Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
A |
T |
3: 138,066,759 (GRCm38) |
K570* |
probably null |
Het |
Abi1 |
T |
C |
2: 22,971,250 (GRCm38) |
I99V |
probably damaging |
Het |
Abtb3 |
G |
A |
10: 85,388,094 (GRCm38) |
G256R |
unknown |
Het |
Adgrg7 |
T |
A |
16: 56,752,399 (GRCm38) |
E351D |
probably benign |
Het |
Ankrd34c |
T |
G |
9: 89,730,090 (GRCm38) |
K66T |
probably damaging |
Het |
Asap2 |
C |
T |
12: 21,112,143 (GRCm38) |
R34W |
probably damaging |
Het |
Atr |
A |
G |
9: 95,905,760 (GRCm38) |
T1469A |
probably benign |
Het |
Ccdc168 |
T |
C |
1: 44,057,124 (GRCm38) |
I1605V |
probably benign |
Het |
Celsr1 |
G |
T |
15: 85,937,993 (GRCm38) |
R1708S |
probably benign |
Het |
Chmp2a |
T |
A |
7: 13,033,913 (GRCm38) |
E28D |
probably benign |
Het |
Cldn24 |
A |
T |
8: 47,822,246 (GRCm38) |
N35I |
probably benign |
Het |
Coa6 |
G |
C |
8: 126,422,831 (GRCm38) |
|
probably null |
Het |
Copa |
C |
T |
1: 172,119,251 (GRCm38) |
R1009C |
probably damaging |
Het |
Crybb2 |
G |
A |
5: 113,062,047 (GRCm38) |
T150M |
possibly damaging |
Het |
Ctnnd2 |
A |
T |
15: 30,619,930 (GRCm38) |
T143S |
probably benign |
Het |
Eid3 |
A |
G |
10: 82,867,158 (GRCm38) |
N151S |
probably damaging |
Het |
Fbxo17 |
G |
T |
7: 28,735,308 (GRCm38) |
V173L |
possibly damaging |
Het |
Fmn2 |
CCCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATATCTCCCCTACCTCCTCTCCCTGGAATGGGAATACCTCC |
CCCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATATCTCCCCTACCTCCTCTCCCTGGAATGGGAATACCTCC |
1: 174,609,203 (GRCm38) |
|
probably benign |
Het |
Galntl6 |
T |
C |
8: 57,962,399 (GRCm38) |
N240S |
probably damaging |
Het |
Gck |
G |
T |
11: 5,901,733 (GRCm38) |
S445R |
probably damaging |
Het |
Gm5114 |
C |
A |
7: 39,408,294 (GRCm38) |
V634F |
probably benign |
Het |
Gnat2 |
G |
A |
3: 108,098,318 (GRCm38) |
D200N |
|
Het |
H13 |
A |
G |
2: 152,704,129 (GRCm38) |
N390S |
probably benign |
Het |
Helz |
T |
A |
11: 107,662,016 (GRCm38) |
M1206K |
probably damaging |
Het |
Itpr3 |
G |
A |
17: 27,118,677 (GRCm38) |
|
probably benign |
Het |
Kank1 |
G |
A |
19: 25,410,075 (GRCm38) |
G371R |
probably benign |
Het |
Kif13b |
A |
G |
14: 64,744,877 (GRCm38) |
T513A |
probably damaging |
Het |
L3mbtl4 |
T |
C |
17: 68,455,786 (GRCm38) |
S105P |
possibly damaging |
Het |
Lpo |
T |
A |
11: 87,807,022 (GRCm38) |
E653V |
probably benign |
Het |
Lyst |
A |
G |
13: 13,712,850 (GRCm38) |
D3088G |
possibly damaging |
Het |
Man2b1 |
C |
A |
8: 85,084,455 (GRCm38) |
H72N |
probably damaging |
Het |
Mast3 |
A |
T |
8: 70,781,157 (GRCm38) |
H981Q |
probably damaging |
Het |
Mul1 |
A |
C |
4: 138,434,853 (GRCm38) |
K32Q |
probably benign |
Het |
Oas1c |
C |
T |
5: 120,808,061 (GRCm38) |
S124N |
probably benign |
Het |
Omg |
T |
A |
11: 79,503,003 (GRCm38) |
K10* |
probably null |
Het |
