Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700029F12Rik |
T |
C |
13: 97,166,738 (GRCm39) |
T93A |
unknown |
Het |
Adgrg6 |
T |
A |
10: 14,302,515 (GRCm39) |
H938L |
probably benign |
Het |
Aff1 |
A |
G |
5: 103,997,365 (GRCm39) |
Y1153C |
probably damaging |
Het |
Akr1c20 |
T |
A |
13: 4,564,388 (GRCm39) |
I42L |
probably benign |
Het |
Atad2b |
T |
A |
12: 5,082,064 (GRCm39) |
N1324K |
probably benign |
Het |
Aurka |
T |
A |
2: 172,201,760 (GRCm39) |
I270F |
probably damaging |
Het |
Camk2g |
A |
T |
14: 20,815,498 (GRCm39) |
D189E |
probably damaging |
Het |
Cc2d2b |
A |
G |
19: 40,804,299 (GRCm39) |
D942G |
unknown |
Het |
Ccnd1 |
A |
C |
7: 144,491,770 (GRCm39) |
S90A |
probably benign |
Het |
Cfap77 |
G |
T |
2: 28,852,741 (GRCm39) |
T177K |
probably damaging |
Het |
Chd9 |
A |
G |
8: 91,721,220 (GRCm39) |
N1003D |
unknown |
Het |
Chga |
C |
G |
12: 102,525,613 (GRCm39) |
Q85E |
possibly damaging |
Het |
Cnot1 |
T |
C |
8: 96,496,209 (GRCm39) |
S322G |
probably benign |
Het |
Cyp8b1 |
C |
A |
9: 121,744,294 (GRCm39) |
S346I |
probably benign |
Het |
Cysltr2 |
T |
A |
14: 73,266,906 (GRCm39) |
H268L |
probably damaging |
Het |
Dnah11 |
T |
C |
12: 117,884,704 (GRCm39) |
T3783A |
probably benign |
Het |
Dock3 |
C |
T |
9: 106,959,713 (GRCm39) |
V109I |
probably benign |
Het |
Dscc1 |
A |
G |
15: 54,953,674 (GRCm39) |
C50R |
probably benign |
Het |
Dtx3l |
T |
A |
16: 35,753,277 (GRCm39) |
D443V |
probably damaging |
Het |
Ephb6 |
A |
G |
6: 41,592,911 (GRCm39) |
H383R |
probably benign |
Het |
Fdft1 |
A |
G |
14: 63,400,869 (GRCm39) |
I88T |
probably damaging |
Het |
Fmo3 |
C |
A |
1: 162,794,524 (GRCm39) |
W182L |
probably benign |
Het |
Folh1 |
T |
A |
7: 86,406,158 (GRCm39) |
Q305L |
probably benign |
Het |
Gale |
C |
T |
4: 135,692,975 (GRCm39) |
Q73* |
probably null |
Het |
Gm9195 |
T |
C |
14: 72,699,885 (GRCm39) |
M1154V |
unknown |
Het |
Grip1 |
G |
A |
10: 119,874,569 (GRCm39) |
E778K |
possibly damaging |
Het |
Gtsf1l |
T |
C |
2: 162,929,052 (GRCm39) |
T144A |
probably benign |
Het |
Itpkc |
T |
C |
7: 26,927,222 (GRCm39) |
T231A |
probably benign |
Het |
Kng2 |
C |
A |
16: 22,822,737 (GRCm39) |
C205F |
probably damaging |
Het |
Ldlrap1 |
T |
G |
4: 134,476,661 (GRCm39) |
N244T |
probably benign |
Het |
Lingo2 |
A |
G |
4: 35,709,750 (GRCm39) |
F77L |
possibly damaging |
Het |
Lrit2 |
A |
G |
14: 36,790,936 (GRCm39) |
D205G |
probably damaging |
Het |
Lrrc34 |
T |
C |
3: 30,697,467 (GRCm39) |
D88G |
probably damaging |
Het |
Macf1 |
T |
C |
4: 123,366,136 (GRCm39) |
E2875G |
probably benign |
Het |
Med13 |
G |
T |
11: 86,177,345 (GRCm39) |
Q1584K |
possibly damaging |
Het |
Naip5 |
C |
G |
13: 100,367,269 (GRCm39) |
A276P |
probably damaging |
Het |
Ndufv2 |
A |
G |
17: 66,394,503 (GRCm39) |
Y121H |
probably damaging |
Het |
Or4f52 |
T |
A |
2: 111,061,521 (GRCm39) |
I206F |
probably damaging |
Het |
Peg12 |
T |
C |
7: 62,113,297 (GRCm39) |
T267A |
unknown |
Het |
Pkig |
A |
G |
2: 163,567,375 (GRCm39) |
|
probably null |
Het |
Prkch |
C |
G |
12: 73,747,078 (GRCm39) |
T319S |
probably benign |
