Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700021P04Rik |
T |
G |
19: 24,043,366 (GRCm39) |
|
noncoding transcript |
Het |
a |
A |
T |
2: 154,887,678 (GRCm39) |
D46V |
probably damaging |
Het |
Aass |
A |
T |
6: 23,109,497 (GRCm39) |
D324E |
possibly damaging |
Het |
Abca12 |
G |
T |
1: 71,306,622 (GRCm39) |
T2028K |
possibly damaging |
Het |
Abt1 |
T |
C |
13: 23,606,316 (GRCm39) |
T213A |
probably benign |
Het |
Adcy1 |
A |
C |
11: 7,014,117 (GRCm39) |
Y173S |
probably damaging |
Het |
Aim2 |
T |
C |
1: 173,287,417 (GRCm39) |
|
probably null |
Het |
Akr1d1 |
G |
A |
6: 37,534,424 (GRCm39) |
V193M |
probably damaging |
Het |
Cars1 |
C |
T |
7: 143,123,234 (GRCm39) |
E461K |
probably damaging |
Het |
Ccdc80 |
T |
C |
16: 44,943,290 (GRCm39) |
L800P |
probably damaging |
Het |
Ccl22 |
A |
G |
8: 95,473,536 (GRCm39) |
Y27C |
probably damaging |
Het |
Cdc123 |
G |
A |
2: 5,815,566 (GRCm39) |
|
probably benign |
Het |
Cldn11 |
A |
T |
3: 31,217,278 (GRCm39) |
I149F |
probably benign |
Het |
Col14a1 |
T |
C |
15: 55,300,429 (GRCm39) |
Y986H |
unknown |
Het |
Col6a3 |
G |
A |
1: 90,749,605 (GRCm39) |
L410F |
probably damaging |
Het |
Crocc |
T |
C |
4: 140,761,282 (GRCm39) |
|
probably null |
Het |
Cubn |
A |
G |
2: 13,433,374 (GRCm39) |
|
probably benign |
Het |
Cwc25 |
G |
T |
11: 97,644,744 (GRCm39) |
Q205K |
probably benign |
Het |
Eps8l1 |
T |
A |
7: 4,473,797 (GRCm39) |
|
probably null |
Het |
Fasl |
C |
T |
1: 161,609,420 (GRCm39) |
V189M |
probably damaging |
Het |
Fbxw5 |
T |
C |
2: 25,394,643 (GRCm39) |
|
probably null |
Het |
Flg2 |
A |
C |
3: 93,110,828 (GRCm39) |
E952A |
unknown |
Het |
Gpd1l |
A |
T |
9: 114,746,146 (GRCm39) |
L90Q |
probably damaging |
Het |
Grik4 |
G |
T |
9: 42,509,180 (GRCm39) |
F414L |
probably benign |
Het |
Kcnh8 |
GAGACCAACGAGCAGCTGATGCTTCAGA |
GAGA |
17: 53,032,934 (GRCm39) |
74 |
probably benign |
Het |
Klhl3 |
C |
T |
13: 58,166,611 (GRCm39) |
G407S |
probably null |
Het |
Lmbr1 |
T |
C |
5: 29,463,753 (GRCm39) |
E157G |
probably damaging |
Het |
Lrp2 |
T |
A |
2: 69,343,617 (GRCm39) |
H914L |
probably damaging |
Het |
Mrpl20 |
A |
T |
4: 155,892,970 (GRCm39) |
D67V |
probably damaging |
Het |
Myo15a |
A |
G |
11: 60,378,022 (GRCm39) |
T1346A |
possibly damaging |
Het |
Naip5 |
A |
T |
13: 100,382,338 (GRCm39) |
C124S |
probably damaging |
Het |
Or10ag2 |
T |
A |
2: 87,248,801 (GRCm39) |
Y134* |
probably null |
Het |
Or13n4 |
T |
C |
7: 106,423,245 (GRCm39) |
T163A |
possibly damaging |
Het |
Or52u1 |
T |
A |
7: 104,237,830 (GRCm39) |
V290D |
probably damaging |
Het |
Osbp |
A |
G |
19: 11,956,030 (GRCm39) |
D385G |
probably benign |
Het |
Paip1 |
G |
A |
13: 119,593,540 (GRCm39) |
D460N |
probably damaging |
Het |
Pde3b |
T |
C |
7: 114,093,823 (GRCm39) |
S356P |
probably benign |
Het |
Pms2 |
A |
G |
5: 143,867,837 (GRCm39) |
M814V |
probably damaging |
Het |
Polg |
C |
A |
7: 79,114,576 (GRCm39) |
K128N |
probably damaging |
Het |
Polk |
G |
T |
13: 96,620,181 (GRCm39) |
T694K |
probably benign |
Het |
Pom121 |
T |
C |
5: 135,417,491 (GRCm39) |
K342R |
unknown |
Het |
Pou5f2 |
T |
C |
13: 78,174,024 (GRCm39) |
L322P |
probably damaging |
Het |
Prorp |
G |
T |
12: 55,351,398 (GRCm39) |
V236F |
possibly damaging |
Het |
Ptpn6 |
T |
C |
6: 124,705,382 (GRCm39) |
D183G |
probably damaging |
Het |
Pygb |
G |
A |
2: 150,668,391 (GRCm39) |
|
probably null |
Het |
Ralgds |
C |
T |
2: 28,442,283 (GRCm39) |
|
probably benign |
Het |
Ret |
T |
C |
6: 118,130,927 (GRCm39) |
T1079A |
possibly damaging |
Het |
Rspo2 |
A |
C |
15: 42,885,933 (GRCm39) |
V241G |
probably benign |
Het |
Smg1 |
T |
A |
7: 117,759,469 (GRCm39) |
|
probably benign |
Het |
Snph |
T |
C |
2: 151,435,722 (GRCm39) |
D402G |
probably damaging |
Het |
Spta1 |
A |
G |
1: 174,041,632 (GRCm39) |
D1334G |
probably benign |
Het |
Stard13 |
C |
A |
5: 151,016,294 (GRCm39) |
|
probably null |
Het |
Sufu |
A |
G |
19: 46,413,541 (GRCm39) |