Or2a52 |
A |
G |
6: 43,167,816 (GRCm38) |
I253V |
probably benign |
Het |
Or4k52 |
A |
T |
2: 111,780,841 (GRCm38) |
I174F |
probably damaging |
Het |
Or6c88 |
A |
G |
10: 129,571,177 (GRCm38) |
H174R |
probably damaging |
Het |
Pcdhb14 |
T |
A |
18: 37,449,639 (GRCm38) |
N599K |
probably damaging |
Het |
Pcdhb18 |
C |
A |
18: 37,490,647 (GRCm38) |
N343K |
probably damaging |
Het |
Phf7 |
C |
A |
14: 31,249,656 (GRCm38) |
|
probably benign |
Het |
Pramel15 |
C |
T |
4: 144,372,827 (GRCm38) |
C456Y |
probably damaging |
Het |
Qdpr |
T |
C |
5: 45,447,640 (GRCm38) |
N42S |
probably damaging |
Het |
Rbm44 |
T |
A |
1: 91,162,414 (GRCm38) |
D716E |
probably benign |
Het |
Rprd2 |
A |
C |
3: 95,764,055 (GRCm38) |
H1345Q |
possibly damaging |
Het |
Rsf1 |
G |
GACGGCGGCT |
7: 97,579,909 (GRCm38) |
|
probably benign |
Het |
Ryr2 |
G |
A |
13: 11,799,882 (GRCm38) |
A668V |
probably damaging |
Het |
Sag |
T |
A |
1: 87,831,961 (GRCm38) |
L307Q |
probably damaging |
Het |
Sash1 |
G |
A |
10: 8,727,970 (GRCm38) |
P1106L |
probably damaging |
Het |
Sec16b |
T |
A |
1: 157,554,839 (GRCm38) |
I615N |
probably damaging |
Het |
Sfi1 |
A |
ATCTTCCCAAAGCCAGTGC |
11: 3,153,384 (GRCm38) |
|
probably benign |
Het |
Slco1b2 |
T |
C |
6: 141,683,267 (GRCm38) |
V600A |
probably benign |
Het |
Sucnr1 |
A |
G |
3: 60,086,842 (GRCm38) |
T264A |
probably benign |
Het |
Tbx3 |
A |
G |
5: 119,671,918 (GRCm38) |
|
probably benign |
Het |
Tigd5 |
T |
C |
15: 75,911,220 (GRCm38) |
V477A |
possibly damaging |
Het |
Tle7 |
T |
A |
8: 110,110,131 (GRCm38) |
S216R |
possibly damaging |
Het |
Ttc17 |
G |
A |
2: 94,362,419 (GRCm38) |
A89V |
probably damaging |
Het |
Twsg1 |
A |
G |
17: 65,948,662 (GRCm38) |
I39T |
|
Het |
Zfp184 |
T |
C |
13: 21,959,342 (GRCm38) |
F406S |
probably damaging |
Het |
Zfp429 |
A |
T |
13: 67,390,711 (GRCm38) |
C205S |
probably damaging |
Het |
Zfp59 |
T |
A |
7: 27,854,888 (GRCm38) |
D588E |
probably benign |
Het |
Zfp64 |
A |
T |
2: 168,955,163 (GRCm38) |
M1K |
probably null |
Het |
|
Other mutations in Meioc |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01391:Meioc
|
APN |
11 |
102,674,287 (GRCm38) |
missense |
probably benign |
0.33 |
IGL01952:Meioc
|
APN |
11 |
102,672,185 (GRCm38) |
missense |
possibly damaging |
0.79 |
IGL02006:Meioc
|
APN |
11 |
102,674,266 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02195:Meioc
|
APN |
11 |
102,674,857 (GRCm38) |
missense |
possibly damaging |
0.91 |
IGL02339:Meioc
|
APN |
11 |
102,668,448 (GRCm38) |
missense |
probably benign |
0.18 |
IGL02935:Meioc
|
APN |
11 |
102,672,191 (GRCm38) |
missense |
probably benign |
0.06 |
IGL03294:Meioc
|
APN |
11 |
102,680,669 (GRCm38) |
missense |
probably damaging |
1.00 |
PIT4519001:Meioc
|
UTSW |
11 |
102,679,957 (GRCm38) |
missense |
probably damaging |
1.00 |
R0285:Meioc
