Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Afg3l2 |
T |
C |
18: 67,556,023 (GRCm39) |
E436G |
probably damaging |
Het |
Agbl5 |
T |
A |
5: 31,060,583 (GRCm39) |
L759* |
probably null |
Het |
Ankrd13b |
T |
C |
11: 77,363,583 (GRCm39) |
D460G |
probably benign |
Het |
Apol10a |
A |
G |
15: 77,373,225 (GRCm39) |
D287G |
possibly damaging |
Het |
Arhgap44 |
A |
T |
11: 64,915,094 (GRCm39) |
Y391* |
probably null |
Het |
Asz1 |
G |
T |
6: 18,074,900 (GRCm39) |
S271R |
probably benign |
Het |
AW554918 |
A |
G |
18: 25,473,170 (GRCm39) |
N325D |
probably benign |
Het |
Brinp2 |
A |
T |
1: 158,082,579 (GRCm39) |
L247Q |
probably damaging |
Het |
Casz1 |
A |
G |
4: 149,036,850 (GRCm39) |
D1704G |
unknown |
Het |
Cdk5rap1 |
G |
A |
2: 154,202,595 (GRCm39) |
R212W |
probably damaging |
Het |
Cdkl2 |
T |
A |
5: 92,167,318 (GRCm39) |
T444S |
probably benign |
Het |
Cers2 |
T |
G |
3: 95,228,656 (GRCm39) |
F160V |
probably benign |
Het |
Cfap276 |
T |
C |
3: 108,450,815 (GRCm39) |
F86L |
possibly damaging |
Het |
Cga |
T |
A |
4: 34,907,076 (GRCm39) |
M99K |
probably benign |
Het |
Cspp1 |
C |
T |
1: 10,135,572 (GRCm39) |
R138* |
probably null |
Het |
Dao |
T |
G |
5: 114,153,273 (GRCm39) |
*133E |
probably null |
Het |
Ddx1 |
A |
T |
12: 13,275,456 (GRCm39) |
C544S |
probably null |
Het |
Dgkq |
A |
T |
5: 108,806,112 (GRCm39) |
V98E |
probably damaging |
Het |
Dnah6 |
T |
A |
6: 73,169,300 (GRCm39) |
T434S |
possibly damaging |
Het |
Dntt |
A |
G |
19: 41,027,418 (GRCm39) |
N162D |
probably benign |
Het |
Dpysl5 |
T |
C |
5: 30,902,805 (GRCm39) |
V79A |
probably benign |
Het |
Efcab3 |
T |
C |
11: 104,611,871 (GRCm39) |
L571P |
probably damaging |
Het |
Ep300 |
T |
C |
15: 81,532,567 (GRCm39) |
C1602R |
unknown |
Het |
Flrt3 |
C |
T |
2: 140,503,672 (GRCm39) |
|
probably null |
Het |
Gnpat |
T |
G |
8: 125,614,553 (GRCm39) |
M663R |
probably benign |
Het |
Hc |
A |
T |
2: 34,874,859 (GRCm39) |
|
probably null |
Het |
Il12rb1 |
A |
G |
8: 71,263,271 (GRCm39) |
Y67C |
probably damaging |
Het |
Ints15 |
G |
A |
5: 143,297,600 (GRCm39) |
A149V |
probably benign |
Het |
Kmt2b |
C |
T |
7: 30,281,385 (GRCm39) |
D1229N |
probably damaging |
Het |
Lamc1 |
T |
C |
1: 153,124,822 (GRCm39) |
T650A |
probably damaging |
Het |
Lrp1 |
G |
A |
10: 127,419,766 (GRCm39) |
R948* |
probably null |
Het |
Map3k21 |
T |
C |
8: 126,654,336 (GRCm39) |
I385T |
probably damaging |
Het |
Mmrn1 |
T |
A |
6: 60,953,236 (GRCm39) |
S506T |
probably benign |
Het |
Nlrp1a |
A |
G |
11: 71,014,023 (GRCm39) |
F409S |
probably damaging |
Het |
Nlrp3 |
T |
A |
11: 59,455,892 (GRCm39) |
I896N |
probably benign |
Het |
Noxred1 |
C |
A |
12: 87,273,799 (GRCm39) |
V81L |
probably damaging |
Het |
Nrcam |
A |
T |
12: 44,645,272 (GRCm39) |
I1225F |
probably damaging |
Het |
Or2z2 |
C |
T |
11: 58,346,481 (GRCm39) |
C98Y |
probably damaging |
Het |
Otos |
T |
A |
1: 92,572,241 (GRCm39) |
|
probably null |
Het |
Pcdh20 |
A |
G |
14: 88,706,103 (GRCm39) |
I399T |
probably benign |
Het |
Pkhd1 |
C |
T |
1: 20,309,528 (GRCm39) |
