Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aco1 |
T |
G |
4: 40,175,730 (GRCm39) |
L157R |
probably damaging |
Het |
Acot11 |
A |
T |
4: 106,606,550 (GRCm39) |
L513Q |
probably damaging |
Het |
Amd1 |
A |
G |
10: 40,170,755 (GRCm39) |
I52T |
probably benign |
Het |
Ap2b1 |
T |
C |
11: 83,237,721 (GRCm39) |
I557T |
probably benign |
Het |
Arel1 |
T |
A |
12: 84,987,173 (GRCm39) |
|
probably null |
Het |
Arg1 |
T |
A |
10: 24,792,762 (GRCm39) |
|
probably null |
Het |
Atf1 |
A |
T |
15: 100,152,052 (GRCm39) |
M135L |
probably benign |
Het |
Atf2 |
T |
C |
2: 73,681,242 (GRCm39) |
E77G |
possibly damaging |
Het |
Axin1 |
G |
T |
17: 26,403,199 (GRCm39) |
A394S |
probably damaging |
Het |
Axin1 |
A |
T |
17: 26,409,202 (GRCm39) |
Q734L |
probably damaging |
Het |
Brd8 |
G |
C |
18: 34,735,819 (GRCm39) |
A886G |
probably damaging |
Het |
Ccdc39 |
T |
C |
3: 33,880,629 (GRCm39) |
K446R |
probably damaging |
Het |
Celf3 |
T |
C |
3: 94,392,634 (GRCm39) |
V35A |
probably damaging |
Het |
Cfap299 |
T |
A |
5: 98,494,093 (GRCm39) |
D32E |
probably damaging |
Het |
Ckap2 |
T |
C |
8: 22,665,803 (GRCm39) |
T415A |
possibly damaging |
Het |
Crybg3 |
T |
C |
16: 59,323,600 (GRCm39) |
Y1066C |
probably damaging |
Het |
Csmd3 |
T |
C |
15: 47,713,144 (GRCm39) |
H1506R |
probably benign |
Het |
Dnah10 |
A |
G |
5: 124,852,267 (GRCm39) |
D1808G |
probably damaging |
Het |
Dsc3 |
C |
T |
18: 20,113,729 (GRCm39) |
G398R |
probably damaging |
Het |
Emc2 |
A |
G |
15: 43,390,863 (GRCm39) |
Q293R |
probably damaging |
Het |
Fam151a |
A |
T |
4: 106,591,112 (GRCm39) |
|
probably benign |
Het |
Fbxw16 |
T |
A |
9: 109,270,289 (GRCm39) |
I151F |
probably damaging |
Het |
Fmnl2 |
A |
G |
2: 53,004,880 (GRCm39) |
D658G |
probably damaging |
Het |
Fnip2 |
G |
A |
3: 79,400,779 (GRCm39) |
T314I |
probably benign |
Het |
Foxc2 |
T |
A |
8: 121,843,413 (GRCm39) |
S20R |
probably damaging |
Het |
Fpr-rs6 |
C |
T |
17: 20,402,918 (GRCm39) |
G148R |
probably damaging |
Het |
Fsip2 |
T |
C |
2: 82,823,124 (GRCm39) |
S6286P |
possibly damaging |
Het |
Fyb2 |
A |
T |
4: 104,770,846 (GRCm39) |
I54F |
probably benign |
Het |
Gbf1 |
T |
C |
19: 46,260,003 (GRCm39) |
F999L |
probably damaging |
Het |
Gldc |
G |
A |
19: 30,114,513 (GRCm39) |
R466* |
probably null |
Het |
Gm12695 |
T |
A |
4: 96,651,082 (GRCm39) |
S124C |
probably benign |
Het |
Gm4846 |
A |
T |
1: 166,314,533 (GRCm39) |
I370N |
possibly damaging |
Het |
Gsdmc3 |
T |
C |
15: 63,730,296 (GRCm39) |
T423A |
probably damaging |
Het |
Hjurp |
GT |
GTT |
1: 88,194,246 (GRCm39) |
|
probably null |
Het |
Jarid2 |
T |
A |
13: 45,059,752 (GRCm39) |
N661K |
probably damaging |
Het |
Kcnmb3 |
T |
C |
3: 32,526,492 (GRCm39) |
Y233C |
probably damaging |
Het |