M141V |
probably damaging |
Het |
Sytl2 |
T |
A |
7: 90,057,635 (GRCm39) |
V831D |
possibly damaging |
Het |
Tc2n |
T |
C |
12: 101,617,414 (GRCm39) |
E335G |
possibly damaging |
Het |
Tex11 |
C |
A |
X: 99,977,021 (GRCm39) |
A487S |
possibly damaging |
Het |
Tmcc1 |
T |
A |
6: 116,020,441 (GRCm39) |
H118L |
probably damaging |
Het |
Tulp4 |
C |
T |
17: 6,282,055 (GRCm39) |
H695Y |
probably damaging |
Het |
Vmn1r209 |
A |
C |
13: 22,989,785 (GRCm39) |
L302V |
probably null |
Het |
Vmn2r117 |
C |
T |
17: 23,679,080 (GRCm39) |
V715I |
probably benign |
Het |
Vopp1 |
A |
T |
6: 57,766,964 (GRCm39) |
Y37* |
probably null |
Het |
Xrn1 |
A |
G |
9: 95,863,973 (GRCm39) |
T528A |
probably benign |
Het |
Zfhx2 |
T |
C |
14: 55,302,662 (GRCm39) |
D1774G |
probably benign |
Het |
Zfp955b |
T |
A |
17: 33,521,129 (GRCm39) |
D199E |
probably benign |
Het |
Zp2 |
T |
C |
7: 119,734,475 (GRCm39) |
S525G |
probably benign |
Het |
|
Other mutations in Cyp2e1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00706:Cyp2e1
|
APN |
7 |
140,349,066 (GRCm39) |
missense |
probably benign |
0.17 |
IGL01755:Cyp2e1
|
APN |
7 |
140,354,469 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01884:Cyp2e1
|
APN |
7 |
140,353,663 (GRCm39) |
missense |
probably benign |
0.16 |
IGL01950:Cyp2e1
|
APN |
7 |
140,344,874 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01964:Cyp2e1
|
APN |
7 |
140,343,779 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02430:Cyp2e1
|
APN |
7 |
140,350,139 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02505:Cyp2e1
|
APN |
7 |
140,349,069 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02596:Cyp2e1
|
APN |
7 |
140,350,031 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02725:Cyp2e1
|
APN |
7 |
140,343,828 (GRCm39) |
missense |
probably null |
1.00 |
IGL02887:Cyp2e1
|
APN |
7 |
140,343,824 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03114:Cyp2e1
|
APN |
7 |
140,353,042 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03146:Cyp2e1
|
APN |
7 |
140,350,134 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03340:Cyp2e1
|
APN |
7 |
140,344,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R1396:Cyp2e1
|
UTSW |
7 |
140,352,992 (GRCm39) |
missense |
probably damaging |
0.98 |
R2111:Cyp2e1
|
UTSW |
7 |
140,353,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R2230:Cyp2e1
|
UTSW |
7 |
140,344,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R2231:Cyp2e1
|
UTSW |
7 |
140,344,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R2383:Cyp2e1
|
UTSW |
7 |
140,349,981 (GRCm39) |
missense |
probably benign |
0.06 |
R3778:Cyp2e1
|
UTSW |
7 |
140,343,822 (GRCm39) |
missense |
possibly damaging |
0.58 |
R4707:Cyp2e1
|
UTSW |
7 |
140,343,821 (GRCm39) |
missense |
possibly damaging |
0.58 |
R4751:Cyp2e1
|
UTSW |
7 |
140,354,629 (GRCm39) |
nonsense |
probably null |
|
R4784:Cyp2e1
|
UTSW |
7 |
140,343,821 (GRCm39) |
missense |
possibly damaging |
0.58 |
R4792:Cyp2e1
|
UTSW |
7 |
140,353,588 (GRCm39) |
missense |
probably benign |
|
R4917:Cyp2e1
|
UTSW |
7 |
140,354,527 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4934:Cyp2e1
|
UTSW |
7 |
140,350,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R5092:Cyp2e1
|
UTSW |
7 |
140,354,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R5388:Cyp2e1
|
UTSW |
7 |
140,343,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R5423:Cyp2e1
|
UTSW |
7 |
140,350,031 (GRCm39) |
missense |
probably benign |
0.01 |
R6740:Cyp2e1
|
UTSW |
7 |
140,343,693 (GRCm39) |
unclassified |
probably benign |
|
R7065:Cyp2e1
|
UTSW |
7 |
140,343,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R7154:Cyp2e1
|
UTSW |
7 |
140,350,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R8054:Cyp2e1
|
UTSW |
7 |
140,350,871 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9130:Cyp2e1
|
UTSW |
7 |
140,353,022 (GRCm39) |
missense |
probably damaging |
0.99 |
|