Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610028H24Rik |
A |
C |
10: 76,285,096 (GRCm39) |
T2P |
possibly damaging |
Het |
2610042L04Rik |
A |
G |
14: 4,348,962 (GRCm38) |
N41S |
probably damaging |
Het |
4933402N03Rik |
T |
C |
7: 130,747,863 (GRCm39) |
D43G |
probably benign |
Het |
Adcy10 |
C |
A |
1: 165,403,297 (GRCm39) |
Y1598* |
probably null |
Het |
Adgrv1 |
G |
A |
13: 81,614,402 (GRCm39) |
T3997M |
probably benign |
Het |
Amfr |
A |
C |
8: 94,726,992 (GRCm39) |
F74V |
probably damaging |
Het |
Ankrd13a |
T |
C |
5: 114,924,787 (GRCm39) |
Y91H |
probably benign |
Het |
Baiap3 |
A |
G |
17: 25,464,732 (GRCm39) |
S767P |
probably benign |
Het |
Car12 |
C |
T |
9: 66,661,008 (GRCm39) |
T124I |
probably damaging |
Het |
Casp9 |
G |
T |
4: 141,534,448 (GRCm39) |
G286V |
probably damaging |
Het |
Cc2d2a |
T |
A |
5: 43,828,577 (GRCm39) |
D18E |
probably benign |
Het |
Cdc27 |
T |
C |
11: 104,419,270 (GRCm39) |
N221D |
probably damaging |
Het |
Cebpz |
A |
G |
17: 79,244,339 (GRCm39) |
S41P |
possibly damaging |
Het |
Cenpo |
T |
A |
12: 4,281,968 (GRCm39) |
S10C |
possibly damaging |
Het |
Chid1 |
A |
G |
7: 141,076,049 (GRCm39) |
V368A |
probably benign |
Het |
Clca3a1 |
C |
A |
3: 144,714,716 (GRCm39) |
V634L |
probably benign |
Het |
Cmtr1 |
A |
G |
17: 29,901,122 (GRCm39) |
D683G |
probably damaging |
Het |
Cpsf3 |
G |
T |
12: 21,350,163 (GRCm39) |
R294L |
probably damaging |
Het |
Ddrgk1 |
G |
A |
2: 130,496,599 (GRCm39) |
T255M |
possibly damaging |
Het |
Dennd6a |
T |
A |
14: 26,337,813 (GRCm39) |
|
probably null |
Het |
Dnah10 |
A |
G |
5: 124,820,743 (GRCm39) |
R526G |
probably damaging |
Het |
Dock3 |
G |
A |
9: 106,790,147 (GRCm39) |
T1484I |
probably benign |
Het |
Efcab10 |
T |
C |
12: 33,448,433 (GRCm39) |
Y89H |
probably damaging |
Het |
Etl4 |
T |
A |
2: 20,806,379 (GRCm39) |
D1200E |
probably damaging |
Het |
Fbn1 |
T |
A |
2: 125,166,865 (GRCm39) |
D2017V |
probably damaging |
Het |
Ftmt |
G |
A |
18: 52,465,307 (GRCm39) |
V208M |
probably damaging |
Het |
Fzd10 |
T |
C |
5: 128,679,995 (GRCm39) |
Y572H |
probably damaging |
Het |
Gcc1 |
T |
C |
6: 28,420,742 (GRCm39) |
K39E |
probably damaging |
Het |
Hydin |
A |
G |
8: 111,118,743 (GRCm39) |
|
probably null |
Het |
Lif |
A |
G |
11: 4,218,940 (GRCm39) |
E73G |
possibly damaging |
Het |
Lrtm1 |
C |
A |
14: 28,749,628 (GRCm39) |
Q357K |
probably benign |
Het |
Mef2d |
T |
A |
3: 88,066,852 (GRCm39) |
L205Q |
probably damaging |
Het |
Naalad2 |
T |
A |
9: 18,296,361 (GRCm39) |
E96D |
probably damaging |
Het |
Nbas |
T |
C |
12: 13,532,596 (GRCm39) |
I1768T |
probably benign |
Het |
Nodal |
T |
C |
10: 61,259,258 (GRCm39) |
S232P |
probably damaging |
Het |
Or52ab7 |
A |
T |
7: 102,978,115 (GRCm39) |
I141F |
possibly damaging |
Het |
Or8b12c |
A |
G |
9: 37,715,317 (GRCm39) |
T37A |
probably benign |
Het |
Parl |
G |
A |
16: 20,120,963 (GRCm39) |
R39C |
possibly damaging |
Het |
Pcdha9 |
G |
A |
18: 37,132,028 (GRCm39) |
V366I |
probably benign |
Het |
Pdzd8 |
A |
G |
19: 59,288,994 (GRCm39) |
V802A |
probably benign |
Het |
Plcl2 |
T |
C |
17: 50,913,873 (GRCm39) |
V294A |
probably damaging |
Het |
Plxna2 |
T |
A |
1: 194,472,504 (GRCm39) |
S1083T |
probably benign |
Het |
Polr2a |
G |
T |
11: 69,638,047 (GRCm39) |
L141I |
possibly damaging |
Het |
Ptpre |
C |
A |
7: 135,272,909 (GRCm39) |
R468S |
probably damaging |
Het |
Raet1e |
T |
A |
10: 22,056,770 (GRCm39) |
N115K |
probably benign |
Het |
Rfx8 |
C |
A |
1: 39,709,554 (GRCm39) |
S491I |
