Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgb |
A |
T |
10: 10,216,254 (GRCm39) |
S1485T |
probably benign |
Het |
Akap9 |
A |
G |
5: 4,120,351 (GRCm39) |
Y3589C |
probably damaging |
Het |
Alkbh8 |
T |
C |
9: 3,385,153 (GRCm39) |
Y482H |
probably damaging |
Het |
Appl1 |
G |
A |
14: 26,649,801 (GRCm39) |
T575M |
probably damaging |
Het |
Arhgap21 |
T |
C |
2: 20,855,102 (GRCm39) |
E1420G |
probably damaging |
Het |
Asic3 |
A |
T |
5: 24,621,997 (GRCm39) |
Y419F |
probably benign |
Het |
Atg7 |
A |
G |
6: 114,672,624 (GRCm39) |
Y279C |
probably damaging |
Het |
Braf |
G |
A |
6: 39,600,610 (GRCm39) |
P616L |
probably damaging |
Het |
Btnl2 |
T |
C |
17: 34,577,109 (GRCm39) |
M88T |
possibly damaging |
Het |
Cacna1s |
T |
C |
1: 135,996,780 (GRCm39) |
F127S |
possibly damaging |
Het |
Cd47 |
A |
G |
16: 49,688,205 (GRCm39) |
I42V |
probably benign |
Het |
Cox8b |
T |
A |
7: 140,478,918 (GRCm39) |
K66* |
probably null |
Het |
Diras2 |
T |
A |
13: 52,662,059 (GRCm39) |
I83F |
probably damaging |
Het |
Dlg2 |
T |
A |
7: 91,361,008 (GRCm39) |
|
probably null |
Het |
Dnah8 |
G |
A |
17: 31,073,872 (GRCm39) |
R4514H |
probably damaging |
Het |
Dnai1 |
G |
A |
4: 41,602,615 (GRCm39) |
R113H |
probably damaging |
Het |
Dolpp1 |
T |
C |
2: 30,287,500 (GRCm39) |
L204P |
probably damaging |
Het |
Fam170a |
C |
T |
18: 50,415,271 (GRCm39) |
P306S |
probably benign |
Het |
Fbxl12 |
A |
T |
9: 20,550,268 (GRCm39) |
|
probably null |
Het |
Fndc3a |
T |
A |
14: 72,777,648 (GRCm39) |
I1186F |
probably benign |
Het |
Gm12886 |
T |
A |
4: 121,274,667 (GRCm39) |
D71V |
probably damaging |
Het |
H3c8 |
T |
C |
13: 23,719,722 (GRCm39) |
V36A |
possibly damaging |
Het |
Ica1 |
A |
G |
6: 8,659,021 (GRCm39) |
|
probably benign |
Het |
Ighv8-11 |
A |
G |
12: 115,530,771 (GRCm39) |
I119T |
possibly damaging |
Het |
Ism1 |
A |
T |
2: 139,573,931 (GRCm39) |
R94* |
probably null |
Het |
Kbtbd11 |
T |
A |
8: 15,079,118 (GRCm39) |
C572* |
probably null |
Het |
Kcnk15 |
T |
C |
2: 163,700,214 (GRCm39) |
L132P |
probably damaging |
Het |
Lrmda |
T |
A |
14: 22,077,399 (GRCm39) |
|
probably benign |
Het |
Mei1 |
A |
G |
15: 81,987,405 (GRCm39) |
H399R |
possibly damaging |
Het |
Mrtfb |
C |
T |
16: 13,203,557 (GRCm39) |
A201V |
probably damaging |
Het |
Ncstn |
G |
A |
1: 171,895,462 (GRCm39) |
T562M |
possibly damaging |
Het |
Nudt4 |
A |
T |
10: 95,385,367 (GRCm39) |
|
probably null |
Het |
Omp |
T |
C |
7: 97,794,420 (GRCm39) |
N69S |
probably benign |
Het |
Or10d3 |
A |
C |
9: 39,461,418 (GRCm39) |
C250G |
probably damaging |
Het |
Or4a75 |
A |
T |
2: 89,448,503 (GRCm39) |
I11N |
possibly damaging |
Het |
Pak1 |
C |
T |
7: 97,503,704 (GRCm39) |
P13L |
probably damaging |
Het |
Pde4d |
T |
A |
13: 110,087,866 (GRCm39) |
C744* |
probably null |
Het |
Pelp1 |
T |
C |
11: 70,289,026 (GRCm39) |
Y240C |
possibly damaging |
Het |
Pou2f1 |
G |
C |
1: 165,722,538 (GRCm39) |
P349R |
probably damaging |
Het |
Ptprk |
A |
G |
10: 28,259,619 (GRCm39) |
D353G |
probably damaging |
Het |
Ptprs |
A |
G |
17: 56,724,485 (GRCm39) |
F1152S |
probably damaging |
Het |
Rnf135 |
G |
T |
11: 80,087,743 (GRCm39) |
A231S |
probably benign |
Het |
Rpn1 |
G |
A |
6: 88,067,282 (GRCm39) |
|
probably null |
Het |
Rreb1 |
T |
A |
13: 38,131,074 (GRCm39) |
D1409E |
probably benign |
Het |
Sipa1l2 |
G |
A |
8: 126,200,323 (GRCm39) |
H668Y |