V2807I |
not run |
Het |
Prrx2 |
A |
G |
2: 30,770,902 (GRCm39) |
E235G |
probably damaging |
Het |
Rab13 |
T |
C |
3: 90,128,327 (GRCm39) |
I41T |
probably damaging |
Het |
Rai1 |
A |
C |
11: 60,080,201 (GRCm39) |
T1422P |
possibly damaging |
Het |
Rcn1 |
C |
T |
2: 105,222,336 (GRCm39) |
V217M |
probably damaging |
Het |
Scn2a |
T |
A |
2: 65,518,998 (GRCm39) |
V408E |
probably damaging |
Het |
Sec16a |
C |
T |
2: 26,318,376 (GRCm39) |
A121T |
|
Het |
Slc35d1 |
A |
G |
4: 103,046,982 (GRCm39) |
|
probably null |
Het |
Slc39a6 |
A |
T |
18: 24,717,106 (GRCm39) |
V642E |
probably damaging |
Het |
Slc6a19 |
G |
A |
13: 73,841,203 (GRCm39) |
A69V |
probably benign |
Het |
Spink6 |
A |
T |
18: 44,215,386 (GRCm39) |
T79S |
probably damaging |
Het |
Spire1 |
T |
C |
18: 67,652,950 (GRCm39) |
D170G |
probably damaging |
Het |
Sugp1 |
T |
C |
8: 70,505,269 (GRCm39) |
S79P |
probably damaging |
Het |
Syne3 |
A |
G |
12: 104,934,167 (GRCm39) |
Y201H |
probably damaging |
Het |
Tbc1d10a |
T |
C |
11: 4,155,858 (GRCm39) |
|
probably null |
Het |
Tmem14a |
C |
T |
1: 21,299,735 (GRCm39) |
Q122* |
probably null |
Het |
Tmem161b |
C |
A |
13: 84,370,537 (GRCm39) |
|
probably benign |
Het |
Trmt61a |
A |
G |
12: 111,645,321 (GRCm39) |
I86V |
possibly damaging |
Het |
Tubgcp4 |
G |
A |
2: 121,020,447 (GRCm39) |
|
probably null |
Het |
Vmn1r79 |
T |
A |
7: 11,910,668 (GRCm39) |
Y183* |
probably null |
Het |
Vmn2r11 |
A |
T |
5: 109,202,742 (GRCm39) |
W112R |
probably benign |
Het |
Vpreb1a |
T |
C |
16: 16,686,516 (GRCm39) |
K125E |
probably benign |
Het |
Wdr6 |
A |
T |
9: 108,451,971 (GRCm39) |
F637L |
probably damaging |
Het |
|
Other mutations in Gk2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01519:Gk2
|
APN |
5 |
97,603,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R0967:Gk2
|
UTSW |
5 |
97,604,155 (GRCm39) |
missense |
probably benign |
|
R1307:Gk2
|
UTSW |
5 |
97,603,268 (GRCm39) |
missense |
probably benign |
|
R2111:Gk2
|
UTSW |
5 |
97,604,164 (GRCm39) |
missense |
probably benign |
0.00 |
R3939:Gk2
|
UTSW |
5 |
97,603,211 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4646:Gk2
|
UTSW |
5 |
97,604,056 (GRCm39) |
missense |
probably damaging |
0.98 |
R4648:Gk2
|
UTSW |
5 |
97,603,579 (GRCm39) |
missense |
probably benign |
0.04 |
R4718:Gk2
|
UTSW |
5 |
97,603,725 (GRCm39) |
missense |
probably benign |
0.02 |
R6139:Gk2
|
UTSW |
5 |
97,604,139 (GRCm39) |
missense |
probably benign |
0.03 |
R6792:Gk2
|
UTSW |
5 |
97,603,588 (GRCm39) |
missense |
probably benign |
0.02 |
R7078:Gk2
|
UTSW |
5 |
97,604,195 (GRCm39) |
missense |
probably benign |
0.00 |
R7088:Gk2
|
UTSW |
5 |
97,603,534 (GRCm39) |
missense |
probably damaging |
0.97 |
R7699:Gk2
|
UTSW |
5 |
97,604,257 (GRCm39) |
missense |
probably benign |
|
R8766:Gk2
|
UTSW |
5 |
97,604,110 (GRCm39) |
missense |
probably benign |
0.00 |
R8878:Gk2
|
UTSW |
5 |
97,604,341 (GRCm39) |
missense |
probably benign |
0.00 |
X0062:Gk2
|
UTSW |
5 |
97,604,508 (GRCm39) |
missense |
possibly damaging |
0.93 |
|