Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700109H08Rik |
A |
G |
5: 3,632,150 (GRCm39) |
D160G |
probably damaging |
Het |
Aak1 |
A |
G |
6: 86,936,152 (GRCm39) |
|
probably benign |
Het |
Anp32e |
A |
G |
3: 95,845,224 (GRCm39) |
|
probably benign |
Het |
Aspscr1 |
T |
A |
11: 120,568,405 (GRCm39) |
L61Q |
probably damaging |
Het |
Btrc |
A |
G |
19: 45,491,589 (GRCm39) |
I89M |
probably damaging |
Het |
Ccdc175 |
G |
A |
12: 72,221,899 (GRCm39) |
T141M |
probably damaging |
Het |
Cep70 |
G |
A |
9: 99,157,775 (GRCm39) |
V225I |
probably damaging |
Het |
Cilk1 |
A |
G |
9: 78,047,301 (GRCm39) |
E67G |
probably damaging |
Het |
Col4a1 |
T |
C |
8: 11,281,950 (GRCm39) |
|
probably benign |
Het |
Cpne1 |
T |
C |
2: 155,920,137 (GRCm39) |
Y214C |
probably damaging |
Het |
Crtc3 |
T |
C |
7: 80,268,406 (GRCm39) |
|
probably null |
Het |
Cul2 |
C |
T |
18: 3,434,052 (GRCm39) |
A683V |
probably damaging |
Het |
Ddx47 |
A |
G |
6: 134,994,114 (GRCm39) |
N131D |
probably benign |
Het |
Dnah7b |
T |
G |
1: 46,138,768 (GRCm39) |
|
probably benign |
Het |
Dnai2 |
T |
C |
11: 114,642,737 (GRCm39) |
L446P |
probably damaging |
Het |
Ergic2 |
T |
C |
6: 148,106,317 (GRCm39) |
T58A |
possibly damaging |
Het |
Erlin2 |
A |
G |
8: 27,519,703 (GRCm39) |
|
probably benign |
Het |
Fermt2 |
T |
C |
14: 45,742,113 (GRCm39) |
T78A |
probably damaging |
Het |
Flg2 |
G |
T |
3: 93,127,438 (GRCm39) |
G97* |
probably null |
Het |
Gm7356 |
A |
G |
17: 14,221,537 (GRCm39) |
I164T |
probably damaging |
Het |
Gucy1a2 |
T |
A |
9: 3,894,719 (GRCm39) |
|
probably benign |
Het |
Heatr5b |
C |
T |
17: 79,122,969 (GRCm39) |
R670H |
probably damaging |
Het |
Hspa4l |
T |
C |
3: 40,727,090 (GRCm39) |
V476A |
possibly damaging |
Het |
Itpkc |
A |
T |
7: 26,927,475 (GRCm39) |
D146E |
possibly damaging |
Het |
Kcnk3 |
T |
C |
5: 30,779,324 (GRCm39) |
F125L |
probably damaging |
Het |
Kif12 |
T |
A |
4: 63,086,033 (GRCm39) |
M411L |
probably benign |
Het |
Krtap24-1 |
T |
C |
16: 88,409,094 (GRCm39) |
S11G |
probably benign |
Het |
Lilra6 |
A |
T |
7: 3,915,991 (GRCm39) |
H289Q |
possibly damaging |
Het |
Musk |
A |
C |
4: 58,356,496 (GRCm39) |
N469H |
probably benign |
Het |
Myom1 |
A |
G |
17: 71,413,349 (GRCm39) |
|
probably benign |
Het |
Nagpa |
A |
G |
16: 5,019,357 (GRCm39) |
V46A |
possibly damaging |
Het |
Or4k37 |
T |
A |
2: 111,159,590 (GRCm39) |
Y275* |
probably null |
Het |
Or5h25 |
T |
A |
16: 58,930,536 (GRCm39) |
T146S |
probably benign |
Het |
Or8g17 |
T |
C |
9: 38,930,312 (GRCm39) |
N175S |
probably benign |
Het |
Parp6 |
T |
A |
9: 59,538,021 (GRCm39) |
V222E |
probably benign |
Het |
Pde3b |
T |
A |
7: 114,105,483 (GRCm39) |
S472T |
probably damaging |
Het |
Peak1 |
A |
G |
9: 56,134,490 (GRCm39) |
S1314P |
probably damaging |
Het |
Pgc |
A |
G |
17: 48,039,792 (GRCm39) |
Y62C |
probably damaging |
Het |
Pitpnm2 |
A |
G |