Kidins220 |
A |
G |
12: 25,044,905 (GRCm39) |
D191G |
probably damaging |
Het |
Kmt2a |
A |
G |
9: 44,732,757 (GRCm39) |
|
probably benign |
Het |
Krt1 |
T |
C |
15: 101,757,427 (GRCm39) |
D261G |
probably benign |
Het |
Lrba |
A |
G |
3: 86,513,175 (GRCm39) |
|
probably null |
Het |
Myo1f |
C |
T |
17: 33,817,146 (GRCm39) |
R730* |
probably null |
Het |
Ncoa7 |
C |
A |
10: 30,530,426 (GRCm39) |
E30* |
probably null |
Het |
Neurod4 |
T |
A |
10: 130,106,918 (GRCm39) |
K119* |
probably null |
Het |
Npy5r |
T |
C |
8: 67,133,929 (GRCm39) |
D288G |
probably benign |
Het |
Nr3c2 |
A |
T |
8: 77,636,092 (GRCm39) |
I398L |
probably damaging |
Het |
Or10a5 |
T |
C |
7: 106,635,565 (GRCm39) |
S68P |
probably damaging |
Het |
Or12j4 |
C |
A |
7: 140,046,574 (GRCm39) |
F153L |
probably benign |
Het |
Or4b1 |
T |
C |
2: 89,979,748 (GRCm39) |
S201G |
probably damaging |
Het |
Or4k35 |
T |
C |
2: 111,099,938 (GRCm39) |
Y258C |
probably damaging |
Het |
Or51v8 |
A |
T |
7: 103,320,103 (GRCm39) |
I45N |
probably damaging |
Het |
Or5g25 |
T |
C |
2: 85,478,090 (GRCm39) |
T192A |
possibly damaging |
Het |
Or5w8 |
A |
G |
2: 87,687,759 (GRCm39) |
K80R |
probably benign |
Het |
Or9m1b |
A |
G |
2: 87,836,648 (GRCm39) |
F149S |
probably damaging |
Het |
P3r3urf |
G |
A |
4: 116,031,376 (GRCm39) |
C82Y |
probably damaging |
Het |
Pcf11 |
A |
T |
7: 92,310,809 (GRCm39) |
M393K |
probably benign |
Het |
Pck2 |
T |
C |
14: 55,779,964 (GRCm39) |
V71A |
probably benign |
Het |
Pdzd8 |
G |
T |
19: 59,288,554 (GRCm39) |
L949I |
probably benign |
Het |
Pdzrn4 |
G |
A |
15: 92,644,190 (GRCm39) |
|
probably null |
Het |
Phospho1 |
A |
G |
11: 95,721,705 (GRCm39) |
N125S |
probably damaging |
Het |
Pirb |
A |
T |
7: 3,720,637 (GRCm39) |
L287Q |
probably benign |
Het |
Ppid |
A |
T |
3: 79,509,606 (GRCm39) |
K308* |
probably null |
Het |
Ppp1r1b |
A |
G |
11: 98,246,189 (GRCm39) |
E57G |
probably damaging |
Het |
Prtg |
T |
G |
9: 72,755,604 (GRCm39) |
S269A |
probably benign |
Het |
Rbbp5 |
T |
A |
1: 132,422,035 (GRCm39) |
S312T |
probably damaging |
Het |
Rbm11 |
T |
A |
16: 75,395,656 (GRCm39) |
|
probably null |
Het |
Retreg1 |
A |
G |
15: 25,970,250 (GRCm39) |
T139A |
probably damaging |
Het |
Riok3 |
T |
A |
18: 12,270,019 (GRCm39) |
H120Q |
probably damaging |
Het |
Rln1 |
A |
T |
19: 29,311,995 (GRCm39) |
M1K |
probably null |
Het |
Rpp30 |
C |
T |
19: 36,066,549 (GRCm39) |
S94L |
probably damaging |
Het |
Sccpdh |
C |
T |
1: 179,511,879 (GRCm39) |
P117L |
probably damaging |
Het |
Serac1 |
T |
C |
17: 6,099,274 (GRCm39) |
K506E |
possibly damaging |
Het |
Serping1 |
G |
T |
2: 84,596,072 (GRCm39) |
T454K |
probably damaging |
Het |
Slc1a2 |
T |
A |
2: 102,570,245 (GRCm39) |
N174K |
probably damaging |
Het |
Slc2a2 |
