Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc9 |
A |
G |
6: 142,571,678 (GRCm39) |
F1137S |
probably damaging |
Het |
Actr6 |
G |
T |
10: 89,564,054 (GRCm39) |
Q73K |
probably benign |
Het |
Adamtsl3 |
G |
A |
7: 82,225,265 (GRCm39) |
G358D |
probably damaging |
Het |
Aggf1 |
A |
G |
13: 95,508,084 (GRCm39) |
V94A |
probably damaging |
Het |
Arpc3 |
A |
G |
5: 122,541,459 (GRCm39) |
Y57C |
probably damaging |
Het |
Asb2 |
A |
G |
12: 103,287,814 (GRCm39) |
Y630H |
probably benign |
Het |
Atp1a1 |
A |
T |
3: 101,497,090 (GRCm39) |
N405K |
probably benign |
Het |
C6 |
G |
T |
15: 4,837,996 (GRCm39) |
D869Y |
possibly damaging |
Het |
Cds2 |
A |
G |
2: 132,139,168 (GRCm39) |
Y137C |
probably damaging |
Het |
Ceacam12 |
A |
T |
7: 17,803,131 (GRCm39) |
E179V |
probably damaging |
Het |
Chgb |
T |
A |
2: 132,634,516 (GRCm39) |
Y153N |
probably benign |
Het |
Cit |
T |
A |
5: 116,135,593 (GRCm39) |
L1831Q |
probably damaging |
Het |
Cpne8 |
C |
A |
15: 90,373,191 (GRCm39) |
*578L |
probably null |
Het |
Cspg5 |
A |
G |
9: 110,080,151 (GRCm39) |
T440A |
probably damaging |
Het |
Dnah7a |
A |
C |
1: 53,598,467 (GRCm39) |
V1393G |
probably damaging |
Het |
Dnajb8 |
A |
G |
6: 88,199,575 (GRCm39) |
D37G |
probably benign |
Het |
Dst |
A |
G |
1: 34,213,273 (GRCm39) |
I1063M |
probably benign |
Het |
Efs |
T |
G |
14: 55,156,951 (GRCm39) |
|
probably null |
Het |
Gpatch1 |
A |
G |
7: 34,991,257 (GRCm39) |
S596P |
probably damaging |
Het |
Hbs1l |
C |
A |
10: 21,217,655 (GRCm39) |
H190Q |
probably benign |
Het |
Ighm |
A |
G |
12: 113,386,329 (GRCm39) |
V7A |
unknown |
Het |
Ivd |
A |
T |
2: 118,707,370 (GRCm39) |
I295F |
possibly damaging |
Het |
Kcnq5 |
A |
C |
1: 21,575,931 (GRCm39) |
S258A |
probably damaging |
Het |
Mad1l1 |
G |
T |
5: 140,247,334 (GRCm39) |
P331Q |
probably damaging |
Het |
Mcf2l |
G |
T |
8: 13,063,922 (GRCm39) |
G1045C |
probably damaging |
Het |
Mcoln1 |
T |
A |
8: 3,558,701 (GRCm39) |
I233N |
probably damaging |
Het |
Mmp13 |
T |
C |
9: 7,276,580 (GRCm39) |
L225P |
probably damaging |
Het |
Muc5ac |
G |
A |
7: 141,371,644 (GRCm39) |
C2615Y |
possibly damaging |
Het |
Myh7b |
T |
C |
2: 155,463,315 (GRCm39) |
F516L |
probably damaging |
Het |
Obsl1 |
A |
T |
1: 75,467,851 (GRCm39) |
S1347R |
probably damaging |
Het |
Ogn |
A |
G |
13: 49,771,761 (GRCm39) |
N207S |
probably benign |
Het |
Or2h15 |
C |
A |
17: 38,441,598 (GRCm39) |
A162S |
probably benign |
Het |
Or8b12 |
T |
A |
9: 37,658,330 (GRCm39) |
L300Q |
probably damaging |
Het |
Pcdha2 |
G |
T |
18: 37,074,159 (GRCm39) |
V597L |
probably damaging |
Het |
Pcnt |
T |
A |
10: 76,217,897 (GRCm39) |
Y2126F |
possibly damaging |
Het |
Pgbd5 |
A |
T |
8: 125,101,056 (GRCm39) |
M400K |
possibly damaging |
Het |
Pklr |
A |
T |
3: 89,043,503 (GRCm39) |
E5V |
probably benign |
Het |
Pkp4 |
T |
A |
2: 59,135,411 (GRCm39) |
D94E |
probably benign |
Het |
Ppan |
C |
T |
9: 20,800,969 (GRCm39) |
Q111* |
probably null |
Het |
Prkcb |
A |
G |
7: 122,143,926 (GRCm39) |
N330S |
probably benign |
Het |
Prl4a1 |
T |
A |
13: 28,202,499 (GRCm39) |
W25R |
probably damaging |
Het |
Rars2 |
T |
A |
4: 34,656,855 (GRCm39) |
H501Q |
possibly damaging |
Het |
Ryr2 |
T |
C |
13: 11,741,839 (GRCm39) |
D2114G |
probably damaging |
Het |
Serinc2 |
G |
T |
4: 130,149,314 (GRCm39) |
T351K |
possibly damaging |
Het |
Slc22a12 |
A |
G |
19: 6,587,881 (GRCm39) |
F358L |
probably damaging |
Het |
Sorcs2 |
A |
C |
5: 36,186,427 (GRCm39) |
V905G |
probably damaging |
Het |
Tekt3 |
G |
C |
11: 62,985,573 (GRCm39) |
