Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
A |
T |
3: 137,772,520 (GRCm39) |
K570* |
probably null |
Het |
Abi1 |
T |
C |
2: 22,861,262 (GRCm39) |
I99V |
probably damaging |
Het |
Abtb3 |
G |
A |
10: 85,223,958 (GRCm39) |
G256R |
unknown |
Het |
Adgrg7 |
T |
A |
16: 56,572,762 (GRCm39) |
E351D |
probably benign |
Het |
Ankrd34c |
T |
G |
9: 89,612,143 (GRCm39) |
K66T |
probably damaging |
Het |
Asap2 |
C |
T |
12: 21,162,144 (GRCm39) |
R34W |
probably damaging |
Het |
Atr |
A |
G |
9: 95,787,813 (GRCm39) |
T1469A |
probably benign |
Het |
Ccdc168 |
T |
C |
1: 44,096,284 (GRCm39) |
I1605V |
probably benign |
Het |
Celsr1 |
G |
T |
15: 85,822,194 (GRCm39) |
R1708S |
probably benign |
Het |
Chmp2a |
T |
A |
7: 12,767,840 (GRCm39) |
E28D |
probably benign |
Het |
Cldn24 |
A |
T |
8: 48,275,281 (GRCm39) |
N35I |
probably benign |
Het |
Coa6 |
G |
C |
8: 127,149,570 (GRCm39) |
|
probably null |
Het |
Copa |
C |
T |
1: 171,946,818 (GRCm39) |
R1009C |
probably damaging |
Het |
Crybb2 |
G |
A |
5: 113,209,913 (GRCm39) |
T150M |
possibly damaging |
Het |
Ctnnd2 |
A |
T |
15: 30,620,076 (GRCm39) |
T143S |
probably benign |
Het |
Eid3 |
A |
G |
10: 82,702,992 (GRCm39) |
N151S |
probably damaging |
Het |
Fbxo17 |
G |
T |
7: 28,434,733 (GRCm39) |
V173L |
possibly damaging |
Het |
Fmn2 |
CCCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATATCTCCCCTACCTCCTCTCCCTGGAATGGGAATACCTCC |
CCCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATATCTCCCCTACCTCCTCTCCCTGGAATGGGAATACCTCC |
1: 174,436,769 (GRCm39) |
|
probably benign |
Het |
Galntl6 |
T |
C |
8: 58,415,433 (GRCm39) |
N240S |
probably damaging |
Het |
Gck |
G |
T |
11: 5,851,733 (GRCm39) |
S445R |
probably damaging |
Het |
Gm5114 |
C |
A |
7: 39,057,718 (GRCm39) |
V634F |
probably benign |
Het |
Gnat2 |
G |
A |
3: 108,005,634 (GRCm39) |
D200N |
|
Het |
H13 |
A |
G |
2: 152,546,049 (GRCm39) |
N390S |
probably benign |
Het |
Helz |
T |
A |
11: 107,552,842 (GRCm39) |
M1206K |
probably damaging |
Het |
Itpr3 |
G |
A |
17: 27,337,651 (GRCm39) |
|
probably benign |
Het |
Kank1 |
G |
A |
19: 25,387,439 (GRCm39) |
G371R |
probably benign |
Het |
Kif13b |
A |
G |
14: 64,982,326 (GRCm39) |
T513A |
probably damaging |
Het |
L3mbtl4 |
T |
C |
17: 68,762,781 (GRCm39) |
S105P |
possibly damaging |
Het |
Lyst |
A |
G |
13: 13,887,435 (GRCm39) |
D3088G |
possibly damaging |
Het |
Man2b1 |
C |
A |
8: 85,811,084 (GRCm39) |
H72N |
probably damaging |
Het |
Mast3 |
A |
T |
8: 71,233,801 (GRCm39) |
H981Q |
probably damaging |
Het |
Meioc |
T |
A |
11: 102,559,246 (GRCm39) |
I56N |
probably benign |
Het |
Mul1 |
A |
C |
4: 138,162,164 (GRCm39) |
K32Q |
probably benign |
Het |
Oas1c |
C |
T |
5: 120,946,126 (GRCm39) |
S124N |
probably benign |
Het |
Omg |
T |
A |
11: 79,393,829 (GRCm39) |
K10* |
probably null |
Het |
Or2a52 |
A |
G |
6: 43,144,750 (GRCm39) |
I253V |
probably benign |
Het |
Or4k52 |
A |
T |
2: 111,611,186 (GRCm39) |
I174F |
probably damaging |
Het |
Or6c88 |
A |
G |
10: 129,407,046 (GRCm39) |
H174R |
probably damaging |
Het |
Pcdhb14 |
T |
A |
18: 37,582,692 (GRCm39) |
N599K |
probably damaging |
Het |
Pcdhb18 |
C |
A |
18: 37,623,700 (GRCm39) |
N343K |
probably damaging |
Het |
Phf7 |
C |
A |
14: 30,971,613 (GRCm39) |
|
probably benign |
Het |
Pramel15 |
C |
T |
4: 144,099,397 (GRCm39) |
C456Y |
probably damaging |
Het |
Qdpr |
T |
C |
5: 45,604,982 (GRCm39) |
N42S |
probably damaging |
Het |
Rbm44 |
T |
A |
1: 91,090,136 (GRCm39) |
D716E |
probably benign |
Het |
Rprd2 |
A |
C |
3: 95,671,367 (GRCm39) |
H1345Q |
possibly damaging |
Het |
Rsf1 |
G |
GACGGCGGCT |
7: 97,229,116 (GRCm39) |
|
probably benign |
Het |
Ryr2 |
G |
A |
13: 11,814,768 (GRCm39) |
A668V |
probably damaging |
Het |
Sag |
T |
A |
1: 87,759,683 (GRCm39) |