A |
G |
3: 28,773,634 (GRCm39) |
Q313R |
probably damaging |
Het |
Slc46a2 |
T |
A |
4: 59,914,249 (GRCm39) |
S225C |
probably damaging |
Het |
Smarcc2 |
G |
A |
10: 128,310,627 (GRCm39) |
E419K |
probably damaging |
Het |
Stkld1 |
T |
A |
2: 26,836,744 (GRCm39) |
|
probably null |
Het |
Szt2 |
A |
G |
4: 118,241,162 (GRCm39) |
M1704T |
probably benign |
Het |
Tasor |
T |
G |
14: 27,164,511 (GRCm39) |
C272W |
probably damaging |
Het |
Tfcp2l1 |
C |
T |
1: 118,580,653 (GRCm39) |
Q116* |
probably null |
Het |
Timm44 |
A |
G |
8: 4,310,603 (GRCm39) |
M383T |
possibly damaging |
Het |
Tnpo2 |
G |
A |
8: 85,771,946 (GRCm39) |
|
probably null |
Het |
Tnrc6b |
A |
G |
15: 80,764,640 (GRCm39) |
K714R |
probably damaging |
Het |
Wdfy3 |
A |
G |
5: 102,099,178 (GRCm39) |
L290P |
probably damaging |
Het |
Wdr59 |
A |
G |
8: 112,177,709 (GRCm39) |
F898L |
probably damaging |
Het |
Zfp120 |
A |
T |
2: 149,959,318 (GRCm39) |
C335S |
probably damaging |
Het |
Zfp518a |
T |
C |
19: 40,901,954 (GRCm39) |
S628P |
probably benign |
Het |
Zfp879 |
A |
T |
11: 50,724,355 (GRCm39) |
C234S |
probably damaging |
Het |
|
Other mutations in Evc2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00663:Evc2
|
APN |
5 |
37,579,235 (GRCm39) |
missense |
probably benign |
0.26 |
IGL01294:Evc2
|
APN |
5 |
37,504,854 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01547:Evc2
|
APN |
5 |
37,550,431 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02233:Evc2
|
APN |
5 |
37,535,681 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02253:Evc2
|
APN |
5 |
37,535,771 (GRCm39) |
splice site |
probably benign |
|
IGL02993:Evc2
|
APN |
5 |
37,576,501 (GRCm39) |
missense |
probably benign |
0.01 |
R0010:Evc2
|
UTSW |
5 |
37,574,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R0010:Evc2
|
UTSW |
5 |
37,574,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R0324:Evc2
|
UTSW |
5 |
37,550,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R0441:Evc2
|
UTSW |
5 |
37,574,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R0454:Evc2
|
UTSW |
5 |
37,574,828 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1291:Evc2
|
UTSW |
5 |
37,544,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R1433:Evc2
|
UTSW |
5 |
37,550,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R1485:Evc2
|
UTSW |
5 |
37,527,900 (GRCm39) |
missense |
probably benign |
0.30 |
R1491:Evc2
|
UTSW |
5 |
37,550,541 (GRCm39) |
critical splice donor site |
probably null |
|
R1502:Evc2
|
UTSW |
5 |
37,550,440 (GRCm39) |
missense |
probably benign |
|
R1662:Evc2
|
UTSW |
5 |
37,506,094 (GRCm39) |
missense |
probably benign |
0.00 |
R1891:Evc2
|
UTSW |
5 |
37,549,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R1983:Evc2
|
UTSW |
5 |