5: 124,278,665 (GRCm39) |
C189R |
probably damaging |
Het |
Pla2g15 |
G |
T |
8: 106,886,828 (GRCm39) |
Q106H |
probably benign |
Het |
Pla2g4c |
T |
A |
7: 13,064,019 (GRCm39) |
S93T |
probably damaging |
Het |
Retsat |
A |
G |
6: 72,580,642 (GRCm39) |
T207A |
possibly damaging |
Het |
Slc25a32 |
A |
G |
15: 38,963,300 (GRCm39) |
Y174H |
probably benign |
Het |
Slc35f2 |
T |
A |
9: 53,717,026 (GRCm39) |
|
probably benign |
Het |
Snx19 |
A |
G |
9: 30,343,556 (GRCm39) |
N572S |
possibly damaging |
Het |
Sos2 |
A |
G |
12: 69,663,958 (GRCm39) |
Y476H |
probably benign |
Het |
Ssh2 |
A |
T |
11: 77,316,413 (GRCm39) |
N296I |
probably damaging |
Het |
Sspo |
G |
T |
6: 48,459,601 (GRCm39) |
R3320L |
probably benign |
Het |
Synj2 |
A |
G |
17: 6,047,192 (GRCm39) |
I166V |
probably benign |
Het |
Tpp2 |
T |
C |
1: 43,979,391 (GRCm39) |
V96A |
probably benign |
Het |
Vmn2r3 |
A |
T |
3: 64,183,031 (GRCm39) |
W223R |
probably damaging |
Het |
Wdr17 |
T |
C |
8: 55,146,089 (GRCm39) |
|
probably null |
Het |
Zfr2 |
T |
A |
10: 81,080,546 (GRCm39) |
C407S |
probably damaging |
Het |
|
Other mutations in Rbks |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02019:Rbks
|
APN |
5 |
31,817,361 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02618:Rbks
|
APN |
5 |
31,781,863 (GRCm39) |
nonsense |
probably null |
|
IGL02678:Rbks
|
APN |
5 |
31,830,757 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02947:Rbks
|
APN |
5 |
31,817,407 (GRCm39) |
missense |
probably benign |
|
R0334:Rbks
|
UTSW |
5 |
31,781,863 (GRCm39) |
nonsense |
probably null |
|
R1441:Rbks
|
UTSW |
5 |
31,817,341 (GRCm39) |
missense |
probably benign |
|
R2568:Rbks
|
UTSW |
5 |
31,823,096 (GRCm39) |
missense |
probably damaging |
0.99 |
R4545:Rbks
|
UTSW |
5 |
31,781,912 (GRCm39) |
missense |
probably benign |
0.10 |
R4546:Rbks
|
UTSW |
5 |
31,781,912 (GRCm39) |
missense |
probably benign |
0.10 |
R4591:Rbks
|
UTSW |
5 |
31,817,352 (GRCm39) |
missense |
possibly damaging |
0.52 |
R4833:Rbks
|
UTSW |
5 |
31,781,859 (GRCm39) |
missense |
probably benign |
0.00 |
R4967:Rbks
|
UTSW |
5 |
31,781,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R5076:Rbks
|
UTSW |
5 |
31,807,795 (GRCm39) |
nonsense |
probably null |
|
R5214:Rbks
|
UTSW |
5 |
31,807,736 (GRCm39) |
intron |
probably benign |
|
R6051:Rbks
|
UTSW |
5 |
31,809,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R6194:Rbks
|
UTSW |
5 |
31,824,234 (GRCm39) |
missense |
probably benign |
0.05 |
R6607:Rbks
|
UTSW |
5 |
31,805,136 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7246:Rbks
|
UTSW |
5 |
31,805,127 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8270:Rbks
|
UTSW |
5 |
31,807,810 (GRCm39) |
intron |
probably benign |
|
R9070:Rbks
|
UTSW |
5 |
31,854,890 (GRCm39) |
missense |
probably benign |
0.02 |
Z1177:Rbks
|
UTSW |
5 |
31,805,207 (GRCm39) |
missense |
probably damaging |
0.98 |
|