Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930407I10Rik |
A |
G |
15: 81,949,810 (GRCm39) |
K1236E |
probably damaging |
Het |
Actl7a |
A |
T |
4: 56,744,353 (GRCm39) |
E293D |
possibly damaging |
Het |
Adamts2 |
T |
C |
11: 50,667,082 (GRCm39) |
Y460H |
probably damaging |
Het |
Aoc1 |
G |
A |
6: 48,883,044 (GRCm39) |
V307I |
probably benign |
Het |
Ar |
C |
T |
X: 97,358,492 (GRCm39) |
H756Y |
probably damaging |
Het |
Atg3 |
C |
T |
16: 45,004,048 (GRCm39) |
R224W |
probably benign |
Het |
Atp5po |
G |
A |
16: 91,483,201 (GRCm39) |
P47S |
probably damaging |
Het |
Bicd1 |
A |
G |
6: 149,311,054 (GRCm39) |
E43G |
probably damaging |
Het |
Ccdc88c |
A |
G |
12: 100,934,059 (GRCm39) |
|
probably benign |
Het |
Cd36 |
T |
A |
5: 18,002,126 (GRCm39) |
R292* |
probably null |
Het |
Cdc45 |
C |
T |
16: 18,617,479 (GRCm39) |
M200I |
probably benign |
Het |
Cdh23 |
T |
C |
10: 60,227,580 (GRCm39) |
D1167G |
probably damaging |
Het |
Cdk5rap1 |
A |
G |
2: 154,207,880 (GRCm39) |
|
probably null |
Het |
Chd6 |
A |
G |
2: 160,881,270 (GRCm39) |
|
probably benign |
Het |
Chd7 |
A |
T |
4: 8,826,519 (GRCm39) |
Y961F |
probably damaging |
Het |
Cpe |
T |
C |
8: 65,145,829 (GRCm39) |
E52G |
probably benign |
Het |
Cpne5 |
C |
T |
17: 29,379,311 (GRCm39) |
G491S |
probably damaging |
Het |
Csmd3 |
A |
T |
15: 47,567,503 (GRCm39) |
|
probably benign |
Het |
Ctbp2 |
T |
A |
7: 132,600,940 (GRCm39) |
T608S |
probably benign |
Het |
Cybb |
A |
G |
X: 9,335,439 (GRCm39) |
|
probably null |
Het |
Daam2 |
T |
C |
17: 49,797,282 (GRCm39) |
T168A |
possibly damaging |
Het |
Dnah5 |
G |
T |
15: 28,307,422 (GRCm39) |
V1717F |
possibly damaging |
Het |
Dse |
G |
A |
10: 34,029,158 (GRCm39) |
T644I |
probably damaging |
Het |
Dtd2 |
A |
C |
12: 52,051,708 (GRCm39) |
Y45* |
probably null |
Het |
Fgfr1op2 |
T |
A |
6: 146,491,509 (GRCm39) |
M124K |
probably benign |
Het |
Flii |
T |
C |
11: 60,610,685 (GRCm39) |
D537G |
probably benign |
Het |
Fntb |
T |
A |
12: 76,944,145 (GRCm39) |
I217N |
probably benign |
Het |
Foxi1 |
A |
G |
11: 34,155,860 (GRCm39) |
S257P |
probably benign |
Het |
Fyn |
G |
A |
10: 39,402,798 (GRCm39) |
R190H |
probably damaging |
Het |
Gm28557 |
T |
A |
13: 67,223,008 (GRCm39) |
T8S |
probably benign |
Het |
Gramd1b |
T |
C |
9: 40,209,306 (GRCm39) |
K873E |
probably damaging |
Het |
Grb10 |
T |
C |
11: 11,895,503 (GRCm39) |
T329A |
probably benign |
Het |
Haus5 |
A |
G |
7: 30,356,675 (GRCm39) |
L477P |
probably damaging |
Het |
Hectd4 |
A |
T |
5: 121,491,944 (GRCm39) |
E3761V |
possibly damaging |
Het |
Ift172 |
T |
C |
5: 31,421,840 (GRCm39) |
I930V |
probably benign |
Het |
Itprid1 |
T |
A |
6: 55,945,631 (GRCm39) |
V784D |
probably benign |
Het |
Izumo2 |
A |
G |
7: 44,358,560 (GRCm39) |
|
probably benign |
Het |
Map4k4 |
A |
G |
1: 40,053,257 (GRCm39) |
|
probably benign |
Het |
Morc1 |
A |
G |
16: 48,436,123 (GRCm39) |
S753G |
probably damaging |
Het |
Mpzl2 |
C |
T |
9: 44,955,590 (GRCm39) |
T167I |