37,573,275 (GRCm39) |
nonsense |
probably null |
|
R2160:Evc2
|
UTSW |
5 |
37,537,862 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2237:Evc2
|
UTSW |
5 |
37,535,527 (GRCm39) |
missense |
probably benign |
0.22 |
R3926:Evc2
|
UTSW |
5 |
37,540,574 (GRCm39) |
missense |
probably damaging |
1.00 |
R3953:Evc2
|
UTSW |
5 |
37,537,931 (GRCm39) |
critical splice donor site |
probably null |
|
R3959:Evc2
|
UTSW |
5 |
37,573,120 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4281:Evc2
|
UTSW |
5 |
37,495,938 (GRCm39) |
missense |
probably benign |
0.33 |
R4366:Evc2
|
UTSW |
5 |
37,496,013 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4707:Evc2
|
UTSW |
5 |
37,579,204 (GRCm39) |
missense |
probably benign |
0.08 |
R4754:Evc2
|
UTSW |
5 |
37,544,375 (GRCm39) |
missense |
probably damaging |
0.99 |
R5373:Evc2
|
UTSW |
5 |
37,535,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R5593:Evc2
|
UTSW |
5 |
37,544,321 (GRCm39) |
missense |
probably damaging |
0.99 |
R5697:Evc2
|
UTSW |
5 |
37,527,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R5847:Evc2
|
UTSW |
5 |
37,562,068 (GRCm39) |
intron |
probably benign |
|
R5874:Evc2
|
UTSW |
5 |
37,574,883 (GRCm39) |
intron |
probably benign |
|
R6023:Evc2
|
UTSW |
5 |
37,505,960 (GRCm39) |
missense |
probably benign |
0.13 |
R6285:Evc2
|
UTSW |
5 |
37,581,923 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6394:Evc2
|
UTSW |
5 |
37,535,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R6567:Evc2
|
UTSW |
5 |
37,576,508 (GRCm39) |
missense |
probably benign |
0.17 |
R6669:Evc2
|
UTSW |
5 |
37,535,722 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7039:Evc2
|
UTSW |
5 |
37,579,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R7131:Evc2
|
UTSW |
5 |
37,567,602 (GRCm39) |
missense |
probably damaging |
1.00 |
R7144:Evc2
|
UTSW |
5 |
37,544,183 (GRCm39) |
missense |
probably damaging |
0.97 |
R7372:Evc2
|
UTSW |
5 |
37,544,477 (GRCm39) |
missense |
probably damaging |
0.98 |
R7376:Evc2
|
UTSW |
5 |
37,527,983 (GRCm39) |
missense |
possibly damaging |
0.57 |
R7607:Evc2
|
UTSW |
5 |
37,544,200 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7915:Evc2
|
UTSW |
5 |
37,544,206 (GRCm39) |
missense |
probably damaging |
0.98 |
R8144:Evc2
|
UTSW |
5 |
37,537,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R8506:Evc2
|
UTSW |
5 |
37,540,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R9097:Evc2
|
UTSW |
5 |
37,550,505 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9151:Evc2
|
UTSW |
5 |
37,504,823 (GRCm39) |
missense |
probably benign |
0.00 |
R9261:Evc2
|
UTSW |
5 |
37,537,895 (GRCm39) |
missense |
probably benign |
0.00 |
R9612:Evc2
|
UTSW |
5 |
37,544,130 (GRCm39) |
missense |
probably benign |
0.00 |
|