probably damaging |
Het |
Rpe |
T |
A |
1: 66,740,807 (GRCm39) |
L48* |
probably null |
Het |
Skint5 |
A |
T |
4: 113,800,064 (GRCm39) |
|
probably null |
Het |
Spata24 |
C |
A |
18: 35,793,389 (GRCm39) |
S111I |
possibly damaging |
Het |
Suz12 |
G |
C |
11: 79,893,006 (GRCm39) |
|
probably benign |
Het |
Taf4 |
T |
A |
2: 179,573,832 (GRCm39) |
I679F |
probably damaging |
Het |
Tlr1 |
G |
T |
5: 65,084,472 (GRCm39) |
P35Q |
possibly damaging |
Het |
Tonsl |
T |
C |
15: 76,520,418 (GRCm39) |
|
probably null |
Het |
Tsen54 |
G |
A |
11: 115,711,513 (GRCm39) |
R310H |
probably benign |
Het |
Ttc7b |
A |
G |
12: 100,461,681 (GRCm39) |
S99P |
probably benign |
Het |
Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
Uhmk1 |
T |
A |
1: 170,027,563 (GRCm39) |
N378I |
probably damaging |
Het |
Vmn2r107 |
A |
G |
17: 20,565,849 (GRCm39) |
T55A |
probably benign |
Het |
Vmn2r74 |
C |
T |
7: 85,601,280 (GRCm39) |
C786Y |
probably damaging |
Het |
Wdr20rt |
C |
T |
12: 65,272,964 (GRCm39) |
|
probably benign |
Het |
Zfand2a |
T |
A |
5: 139,467,746 (GRCm39) |
H42L |
probably damaging |
Het |
Zfp990 |
T |
A |
4: 145,264,483 (GRCm39) |
C494S |
probably damaging |
Het |
|
Other mutations in Zkscan4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01353:Zkscan4
|
APN |
13 |
21,668,518 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01358:Zkscan4
|
APN |
13 |
21,668,475 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0107:Zkscan4
|
UTSW |
13 |
21,668,751 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0637:Zkscan4
|
UTSW |
13 |
21,665,477 (GRCm39) |
missense |
probably damaging |
0.99 |
R0791:Zkscan4
|
UTSW |
13 |
21,668,081 (GRCm39) |
missense |
probably benign |
0.04 |
R1252:Zkscan4
|
UTSW |
13 |
21,668,044 (GRCm39) |
missense |
probably benign |
0.02 |
R1870:Zkscan4
|
UTSW |
13 |
21,668,104 (GRCm39) |
missense |
probably benign |
0.00 |
R4771:Zkscan4
|
UTSW |
13 |
21,663,416 (GRCm39) |
nonsense |
probably null |
|
R5080:Zkscan4
|
UTSW |
13 |
21,665,498 (GRCm39) |
missense |
probably benign |
0.02 |
R5987:Zkscan4
|
UTSW |
13 |
21,668,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R6542:Zkscan4
|
UTSW |
13 |
21,668,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R6954:Zkscan4
|
UTSW |
13 |
21,668,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R7227:Zkscan4
|
UTSW |
13 |
21,668,413 (GRCm39) |
missense |
probably benign |
0.00 |
R7418:Zkscan4
|
UTSW |
13 |
21,668,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R7462:Zkscan4
|
UTSW |
13 |
21,668,044 (GRCm39) |
missense |
probably benign |
0.02 |
R7549:Zkscan4
|
UTSW |
13 |
21,668,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R7750:Zkscan4
|
UTSW |
13 |
21,663,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R8051:Zkscan4
|
UTSW |
13 |
21,668,823 (GRCm39) |
missense |
not run |
|
R8942:Zkscan4
|
UTSW |
13 |
21,668,680 (GRCm39) |
missense |
probably benign |
0.00 |
R9040:Zkscan4
|
UTSW |
13 |
21,668,229 (GRCm39) |
missense |
probably benign |
|
R9297:Zkscan4
|
UTSW |
13 |
21,668,201 (GRCm39) |
missense |
probably benign |
0.06 |
R9304:Zkscan4
|
UTSW |
13 |
21,665,570 (GRCm39) |
missense |
possibly damaging |
0.75 |
RF049:Zkscan4
|
UTSW |
13 |
21,668,881 (GRCm39) |
frame shift |
probably null |
|
T0722:Zkscan4
|
UTSW |
13 |
21,663,370 (GRCm39) |
small deletion |
probably benign |
|
T0975:Zkscan4
|
UTSW |
13 |
21,663,370 (GRCm39) |
small deletion |
probably benign |
|
Z1088:Zkscan4
|
UTSW |
13 |
21,668,067 (GRCm39) |
missense |
probably damaging |
1.00 |
|