probably damaging |
Het |
Slc35a5 |
A |
T |
16: 44,967,685 (GRCm39) |
I138N |
probably damaging |
Het |
Slc35d1 |
T |
C |
4: 103,065,321 (GRCm39) |
K187E |
possibly damaging |
Het |
Slc44a2 |
A |
T |
9: 21,254,273 (GRCm39) |
I212F |
possibly damaging |
Het |
Slc7a1 |
G |
A |
5: 148,272,343 (GRCm39) |
R445* |
probably null |
Het |
Snapc4 |
A |
G |
2: 26,255,440 (GRCm39) |
L1028P |
probably benign |
Het |
Snrnp40 |
C |
T |
4: 130,262,068 (GRCm39) |
T152I |
possibly damaging |
Het |
Spata31f1a |
T |
C |
4: 42,851,472 (GRCm39) |
E228G |
probably benign |
Het |
Spink4 |
T |
A |
4: 40,929,136 (GRCm39) |
C54S |
probably damaging |
Het |
Tex2 |
C |
T |
11: 106,437,566 (GRCm39) |
W203* |
probably null |
Het |
Tmcc1 |
T |
C |
6: 116,110,783 (GRCm39) |
E170G |
possibly damaging |
Het |
Ttc23l |
CT |
CTTGGATT |
15: 10,537,648 (GRCm39) |
|
probably benign |
Het |
Ttc23l |
G |
A |
15: 10,537,652 (GRCm39) |
S206L |
probably benign |
Het |
Ttll6 |
A |
G |
11: 96,024,747 (GRCm39) |
N46D |
probably benign |
Het |
Txk |
T |
A |
5: 72,865,078 (GRCm39) |
K266* |
probably null |
Het |
Uggt2 |
T |
C |
14: 119,278,930 (GRCm39) |
E859G |
probably damaging |
Het |
Uros |
A |
T |
7: 133,304,120 (GRCm39) |
M1K |
probably null |
Het |
Vps13b |
T |
A |
15: 35,671,528 (GRCm39) |
I1677N |
probably damaging |
Het |
Zbtb5 |
A |
G |
4: 44,994,863 (GRCm39) |
|
probably null |
Het |
Zfp760 |
A |
G |
17: 21,941,143 (GRCm39) |
Y106C |
probably damaging |
Het |
|
Other mutations in C1rb |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R4806:C1rb
|
UTSW |
6 |
124,551,908 (GRCm39) |
missense |
probably benign |
0.18 |
R5095:C1rb
|
UTSW |
6 |
124,557,272 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5572:C1rb
|
UTSW |
6 |
124,557,758 (GRCm39) |
missense |
probably benign |
|
R6223:C1rb
|
UTSW |
6 |
124,551,539 (GRCm39) |
missense |
probably benign |
0.06 |
R6769:C1rb
|
UTSW |
6 |
124,554,364 (GRCm39) |
missense |
probably benign |
0.00 |
R6771:C1rb
|
UTSW |
6 |
124,554,364 (GRCm39) |
missense |
probably benign |
0.00 |
R7204:C1rb
|
UTSW |
6 |
124,554,386 (GRCm39) |
missense |
probably benign |
|
R7335:C1rb
|
UTSW |
6 |
124,552,238 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7341:C1rb
|
UTSW |
6 |
124,554,411 (GRCm39) |
nonsense |
probably null |
|
R7554:C1rb
|
UTSW |
6 |
124,557,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R7604:C1rb
|
UTSW |
6 |
124,557,443 (GRCm39) |
missense |
not run |
|
R7753:C1rb
|
UTSW |
6 |
124,557,390 (GRCm39) |
missense |
probably benign |
0.00 |
R7813:C1rb
|
UTSW |
6 |
124,557,488 (GRCm39) |
missense |
probably benign |
0.00 |
R8423:C1rb
|
UTSW |
6 |
124,551,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R8549:C1rb
|
UTSW |
6 |
124,551,498 (GRCm39) |
missense |
probably benign |
0.04 |
R8835:C1rb
|
UTSW |
6 |
124,552,217 (GRCm39) |
missense |
probably benign |
0.02 |
R9056:C1rb
|
UTSW |
6 |
124,553,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R9091:C1rb
|
UTSW |
6 |
124,551,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R9270:C1rb
|
UTSW |
6 |
124,551,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R9289:C1rb
|
UTSW |
6 |
124,552,272 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9390:C1rb
|
UTSW |
6 |
124,557,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R9460:C1rb
|
UTSW |
6 |
124,557,865 (GRCm39) |
missense |
probably benign |
0.00 |
|