L307Q |
probably damaging |
Het |
Sash1 |
G |
A |
10: 8,603,734 (GRCm39) |
P1106L |
probably damaging |
Het |
Sec16b |
T |
A |
1: 157,382,409 (GRCm39) |
I615N |
probably damaging |
Het |
Sfi1 |
A |
ATCTTCCCAAAGCCAGTGC |
11: 3,103,384 (GRCm39) |
|
probably benign |
Het |
Slco1b2 |
T |
C |
6: 141,628,993 (GRCm39) |
V600A |
probably benign |
Het |
Sucnr1 |
A |
G |
3: 59,994,263 (GRCm39) |
T264A |
probably benign |
Het |
Tbx3 |
A |
G |
5: 119,809,983 (GRCm39) |
|
probably benign |
Het |
Tigd5 |
T |
C |
15: 75,783,069 (GRCm39) |
V477A |
possibly damaging |
Het |
Tle7 |
T |
A |
8: 110,836,763 (GRCm39) |
S216R |
possibly damaging |
Het |
Ttc17 |
G |
A |
2: 94,192,764 (GRCm39) |
A89V |
probably damaging |
Het |
Twsg1 |
A |
G |
17: 66,255,657 (GRCm39) |
I39T |
|
Het |
Zfp184 |
T |
C |
13: 22,143,512 (GRCm39) |
F406S |
probably damaging |
Het |
Zfp429 |
A |
T |
13: 67,538,830 (GRCm39) |
C205S |
probably damaging |
Het |
Zfp59 |
T |
A |
7: 27,554,313 (GRCm39) |
D588E |
probably benign |
Het |
Zfp64 |
A |
T |
2: 168,797,083 (GRCm39) |
M1K |
probably null |
Het |
|
Other mutations in Lpo |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01483:Lpo
|
APN |
11 |
87,711,964 (GRCm39) |
missense |
probably benign |
0.43 |
IGL01833:Lpo
|
APN |
11 |
87,698,159 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL02413:Lpo
|
APN |
11 |
87,697,732 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02706:Lpo
|
APN |
11 |
87,708,599 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02865:Lpo
|
APN |
11 |
87,697,803 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02939:Lpo
|
APN |
11 |
87,706,004 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1072:Lpo
|
UTSW |
11 |
87,709,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R1169:Lpo
|
UTSW |
11 |
87,708,143 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1667:Lpo
|
UTSW |
11 |
87,698,067 (GRCm39) |
unclassified |
probably benign |
|
R1719:Lpo
|
UTSW |
11 |
87,700,018 (GRCm39) |
splice site |
probably null |
|
R2133:Lpo
|
UTSW |
11 |
87,711,956 (GRCm39) |
missense |
probably benign |
0.17 |
R2871:Lpo
|
UTSW |
11 |
87,707,350 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2871:Lpo
|
UTSW |
11 |
87,707,350 (GRCm39) |
missense |
possibly damaging |
0.51 |
R4382:Lpo
|
UTSW |
11 |
87,713,027 (GRCm39) |
missense |
probably benign |
0.14 |
R4657:Lpo
|
UTSW |
11 |
87,705,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R4936:Lpo
|
UTSW |
11 |
87,701,166 (GRCm39) |
missense |
probably benign |
0.02 |
R4969:Lpo
|
UTSW |
11 |
87,697,751 (GRCm39) |
missense |
probably benign |
0.09 |
R5368:Lpo
|
UTSW |
11 |
87,711,895 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5536:Lpo
|
UTSW |
11 |
87,707,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R6246:Lpo
|
UTSW |
11 |
87,713,058 (GRCm39) |
missense |
unknown |
|
R6556:Lpo
|
UTSW |
11 |
87,708,589 (GRCm39) |
nonsense |
probably null |
|
R6817:Lpo
|
UTSW |
11 |
87,700,067 (GRCm39) |
missense |
probably benign |
|
R7024:Lpo
|
UTSW |
11 |
87,707,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R7203:Lpo
|
UTSW |
11 |
87,700,077 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7206:Lpo
|
UTSW |
11 |
87,698,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R8355:Lpo
|
UTSW |
11 |
87,705,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R8455:Lpo
|
UTSW |
11 |
87,705,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R8693:Lpo
|
UTSW |
11 |
87,700,066 (GRCm39) |
missense |
probably benign |
0.04 |
R8848:Lpo
|
UTSW |
11 |
87,708,603 (GRCm39) |
missense |
probably benign |
0.00 |
R8989:Lpo
|
UTSW |
11 |
87,708,660 (GRCm39) |
missense |
probably benign |
0.00 |
RF010:Lpo
|
UTSW |
11 |
87,711,928 (GRCm39) |
missense |
probably benign |
0.00 |
|