A460P |
probably damaging |
Het |
Tm4sf1 |
T |
G |
3: 57,200,289 (GRCm39) |
I109L |
possibly damaging |
Het |
Tmc5 |
A |
T |
7: 118,269,948 (GRCm39) |
E899D |
probably damaging |
Het |
Tmem268 |
C |
T |
4: 63,486,746 (GRCm39) |
P90S |
probably damaging |
Het |
Trim38 |
A |
G |
13: 23,966,717 (GRCm39) |
M55V |
probably benign |
Het |
Trip10 |
T |
G |
17: 57,557,963 (GRCm39) |
V50G |
probably damaging |
Het |
Usp25 |
T |
A |
16: 76,911,942 (GRCm39) |
C990* |
probably null |
Het |
Uts2 |
A |
G |
4: 151,083,506 (GRCm39) |
D39G |
probably benign |
Het |
Vezf1 |
T |
A |
11: 87,964,560 (GRCm39) |
C49* |
probably null |
Het |
Yeats2 |
C |
A |
16: 20,026,513 (GRCm39) |
Y796* |
probably null |
Het |
Zfp592 |
G |
A |
7: 80,687,645 (GRCm39) |
G890D |
possibly damaging |
Het |
Zfp647 |
G |
A |
15: 76,796,285 (GRCm39) |
P125L |
probably damaging |
Het |
|
Other mutations in Wee2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00335:Wee2
|
APN |
6 |
40,438,995 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01096:Wee2
|
APN |
6 |
40,440,187 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01978:Wee2
|
APN |
6 |
40,432,087 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03026:Wee2
|
APN |
6 |
40,438,915 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03091:Wee2
|
APN |
6 |
40,438,968 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03350:Wee2
|
APN |
6 |
40,426,665 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03352:Wee2
|
APN |
6 |
40,429,589 (GRCm39) |
critical splice donor site |
probably null |
|
R0420:Wee2
|
UTSW |
6 |
40,433,929 (GRCm39) |
missense |
probably benign |
0.04 |
R0506:Wee2
|
UTSW |
6 |
40,440,187 (GRCm39) |
missense |
probably benign |
0.04 |
R1205:Wee2
|
UTSW |
6 |
40,420,875 (GRCm39) |
start gained |
probably benign |
|
R1702:Wee2
|
UTSW |
6 |
40,441,135 (GRCm39) |
missense |
probably benign |
0.04 |
R3982:Wee2
|
UTSW |
6 |
40,432,175 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3983:Wee2
|
UTSW |
6 |
40,432,175 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6020:Wee2
|
UTSW |
6 |
40,426,554 (GRCm39) |
splice site |
probably null |
|
R6127:Wee2
|
UTSW |
6 |
40,426,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R6189:Wee2
|
UTSW |
6 |
40,426,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R6342:Wee2
|
UTSW |
6 |
40,421,189 (GRCm39) |
missense |
probably benign |
0.05 |
R6347:Wee2
|
UTSW |
6 |
40,432,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R6350:Wee2
|
UTSW |
6 |
40,432,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R6513:Wee2
|
UTSW |
6 |
40,429,553 (GRCm39) |
missense |
probably benign |
0.00 |
R7091:Wee2
|
UTSW |
6 |
40,438,936 (GRCm39) |
missense |
probably benign |
0.00 |
R8258:Wee2
|
UTSW |
6 |
40,421,114 (GRCm39) |
missense |
probably benign |
0.00 |
R8259:Wee2
|
UTSW |
6 |
40,421,114 (GRCm39) |
missense |
probably benign |
0.00 |
R8463:Wee2
|
UTSW |
6 |
40,420,914 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R8853:Wee2
|
UTSW |
6 |
40,441,200 (GRCm39) |
missense |
probably benign |
0.07 |
R9028:Wee2
|
UTSW |
6 |
40,421,189 (GRCm39) |
missense |
probably benign |
|
R9170:Wee2
|
UTSW |
6 |
40,437,977 (GRCm39) |
missense |
probably benign |
0.07 |
R9231:Wee2
|
UTSW |
6 |
40,440,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R9394:Wee2
|
UTSW |
6 |
40,433,878 (GRCm39) |
missense |
probably damaging |
0.96 |
R9474:Wee2
|
UTSW |
6 |
40,432,044 (GRCm39) |
nonsense |
probably null |
|
R9493:Wee2
|
UTSW |
6 |
40,421,057 (GRCm39) |
missense |
probably benign |
0.39 |
|