Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700018F24Rik |
A |
G |
5: 144,980,192 (GRCm39) |
D47G |
probably damaging |
Het |
4930550C14Rik |
A |
T |
9: 53,334,258 (GRCm39) |
K167M |
possibly damaging |
Het |
Abhd16b |
A |
G |
2: 181,135,806 (GRCm39) |
N236S |
probably benign |
Het |
Ahnak |
T |
G |
19: 8,990,101 (GRCm39) |
V3795G |
probably damaging |
Het |
Atg2b |
A |
T |
12: 105,602,725 (GRCm39) |
M1606K |
probably damaging |
Het |
Bmt2 |
A |
T |
6: 13,630,611 (GRCm39) |
I187K |
probably damaging |
Het |
Cep250 |
C |
T |
2: 155,812,042 (GRCm39) |
A446V |
unknown |
Het |
Cep290 |
A |
G |
10: 100,349,782 (GRCm39) |
N610D |
possibly damaging |
Het |
Ctps1 |
C |
T |
4: 120,406,743 (GRCm39) |
D338N |
probably benign |
Het |
Ctsz |
A |
T |
2: 174,275,421 (GRCm39) |
I118N |
probably benign |
Het |
Depdc1b |
A |
G |
13: 108,525,094 (GRCm39) |
E483G |
probably null |
Het |
Dhh |
T |
C |
15: 98,795,976 (GRCm39) |
S60G |
probably damaging |
Het |
Dpagt1 |
T |
C |
9: 44,237,446 (GRCm39) |
|
probably benign |
Het |
Dpy19l1 |
T |
C |
9: 24,359,102 (GRCm39) |
K162R |
probably damaging |
Het |
Dynap |
T |
C |
18: 70,375,093 (GRCm39) |
T41A |
possibly damaging |
Het |
Dyrk4 |
T |
C |
6: 126,871,783 (GRCm39) |
N162D |
probably benign |
Het |
Efcab3 |
A |
G |
11: 104,954,415 (GRCm39) |
K5090E |
probably benign |
Het |
Eml5 |
T |
A |
12: 98,776,829 (GRCm39) |
T1429S |
probably damaging |
Het |
Fbn2 |
C |
T |
18: 58,286,928 (GRCm39) |
G244R |
probably damaging |
Het |
Fer1l5 |
A |
G |
1: 36,456,897 (GRCm39) |
D1625G |
probably benign |
Het |
Frmd4b |
G |
A |
6: 97,283,477 (GRCm39) |
T484M |
possibly damaging |
Het |
Hhat |
T |
C |
1: 192,431,250 (GRCm39) |
E33G |
probably damaging |
Het |
Ifngr1 |
A |
G |
10: 19,485,360 (GRCm39) |
D453G |
probably damaging |
Het |
Itpr3 |
T |
A |
17: 27,335,628 (GRCm39) |
I2246N |
possibly damaging |
Het |
Larp4b |
T |
G |
13: 9,195,537 (GRCm39) |
I212S |
probably damaging |
Het |
Map1lc3a |
A |
G |
2: 155,118,926 (GRCm39) |
K30R |
possibly damaging |
Het |
Mapk8ip1 |
A |
G |
2: 92,215,166 (GRCm39) |
Y652H |
probably damaging |
Het |
Med23 |
A |
G |
10: 24,780,334 (GRCm39) |
E994G |
probably benign |
Het |
Mep1b |
A |
T |
18: 21,208,714 (GRCm39) |
D30V |
probably benign |
Het |
Mki67 |
C |
A |
7: 135,297,364 (GRCm39) |
A2557S |
possibly damaging |
Het |
Mki67 |
T |
C |
7: 135,300,129 (GRCm39) |
D1635G |
probably benign |
Het |
Msantd5f6 |
A |
G |
4: 73,320,167 (GRCm39) |
L204P |
probably damaging |
Het |
Mup3 |
A |
T |
4: 62,003,472 (GRCm39) |
D132E |
probably benign |
Het |
Myo15b |
A |
T |
11: 115,781,780 (GRCm39) |
T2830S |
unknown |
Het |
Myocd |
T |
A |
11: 65,069,287 (GRCm39) |
H979L |
probably damaging |
Het |
Nvl |
A |
T |
1: 180,958,001 (GRCm39) |
N260K |
probably benign |
Het |
Or2a57 |
T |
A |
6: 43,213,056 (GRCm39) |
H171Q |
probably benign |
Het |
Or2d2b |
T |
A |
7: 106,705,664 (GRCm39) |
T135S |
probably benign |
Het |
Or4d2 |
T |
A |
11: 87,784,645 (GRCm39) |
Y35F |
probably damaging |
Het |
Pdha2 |
C |
A |
3: 140,917,649 (GRCm39) |
|
probably benign |
Het |
Peg10 |
GC |
GCTCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
Phtf2 |
A |
C |
5: 20,969,249 (GRCm39) |
V687G |
probably damaging |
Het |
Plagl2 |
C |
T |
2: 153,074,346 (GRCm39) |
G185D |
possibly damaging |
Het |
Ppp1r3e |
A |
G |
14: 55,113,946 (GRCm39) |
V242A |
probably benign |
Het |
Proser3 |
A |
G |
7: 30,239,458 (GRCm39) |
S549P |
possibly damaging |
Het |
Prrc2c |
A |
G |
1: 162,533,630 (GRCm39) |
