benign |
Het |
Or5an1 |
A |
T |
19: 12,261,347 (GRCm39) |
S312C |
possibly damaging |
Het |
Or5h17 |
T |
A |
16: 58,820,321 (GRCm39) |
V91E |
probably benign |
Het |
Or6ae1 |
T |
C |
7: 139,742,287 (GRCm39) |
D192G |
possibly damaging |
Het |
Osgin1 |
A |
G |
8: 120,170,006 (GRCm39) |
M158V |
probably benign |
Het |
Patj |
C |
A |
4: 98,314,301 (GRCm39) |
Q374K |
probably damaging |
Het |
Pck1 |
G |
T |
2: 172,997,797 (GRCm39) |
G289W |
probably damaging |
Het |
Phkg1 |
T |
G |
5: 129,894,895 (GRCm39) |
I219L |
possibly damaging |
Het |
Ppp1r15b |
G |
A |
1: 133,061,081 (GRCm39) |
A533T |
probably damaging |
Het |
Ppwd1 |
T |
C |
13: 104,350,192 (GRCm39) |
I398V |
probably benign |
Het |
Prkdc |
A |
G |
16: 15,651,530 (GRCm39) |
|
probably benign |
Het |
Psg25 |
G |
A |
7: 18,260,212 (GRCm39) |
L229F |
possibly damaging |
Het |
Rps6ka1 |
T |
A |
4: 133,608,265 (GRCm39) |
Q24L |
probably benign |
Het |
Sgk3 |
T |
C |
1: 9,949,273 (GRCm39) |
I147T |
possibly damaging |
Het |
Slc25a24 |
T |
A |
3: 109,062,387 (GRCm39) |
I159N |
probably damaging |
Het |
Slc26a4 |
T |
C |
12: 31,572,526 (GRCm39) |
|
probably null |
Het |
Slc35f4 |
T |
C |
14: 49,541,714 (GRCm39) |
I347V |
probably benign |
Het |
Spag17 |
A |
T |
3: 100,016,713 (GRCm39) |
M2163L |
probably benign |
Het |
Stab2 |
C |
T |
10: 86,786,133 (GRCm39) |
|
probably benign |
Het |
Sult2a8 |
G |
A |
7: 14,145,630 (GRCm39) |
|
probably benign |
Het |
Syne2 |
T |
C |
12: 76,078,320 (GRCm39) |
L4718P |
probably damaging |
Het |
Timd4 |
G |
T |
11: 46,706,521 (GRCm39) |
G108W |
probably damaging |
Het |
Timm9 |
T |
C |
12: 71,173,148 (GRCm39) |
|
probably benign |
Het |
Vmn2r98 |
G |
A |
17: 19,286,275 (GRCm39) |
V258I |
probably benign |
Het |
Zcchc9 |
C |
T |
13: 91,949,000 (GRCm39) |
V174I |
probably benign |
Het |
Zdbf2 |
T |
C |
1: 63,342,236 (GRCm39) |
V205A |
possibly damaging |
Het |
|
Other mutations in Csnk2a1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01571:Csnk2a1
|
APN |
2 |
152,117,326 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02003:Csnk2a1
|
APN |
2 |
152,118,890 (GRCm39) |
nonsense |
probably null |
|
IGL02043:Csnk2a1
|
APN |
2 |
152,116,070 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02815:Csnk2a1
|
APN |
2 |
152,116,005 (GRCm39) |
splice site |
probably benign |
|
IGL02818:Csnk2a1
|
APN |
2 |
152,116,005 (GRCm39) |
splice site |
probably benign |
|
IGL02819:Csnk2a1
|
APN |
2 |
152,116,005 (GRCm39) |
splice site |
probably benign |
|
R1454:Csnk2a1
|
UTSW |
2 |
152,099,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R1725:Csnk2a1
|
UTSW |
2 |
152,099,892 (GRCm39) |
missense |
probably damaging |
0.98 |
R2086:Csnk2a1
|
UTSW |
2 |
152,096,201 (GRCm39) |
missense |
probably benign |
0.01 |
R3113:Csnk2a1
|
UTSW |
2 |
152,105,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R4003:Csnk2a1
|
UTSW |
2 |
152,092,495 (GRCm39) |
missense |
probably damaging |
0.97 |
R4021:Csnk2a1
|
UTSW |
2 |
152,100,609 (GRCm39) |
missense |
probably damaging |
0.96 |
R6702:Csnk2a1
|
UTSW |
2 |
152,100,608 (GRCm39) |
missense |
probably benign |
0.35 |
R6703:Csnk2a1
|
UTSW |
2 |
152,100,608 (GRCm39) |
missense |
probably benign |
0.35 |
R6849:Csnk2a1
|
UTSW |
2 |
152,092,484 (GRCm39) |
missense |
probably benign |
|
R7021:Csnk2a1
|
UTSW |
2 |
152,102,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R7061:Csnk2a1
|
UTSW |
2 |
152,116,091 (GRCm39) |
missense |
probably benign |
0.08 |
R7381:Csnk2a1
|
UTSW |
2 |
152,100,614 (GRCm39) |
missense |
probably benign |
0.05 |
R8799:Csnk2a1
|
UTSW |
2 |
152,099,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R8990:Csnk2a1
|
UTSW |
2 |
152,096,177 (GRCm39) |
missense |
probably damaging |
1.00 |
|