Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsl4 |
G |
T |
X: 141,126,184 (GRCm39) |
D313E |
probably damaging |
Het |
Aifm3 |
A |
C |
16: 17,321,405 (GRCm39) |
K453T |
probably benign |
Het |
Anks1b |
T |
C |
10: 90,733,100 (GRCm39) |
|
probably benign |
Het |
Arfgef1 |
T |
C |
1: 10,229,840 (GRCm39) |
D1287G |
probably damaging |
Het |
Bcl3 |
G |
A |
7: 19,546,416 (GRCm39) |
Q140* |
probably null |
Het |
Bnipl |
T |
G |
3: 95,150,045 (GRCm39) |
R316S |
probably damaging |
Het |
Cacna1i |
T |
A |
15: 80,275,958 (GRCm39) |
H1916Q |
probably benign |
Het |
Ccdc171 |
C |
T |
4: 83,599,432 (GRCm39) |
A749V |
probably damaging |
Het |
Cul7 |
G |
T |
17: 46,969,641 (GRCm39) |
M969I |
possibly damaging |
Het |
Cylc2 |
A |
G |
4: 51,228,360 (GRCm39) |
T144A |
probably benign |
Het |
Cyp2c50 |
A |
T |
19: 40,086,495 (GRCm39) |
H294L |
probably damaging |
Het |
D430041D05Rik |
T |
C |
2: 104,085,306 (GRCm39) |
K1081R |
probably damaging |
Het |
D930020B18Rik |
A |
G |
10: 121,519,866 (GRCm39) |
K456R |
probably benign |
Het |
Drd2 |
A |
G |
9: 49,313,389 (GRCm39) |
N186S |
possibly damaging |
Het |
Fanci |
A |
T |
7: 79,098,925 (GRCm39) |
E1306D |
probably benign |
Het |
Fbxl21 |
T |
A |
13: 56,675,522 (GRCm39) |
|
probably benign |
Het |
Galk2 |
T |
A |
2: 125,729,807 (GRCm39) |
Y63N |
probably damaging |
Het |
Git2 |
T |
C |
5: 114,905,166 (GRCm39) |
D97G |
probably damaging |
Het |
Gm8258 |
T |
A |
5: 104,923,940 (GRCm39) |
|
noncoding transcript |
Het |
Irf4 |
G |
T |
13: 30,941,454 (GRCm39) |
S270I |
probably damaging |
Het |
Itgb3 |
C |
A |
11: 104,524,216 (GRCm39) |
|
probably benign |
Het |
Itpr2 |
A |
C |
6: 146,081,727 (GRCm39) |
I2299R |
probably damaging |
Het |
Lig4 |
T |
C |
8: 10,023,673 (GRCm39) |
I36V |
probably benign |
Het |
Nedd9 |
A |
G |
13: 41,492,111 (GRCm39) |
V133A |
probably damaging |
Het |
Nup133 |
A |
C |
8: 124,665,869 (GRCm39) |
Y185* |
probably null |
Het |
Or51b6b |
A |
T |
7: 103,310,194 (GRCm39) |
F88I |
probably benign |
Het |
Or5d14 |
T |
C |
2: 87,880,128 (GRCm39) |
Y280C |
possibly damaging |
Het |
Or6c3 |
A |
G |
10: 129,309,080 (GRCm39) |
H173R |
probably damaging |
Het |
Pgbd5 |
T |
A |
8: 125,101,138 (GRCm39) |
T373S |
possibly damaging |
Het |
Ppp1r8 |
T |
C |
4: 132,555,480 (GRCm39) |
E246G |
probably benign |
Het |
Rmnd5b |
C |
T |
11: 51,518,727 (GRCm39) |
V89M |
probably damaging |
Het |
Rnf123 |
T |
C |
9: 107,935,555 (GRCm39) |
I969V |
probably damaging |
Het |
Ror2 |
A |
G |
13: 53,265,124 (GRCm39) |
I656T |
probably damaging |
Het |
Sgsm1 |
T |
C |
5: 113,411,356 (GRCm39) |
E503G |
probably benign |
Het |
Smgc |
T |
A |
15: 91,744,882 (GRCm39) |
S381T |
possibly damaging |
Het |
Tlr4 |
T |
G |
4: 66,759,504 (GRCm39) |
F766V |
possibly damaging |
Het |
Tnc |
T |
C |
4: 63,918,938 (GRCm39) |
T1162A |
probably damaging |
Het |
Usp39 |
A |
G |
6: 72,315,476 (GRCm39) |
V156A |
probably damaging |
Het |
Zdhhc5 |
A |
G |
2: 84,521,538 (GRCm39) |
Y352H |
probably damaging |
Het |
Zfp646 |
A |
G |
7: 127,478,137 (GRCm39) |
T105A |
probably benign |
Het |
|
Other mutations in Ceacam18 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00426:Ceacam18
|
APN |
7 |
43,288,780 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00585:Ceacam18
|
APN |
7 |
43,286,435 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0001:Ceacam18
|
UTSW |
7 |
43,286,300 (GRCm39) |
missense |
possibly damaging |
0.58 |
R0227:Ceacam18
|
UTSW |
7 |
43,288,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R1524:Ceacam18
|
UTSW |
7 |
43,288,779 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1647:Ceacam18
|
UTSW |
7 |
43,288,689 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1768:Ceacam18
|
UTSW |
7 |
43,297,918 (GRCm39) |
missense |
probably benign |
0.00 |
R1828:Ceacam18
|
UTSW |
7 |
43,288,880 (GRCm39) |
missense |
probably benign |
0.19 |
R3751:Ceacam18
|
UTSW |
7 |
43,291,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R4870:Ceacam18
|
UTSW |
7 |
43,291,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R5259:Ceacam18
|
UTSW |
7 |
43,286,536 (GRCm39) |
critical splice donor site |
probably null |
|
R5358:Ceacam18
|
UTSW |
7 |
43,286,497 (GRCm39) |
missense |
possibly damaging |
0.57 |
R5368:Ceacam18
|
UTSW |
7 |
43,291,458 (GRCm39) |
missense |
probably benign |
0.08 |
R5810:Ceacam18
|
UTSW |
7 |
43,286,382 (GRCm39) |
missense |
probably benign |
0.00 |
R5817:Ceacam18
|
UTSW |
7 |
43,291,265 (GRCm39) |
missense |
probably benign |
0.07 |
R5835:Ceacam18
|
UTSW |
7 |
43,286,382 (GRCm39) |
missense |
probably benign |
0.00 |
R7113:Ceacam18
|
UTSW |
7 |
43,291,400 (GRCm39) |
missense |
probably benign |
|
R7138:Ceacam18
|
UTSW |
7 |
43,288,706 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7275:Ceacam18
|
UTSW |
7 |
43,291,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R7502:Ceacam18
|
UTSW |
7 |
43,286,298 (GRCm39) |
missense |
probably damaging |
0.99 |
R8849:Ceacam18
|
UTSW |
7 |
43,294,967 (GRCm39) |
missense |
probably benign |
0.00 |
R9119:Ceacam18
|
UTSW |
7 |
43,288,909 (GRCm39) |
missense |
probably benign |
|
R9347:Ceacam18
|
UTSW |
7 |
43,294,915 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9663:Ceacam18
|
UTSW |
7 |
43,288,764 (GRCm39) |
missense |
probably damaging |
1.00 |
|