Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930523C07Rik |
T |
C |
1: 159,902,826 (GRCm39) |
L32P |
probably damaging |
Het |
4930563M21Rik |
T |
C |
9: 55,916,564 (GRCm39) |
T38A |
unknown |
Het |
Abcb6 |
T |
C |
1: 75,151,002 (GRCm39) |
N563D |
probably damaging |
Het |
Ak4 |
T |
C |
4: 101,317,850 (GRCm39) |
F140S |
probably damaging |
Het |
Arhgap27 |
T |
A |
11: 103,229,519 (GRCm39) |
R296S |
probably damaging |
Het |
Atxn7l1 |
A |
C |
12: 33,376,001 (GRCm39) |
K98N |
probably damaging |
Het |
Bex6 |
G |
T |
16: 32,005,224 (GRCm39) |
D11Y |
probably damaging |
Het |
Camta1 |
T |
C |
4: 151,228,489 (GRCm39) |
D781G |
probably damaging |
Het |
Capn7 |
A |
G |
14: 31,092,936 (GRCm39) |
D800G |
probably benign |
Het |
Carmil2 |
G |
A |
8: 106,419,008 (GRCm39) |
V716I |
probably benign |
Het |
Cdk5 |
C |
A |
5: 24,625,782 (GRCm39) |
D144Y |
probably damaging |
Het |
Cep85 |
T |
C |
4: 133,880,925 (GRCm39) |
|
probably benign |
Het |
Chd5 |
T |
A |
4: 152,450,829 (GRCm39) |
L651Q |
probably damaging |
Het |
Cimap1d |
T |
A |
10: 79,475,835 (GRCm39) |
H243L |
probably damaging |
Het |
Clcn7 |
C |
T |
17: 25,368,233 (GRCm39) |
Q261* |
probably null |
Het |
Cntnap2 |
T |
A |
6: 46,324,079 (GRCm39) |
F576Y |
probably damaging |
Het |
Col11a1 |
G |
A |
3: 113,925,263 (GRCm39) |
G815D |
unknown |
Het |
Col4a4 |
T |
A |
1: 82,501,591 (GRCm39) |
R387S |
unknown |
Het |
Cse1l |
T |
A |
2: 166,781,845 (GRCm39) |
V663D |
probably damaging |
Het |
Csf2rb2 |
G |
T |
15: 78,169,206 (GRCm39) |
Q650K |
probably damaging |
Het |
Ctnnd2 |
A |
G |
15: 30,847,497 (GRCm39) |
D696G |
possibly damaging |
Het |
Dnah7c |
T |
A |
1: 46,728,112 (GRCm39) |
C2937S |
possibly damaging |
Het |
Epha10 |
A |
T |
4: 124,796,476 (GRCm39) |
Q395L |
|
Het |
Fam167a |
T |
A |
14: 63,689,769 (GRCm39) |
V22E |
probably benign |
Het |
Fan1 |
T |
A |
7: 64,022,234 (GRCm39) |
N340Y |
probably damaging |
Het |
Gabra4 |
A |
G |
5: 71,781,295 (GRCm39) |
I372T |
probably benign |
Het |
Gpt |
A |
G |
15: 76,580,972 (GRCm39) |
|
probably benign |
Het |
H2-K2 |
C |
T |
17: 34,215,833 (GRCm39) |
G336D |
possibly damaging |
Het |
Hapstr1 |
C |
T |
16: 8,648,232 (GRCm39) |
|
probably benign |
Het |
Hoxd8 |
T |
C |
2: 74,535,070 (GRCm39) |
|
probably null |
Het |
Ilrun |
C |
T |
17: 27,986,863 (GRCm39) |
A288T |
unknown |
Het |
Kdm5d |
T |
G |
Y: 927,355 (GRCm39) |
D658E |
possibly damaging |
Het |
Krt25 |
G |
A |
11: 99,208,169 (GRCm39) |
T353M |
probably benign |
Het |
Lonp2 |
T |
C |
8: 87,440,717 (GRCm39) |
L778P |
probably damaging |
Het |
Mak |
T |
A |
13: 41,202,813 (GRCm39) |
I212F |
probably damaging |
Het |
Mastl |
T |
A |
2: 23,023,566 (GRCm39) |
R386W |
possibly damaging |
Het |
Mis18bp1 |
A |
G |
12: 65,195,673 (GRCm39) |
I697T |
possibly damaging |
Het |
Nek5 |
G |
A |
8: 22,578,922 (GRCm39) |
T415I |
probably benign |
Het |
Neu3 |
T |
A |
7: 99,463,435 (GRCm39) |
N96I |
probably benign |
Het |
Nxph2 |
T |
C |
2: 23,290,107 (GRCm39) |
V153A |
possibly damaging |
Het |
Or10a3 |
A |
T |
7: 108,480,571 (GRCm39) |
F81I |
probably damaging |
Het |
Or5b102 |
G |
A |
19: 13,040,638 (GRCm39) |
|
probably benign |
Het |
Or8b4 |
A |
G |
9: 37,830,460 (GRCm39) |
D169G |
probably benign |
Het |
Otogl |
T |
C |
10: 107,644,476 (GRCm39) |
T1257A |
probably benign |
Het |
Pcdh10 |
G |
A |
3: 45,333,694 (GRCm39) |
V3M |
probably benign |
Het |
Pitpnm1 |
G |
A |
19: 4,162,145 (GRCm39) |
R1017Q |
probably null |
Het |
Plcb3 |
A |
C |
19: 6,932,463 (GRCm39) |
H1065Q |
probably benign |
Het |
Plcb3 |