|
UTSW |
11 |
102,672,191 (GRCm38) |
missense |
probably benign |
0.06 |
R0964:Meioc
|
UTSW |
11 |
102,680,031 (GRCm38) |
missense |
probably damaging |
1.00 |
R1074:Meioc
|
UTSW |
11 |
102,675,393 (GRCm38) |
missense |
probably damaging |
1.00 |
R2024:Meioc
|
UTSW |
11 |
102,675,358 (GRCm38) |
missense |
probably benign |
0.00 |
R4012:Meioc
|
UTSW |
11 |
102,675,828 (GRCm38) |
missense |
probably damaging |
0.99 |
R4429:Meioc
|
UTSW |
11 |
102,675,720 (GRCm38) |
missense |
probably damaging |
1.00 |
R4491:Meioc
|
UTSW |
11 |
102,674,920 (GRCm38) |
missense |
possibly damaging |
0.84 |
R4594:Meioc
|
UTSW |
11 |
102,674,166 (GRCm38) |
missense |
probably damaging |
1.00 |
R4752:Meioc
|
UTSW |
11 |
102,674,433 (GRCm38) |
missense |
probably benign |
0.00 |
R5301:Meioc
|
UTSW |
11 |
102,680,045 (GRCm38) |
missense |
probably damaging |
1.00 |
R5352:Meioc
|
UTSW |
11 |
102,675,313 (GRCm38) |
missense |
probably benign |
0.03 |
R5646:Meioc
|
UTSW |
11 |
102,675,257 (GRCm38) |
missense |
possibly damaging |
0.94 |
R5958:Meioc
|
UTSW |
11 |
102,675,153 (GRCm38) |
missense |
probably benign |
0.41 |
R5968:Meioc
|
UTSW |
11 |
102,675,831 (GRCm38) |
missense |
probably damaging |
0.99 |
R6157:Meioc
|
UTSW |
11 |
102,668,401 (GRCm38) |
missense |
probably damaging |
1.00 |
R6410:Meioc
|
UTSW |
11 |
102,675,034 (GRCm38) |
missense |
probably benign |
0.00 |
R6644:Meioc
|
UTSW |
11 |
102,668,460 (GRCm38) |
critical splice donor site |
probably null |
|
R7285:Meioc
|
UTSW |
11 |
102,666,342 (GRCm38) |
missense |
probably benign |
0.00 |
R7440:Meioc
|
UTSW |
11 |
102,674,237 (GRCm38) |
missense |
possibly damaging |
0.67 |
R7815:Meioc
|
UTSW |
11 |
102,675,588 (GRCm38) |
missense |
probably damaging |
1.00 |
R7984:Meioc
|
UTSW |
11 |
102,674,606 (GRCm38) |
missense |
possibly damaging |
0.94 |
R8009:Meioc
|
UTSW |
11 |
102,676,743 (GRCm38) |
missense |
probably damaging |
1.00 |
R8078:Meioc
|
UTSW |
11 |
102,668,400 (GRCm38) |
nonsense |
probably null |
|
R8195:Meioc
|
UTSW |
11 |
102,675,067 (GRCm38) |
nonsense |
probably null |
|
R8429:Meioc
|
UTSW |
11 |
102,674,206 (GRCm38) |
missense |
probably benign |
0.06 |
R8797:Meioc
|
UTSW |
11 |
102,676,860 (GRCm38) |
nonsense |
probably null |
|
R8854:Meioc
|
UTSW |
11 |
102,675,763 (GRCm38) |
missense |
probably damaging |
0.98 |
R9081:Meioc
|
UTSW |
11 |
102,674,175 (GRCm38) |
missense |
probably benign |
0.00 |
R9360:Meioc
|
UTSW |
11 |
102,674,953 (GRCm38) |
missense |
probably benign |
0.13 |
R9539:Meioc
|
UTSW |
11 |
102,674,680 (GRCm38) |
missense |
probably damaging |
0.99 |
R9549:Meioc
|
UTSW |
11 |
102,665,724 (GRCm38) |
intron |
probably benign |
|
R9751:Meioc
|
UTSW |
11 |
102,675,593 (GRCm38) |
nonsense |
probably null |
|
Z1177:Meioc
|
UTSW |
11 |
102,666,364 (GRCm38) |
frame shift |
probably null |
|
|