V995A |
unknown |
Het |
Ptpn13 |
A |
G |
5: 103,649,266 (GRCm39) |
H223R |
probably benign |
Het |
Rsf1 |
CG |
CGTCGGCGGGG |
7: 97,229,115 (GRCm39) |
|
probably benign |
Het |
Scn11a |
T |
C |
9: 119,587,565 (GRCm39) |
E1393G |
probably damaging |
Het |
Sipa1l1 |
T |
A |
12: 82,479,612 (GRCm39) |
S1432T |
possibly damaging |
Het |
Slc10a5 |
G |
C |
3: 10,399,670 (GRCm39) |
A330G |
probably benign |
Het |
Slc2a5 |
A |
C |
4: 150,224,270 (GRCm39) |
N293H |
probably damaging |
Het |
Spmap1 |
A |
T |
11: 97,663,572 (GRCm39) |
Y93N |
probably damaging |
Het |
Spmip4 |
C |
T |
6: 50,561,391 (GRCm39) |
R176H |
probably damaging |
Het |
Sptbn1 |
T |
C |
11: 30,073,869 (GRCm39) |
E1400G |
possibly damaging |
Het |
Stk33 |
T |
A |
7: 108,935,280 (GRCm39) |
I171F |
probably damaging |
Het |
Syne1 |
G |
A |
10: 5,161,945 (GRCm39) |
H5450Y |
probably benign |
Het |
Tbcd |
G |
C |
11: 121,387,679 (GRCm39) |
|
probably benign |
Het |
Tkt |
T |
A |
14: 30,288,884 (GRCm39) |
|
probably benign |
Het |
Tpra1 |
A |
T |
6: 88,888,726 (GRCm39) |
M303L |
probably benign |
Het |
Ubr3 |
T |
C |
2: 69,752,651 (GRCm39) |
S303P |
probably damaging |
Het |
Uqcrc1 |
T |
C |
9: 108,776,721 (GRCm39) |
F341S |
probably damaging |
Het |
Vmn1r223 |
T |
C |
13: 23,434,248 (GRCm39) |
S281P |
possibly damaging |
Het |
Vmn1r32 |
C |
A |
6: 66,530,189 (GRCm39) |
A196S |
probably benign |
Het |
Zfp644 |
G |
T |
5: 106,785,467 (GRCm39) |
T360N |
probably benign |
Het |
|
Other mutations in Lilra5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02189:Lilra5
|
APN |
7 |
4,240,968 (GRCm39) |
missense |
probably benign |
|
IGL02281:Lilra5
|
APN |
7 |
4,241,782 (GRCm39) |
missense |
probably benign |
0.00 |
R0458:Lilra5
|
UTSW |
7 |
4,241,218 (GRCm39) |
missense |
probably benign |
0.26 |
R0611:Lilra5
|
UTSW |
7 |
4,245,232 (GRCm39) |
missense |
probably benign |
|
R0685:Lilra5
|
UTSW |
7 |
4,244,956 (GRCm39) |
splice site |
probably benign |
|
R3195:Lilra5
|
UTSW |
7 |
4,241,756 (GRCm39) |
missense |
probably damaging |
0.96 |
R4726:Lilra5
|
UTSW |
7 |
4,240,957 (GRCm39) |
missense |
probably benign |
0.00 |
R4745:Lilra5
|
UTSW |
7 |
4,245,076 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4836:Lilra5
|
UTSW |
7 |
4,241,713 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6034:Lilra5
|
UTSW |
7 |
4,245,133 (GRCm39) |
missense |
probably benign |
0.33 |
R6034:Lilra5
|
UTSW |
7 |
4,245,133 (GRCm39) |
missense |
probably benign |
0.33 |
R6263:Lilra5
|
UTSW |
7 |
4,241,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R6266:Lilra5
|
UTSW |
7 |
4,244,927 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6285:Lilra5
|
UTSW |
7 |
4,245,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R6292:Lilra5
|
UTSW |
7 |
4,241,338 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6344:Lilra5
|
UTSW |
7 |
4,241,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R6861:Lilra5
|
UTSW |
7 |
4,244,931 (GRCm39) |
missense |
probably benign |
0.14 |
R8353:Lilra5
|
UTSW |
7 |
4,240,971 (GRCm39) |
missense |
probably benign |
0.06 |
R8681:Lilra5
|
UTSW |
7 |
4,241,216 (GRCm39) |
missense |
probably benign |
0.17 |
R8844:Lilra5
|
UTSW |
7 |
4,241,663 (GRCm39) |
missense |
probably damaging |
0.99 |
R8867:Lilra5
|
UTSW |
7 |
4,241,165 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9393:Lilra5
|
UTSW |
7 |
4,240,758 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R9646:Lilra5
|
UTSW |
7 |
4,244,907 (GRCm39) |
missense |
probably damaging |
0.98 |
|