A |
T |
19: 6,936,267 (GRCm39) |
M752K |
probably damaging |
Het |
Plch1 |
T |
C |
3: 63,605,557 (GRCm39) |
E1449G |
probably benign |
Het |
Plekha4 |
T |
A |
7: 45,198,695 (GRCm39) |
C573S |
probably benign |
Het |
Plin2 |
T |
C |
4: 86,575,638 (GRCm39) |
I304V |
possibly damaging |
Het |
Pnp2 |
G |
A |
14: 51,201,838 (GRCm39) |
V275I |
probably benign |
Het |
Polr1a |
G |
A |
6: 71,908,644 (GRCm39) |
A490T |
possibly damaging |
Het |
Ppp1r12b |
A |
G |
1: 134,883,354 (GRCm39) |
F56S |
probably damaging |
Het |
Ptk2 |
GA |
G |
15: 73,170,048 (GRCm39) |
|
probably null |
Het |
Rb1cc1 |
C |
A |
1: 6,315,443 (GRCm39) |
R473S |
probably damaging |
Het |
Rcc2 |
G |
A |
4: 140,429,586 (GRCm39) |
C40Y |
probably benign |
Het |
Rdx |
T |
C |
9: 51,976,946 (GRCm39) |
V65A |
probably damaging |
Het |
Rpl27rt |
T |
C |
18: 34,870,582 (GRCm39) |
F39L |
probably damaging |
Het |
Rps6ka5 |
A |
G |
12: 100,540,055 (GRCm39) |
|
probably null |
Het |
Samd5 |
C |
T |
10: 9,550,641 (GRCm39) |
V23M |
probably damaging |
Het |
Scn9a |
T |
G |
2: 66,345,774 (GRCm39) |
R1117S |
probably benign |
Het |
Scrn1 |
T |
A |
6: 54,497,758 (GRCm39) |
I278L |
probably benign |
Het |
Sec31b |
G |
T |
19: 44,507,804 (GRCm39) |
P747T |
probably damaging |
Het |
Sipa1l2 |
A |
T |
8: 126,195,269 (GRCm39) |
V823E |
probably damaging |
Het |
Slc2a13 |
T |
C |
15: 91,400,619 (GRCm39) |
N201S |
probably damaging |
Het |
Slc30a3 |
C |
A |
5: 31,247,395 (GRCm39) |
|
probably benign |
Het |
Snx31 |
C |
A |
15: 36,523,606 (GRCm39) |
V359F |
probably damaging |
Het |
Sstr2 |
A |
G |
11: 113,515,099 (GRCm39) |
E6G |
probably benign |
Het |
Stc2 |
C |
A |
11: 31,317,806 (GRCm39) |
E72* |
probably null |
Het |
Tead1 |
C |
T |
7: 112,358,721 (GRCm39) |
P11L |
probably benign |
Het |
Tmem51 |
T |
C |
4: 141,759,059 (GRCm39) |
T230A |
probably damaging |
Het |
Tmem63c |
A |
T |
12: 87,118,972 (GRCm39) |
K301* |
probably null |
Het |
Tns3 |
G |
C |
11: 8,442,773 (GRCm39) |
A530G |
probably benign |
Het |
Trat1 |
T |
C |
16: 48,562,600 (GRCm39) |
D70G |
probably damaging |
Het |
Trex1 |
T |
A |
9: 108,887,397 (GRCm39) |
E198V |
probably damaging |
Het |
Ttn |
T |
G |
2: 76,570,072 (GRCm39) |
R26940S |
probably damaging |
Het |
Uba2 |
T |
C |
7: 33,867,835 (GRCm39) |
K34R |
possibly damaging |
Het |
Vps13d |
A |
C |
4: 144,701,753 (GRCm39) |
M4376R |
|
Het |
Zfp157 |
C |
A |
5: 138,454,336 (GRCm39) |
T178K |
probably damaging |
Het |
Zfp318 |
T |
A |
17: 46,710,692 (GRCm39) |
V805D |
possibly damaging |
Het |
|
Other mutations in Lrrc66 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00507:Lrrc66
|
APN |
5 |
73,764,457 (GRCm39) |
missense |
probably benign |
0.10 |
IGL00913:Lrrc66
|
APN |
5 |
73,765,499 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL00954:Lrrc66
|
APN |
5 |
73,765,741 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01061:Lrrc66
|
APN |
5 |
73,772,842 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01343:Lrrc66
|
APN |
5 |
73,765,806 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01714:Lrrc66
|
APN |
5 |
73,787,320 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01822:Lrrc66
|
APN |
5 |
73,787,311 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02005:Lrrc66
|
APN |
5 |
73,766,077 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02166:Lrrc66
|
APN |
5 |
73,764,634 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02380:Lrrc66
|
APN |
5 |
73,787,009 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL03162:Lrrc66
|
APN |
5 |
73,764,725 (GRCm39) |