Het |
Rhobtb1 |
T |
C |
10: 69,115,202 (GRCm39) |
S534P |
probably damaging |
Het |
Riok2 |
A |
G |
17: 17,607,814 (GRCm39) |
N454S |
probably benign |
Het |
Ryr2 |
T |
A |
13: 11,701,935 (GRCm39) |
K2907N |
possibly damaging |
Het |
Sdc3 |
C |
T |
4: 130,546,048 (GRCm39) |
P136S |
unknown |
Het |
Slc37a3 |
G |
A |
6: 39,322,844 (GRCm39) |
L371F |
probably damaging |
Het |
Slc3a1 |
A |
T |
17: 85,371,419 (GRCm39) |
H657L |
probably damaging |
Het |
Slc7a13 |
T |
A |
4: 19,819,033 (GRCm39) |
Y78N |
probably benign |
Het |
Slfn8 |
G |
T |
11: 82,907,838 (GRCm39) |
A235E |
probably damaging |
Het |
Snap91 |
T |
A |
9: 86,707,094 (GRCm39) |
D232V |
possibly damaging |
Het |
Stap2 |
C |
A |
17: 56,309,914 (GRCm39) |
S79I |
probably damaging |
Het |
Stra6l |
T |
C |
4: 45,884,602 (GRCm39) |
V544A |
probably damaging |
Het |
Syn2 |
T |
C |
6: 115,251,219 (GRCm39) |
|
probably null |
Het |
Tctn1 |
G |
A |
5: 122,388,527 (GRCm39) |
P284S |
possibly damaging |
Het |
Terb2 |
G |
A |
2: 122,018,475 (GRCm39) |
M77I |
probably benign |
Het |
Trim80 |
G |
T |
11: 115,338,757 (GRCm39) |
R529L |
possibly damaging |
Het |
Washc2 |
T |
C |
6: 116,186,048 (GRCm39) |
L86P |
possibly damaging |
Het |
Zfp74 |
A |
T |
7: 29,631,845 (GRCm39) |
F133Y |
probably benign |
Het |
Zfp987 |
T |
A |
4: 146,060,752 (GRCm39) |
N61K |
probably benign |
Het |
|
Other mutations in Lpcat2b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00566:Lpcat2b
|
APN |
5 |
107,581,670 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01620:Lpcat2b
|
APN |
5 |
107,581,759 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02268:Lpcat2b
|
APN |
5 |
107,581,982 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03103:Lpcat2b
|
APN |
5 |
107,581,414 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4431001:Lpcat2b
|
UTSW |
5 |
107,581,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R0967:Lpcat2b
|
UTSW |
5 |
107,582,084 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1259:Lpcat2b
|
UTSW |
5 |
107,581,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R1508:Lpcat2b
|
UTSW |
5 |
107,581,330 (GRCm39) |
missense |
probably damaging |
0.99 |
R1976:Lpcat2b
|
UTSW |
5 |
107,581,716 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2352:Lpcat2b
|
UTSW |
5 |
107,581,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R4617:Lpcat2b
|
UTSW |
5 |
107,581,865 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5187:Lpcat2b
|
UTSW |
5 |
107,582,001 (GRCm39) |
nonsense |
probably null |
|
R5696:Lpcat2b
|
UTSW |
5 |
107,580,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R6170:Lpcat2b
|
UTSW |
5 |
107,581,760 (GRCm39) |
missense |
probably benign |
0.10 |
R6199:Lpcat2b
|
UTSW |
5 |
107,581,171 (GRCm39) |
missense |
probably benign |
0.03 |
R7316:Lpcat2b
|
UTSW |
5 |
107,580,979 (GRCm39) |
missense |
not run |
|
R8850:Lpcat2b
|
UTSW |
5 |
107,580,692 (GRCm39) |
missense |
probably benign |
|
R8928:Lpcat2b
|
UTSW |
5 |
107,580,913 (GRCm39) |
missense |
probably benign |
|
Z1088:Lpcat2b
|
UTSW |
5 |
107,581,177 (GRCm39) |
missense |
probably damaging |
1.00 |
|