missense |
probably benign |
|
BB002:Lrrc66
|
UTSW |
5 |
73,765,835 (GRCm39) |
missense |
possibly damaging |
0.81 |
BB012:Lrrc66
|
UTSW |
5 |
73,765,835 (GRCm39) |
missense |
possibly damaging |
0.81 |
D4043:Lrrc66
|
UTSW |
5 |
73,764,869 (GRCm39) |
missense |
probably benign |
0.03 |
R0126:Lrrc66
|
UTSW |
5 |
73,764,431 (GRCm39) |
missense |
probably benign |
0.10 |
R0437:Lrrc66
|
UTSW |
5 |
73,765,030 (GRCm39) |
missense |
probably benign |
0.23 |
R0638:Lrrc66
|
UTSW |
5 |
73,772,816 (GRCm39) |
splice site |
probably benign |
|
R0658:Lrrc66
|
UTSW |
5 |
73,768,287 (GRCm39) |
missense |
probably benign |
0.40 |
R0729:Lrrc66
|
UTSW |
5 |
73,765,757 (GRCm39) |
missense |
probably benign |
|
R1603:Lrrc66
|
UTSW |
5 |
73,764,769 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1774:Lrrc66
|
UTSW |
5 |
73,768,198 (GRCm39) |
missense |
probably benign |
0.16 |
R1831:Lrrc66
|
UTSW |
5 |
73,764,769 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1832:Lrrc66
|
UTSW |
5 |
73,764,769 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1902:Lrrc66
|
UTSW |
5 |
73,764,965 (GRCm39) |
missense |
probably damaging |
0.99 |
R2858:Lrrc66
|
UTSW |
5 |
73,764,646 (GRCm39) |
missense |
probably benign |
0.08 |
R4097:Lrrc66
|
UTSW |
5 |
73,765,047 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4164:Lrrc66
|
UTSW |
5 |
73,787,119 (GRCm39) |
splice site |
probably null |
|
R4582:Lrrc66
|
UTSW |
5 |
73,765,580 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4708:Lrrc66
|
UTSW |
5 |
73,787,005 (GRCm39) |
missense |
probably benign |
0.06 |
R4856:Lrrc66
|
UTSW |
5 |
73,765,910 (GRCm39) |
missense |
probably benign |
0.10 |
R4886:Lrrc66
|
UTSW |
5 |
73,765,910 (GRCm39) |
missense |
probably benign |
0.10 |
R5074:Lrrc66
|
UTSW |
5 |
73,765,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R5464:Lrrc66
|
UTSW |
5 |
73,765,622 (GRCm39) |
missense |
probably benign |
0.05 |
R5640:Lrrc66
|
UTSW |
5 |
73,765,977 (GRCm39) |
missense |
probably benign |
0.00 |
R5709:Lrrc66
|
UTSW |
5 |
73,766,206 (GRCm39) |
missense |
probably benign |
|
R5811:Lrrc66
|
UTSW |
5 |
73,772,860 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6146:Lrrc66
|
UTSW |
5 |
73,765,432 (GRCm39) |
missense |
probably benign |
0.10 |
R7037:Lrrc66
|
UTSW |
5 |
73,764,504 (GRCm39) |
missense |
probably benign |
0.10 |
R7041:Lrrc66
|
UTSW |
5 |
73,765,899 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7141:Lrrc66
|
UTSW |
5 |
73,787,320 (GRCm39) |
missense |
probably benign |
0.10 |
R7201:Lrrc66
|
UTSW |
5 |
73,787,240 (GRCm39) |
missense |
probably benign |
0.11 |
R7250:Lrrc66
|
UTSW |
5 |
73,768,224 (GRCm39) |
missense |
probably benign |
0.03 |
R7367:Lrrc66
|
UTSW |
5 |
73,765,724 (GRCm39) |
missense |
probably benign |
0.13 |
R7773:Lrrc66
|
UTSW |
5 |
73,764,664 (GRCm39) |
missense |
probably damaging |
0.98 |
R7925:Lrrc66
|
UTSW |
5 |
73,765,835 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8167:Lrrc66
|
UTSW |
5 |
73,786,952 (GRCm39) |
nonsense |
probably null |
|
R8552:Lrrc66
|
UTSW |
5 |
73,768,228 (GRCm39) |
missense |
probably benign |
0.16 |
R8834:Lrrc66
|
UTSW |
5 |
73,765,928 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8992:Lrrc66
|
UTSW |
5 |
73,787,227 (GRCm39) |
missense |
probably benign |
0.04 |
R9017:Lrrc66
|
UTSW |
5 |
73,765,244 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9051:Lrrc66
|
UTSW |
5 |
73,765,268 (GRCm39) |
missense |
probably benign |
0.00 |
R9051:Lrrc66
|
UTSW |
5 |
73,765,267 (GRCm39) |
missense |
probably benign |
0.05 |
|