probably damaging |
Het |
Mta2 |
T |
A |
19: 8,926,532 (GRCm39) |
I491N |
probably damaging |
Het |
Myo18b |
A |
T |
5: 113,025,951 (GRCm39) |
I33N |
unknown |
Het |
Nub1 |
C |
T |
5: 24,908,462 (GRCm39) |
H404Y |
possibly damaging |
Het |
Or10ak13 |
T |
C |
4: 118,639,531 (GRCm39) |
M84V |
probably damaging |
Het |
Or4f58 |
A |
T |
2: 111,851,458 (GRCm39) |
V247E |
probably damaging |
Het |
Or5d47 |
T |
C |
2: 87,804,068 (GRCm39) |
N314D |
probably benign |
Het |
Or8d2b |
T |
C |
9: 38,788,784 (GRCm39) |
L104S |
probably benign |
Het |
Ralyl |
A |
T |
3: 13,842,094 (GRCm39) |
M77L |
probably benign |
Het |
Rap1gap |
T |
A |
4: 137,454,364 (GRCm39) |
V649E |
probably benign |
Het |
Rnf40 |
C |
A |
7: 127,195,744 (GRCm39) |
Q663K |
probably damaging |
Het |
Slc22a18 |
T |
C |
7: 143,052,837 (GRCm39) |
L354P |
probably damaging |
Het |
Slc9a8 |
T |
C |
2: 167,309,597 (GRCm39) |
|
probably benign |
Het |
Surf4 |
C |
T |
2: 26,815,619 (GRCm39) |
|
probably null |
Het |
T |
A |
T |
17: 8,654,069 (GRCm39) |
N85Y |
probably damaging |
Het |
Tanc1 |
A |
G |
2: 59,630,216 (GRCm39) |
E732G |
probably damaging |
Het |
Tas2r138 |
A |
G |
6: 40,589,649 (GRCm39) |
V199A |
possibly damaging |
Het |
Trim43b |
T |
C |
9: 88,967,541 (GRCm39) |
Y365C |
possibly damaging |
Het |
Ubd |
T |
C |
17: 37,506,573 (GRCm39) |
L153P |
probably damaging |
Het |
Xpnpep2 |
A |
C |
X: 47,215,786 (GRCm39) |
M513L |
probably benign |
Het |
Zar1l |
C |
T |
5: 150,441,210 (GRCm39) |
G139R |
probably damaging |
Het |
Zc3hav1 |
T |
G |
6: 38,309,926 (GRCm39) |
T299P |
probably damaging |
Het |
Zfp236 |
C |
A |
18: 82,676,120 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Cd33 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00948:Cd33
|
APN |
7 |
43,178,982 (GRCm39) |
intron |
probably benign |
|
IGL01025:Cd33
|
APN |
7 |
43,182,329 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01593:Cd33
|
APN |
7 |
43,179,705 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02080:Cd33
|
APN |
7 |
43,178,274 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02519:Cd33
|
APN |
7 |
43,178,153 (GRCm39) |
utr 3 prime |
probably benign |
|
1mM(1):Cd33
|
UTSW |
7 |
43,178,217 (GRCm39) |
utr 3 prime |
probably benign |
|
R0751:Cd33
|
UTSW |
7 |
43,181,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R1513:Cd33
|
UTSW |
7 |
43,181,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R1542:Cd33
|
UTSW |
7 |
43,181,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R1752:Cd33
|
UTSW |
7 |
43,181,722 (GRCm39) |
missense |
probably benign |
0.24 |
R1928:Cd33
|
UTSW |
7 |
43,179,303 (GRCm39) |
missense |
probably benign |
0.41 |
R2045:Cd33
|
UTSW |
7 |
43,179,316 (GRCm39) |
missense |
probably benign |
0.00 |
R2127:Cd33
|
UTSW |
7 |
43,179,699 (GRCm39) |
missense |
possibly damaging |
0.72 |
R3433:Cd33
|
UTSW |
7 |
43,179,331 (GRCm39) |
missense |
probably benign |
0.00 |
R4760:Cd33
|
UTSW |
7 |
43,178,919 (GRCm39) |
missense |
probably benign |
|
R4810:Cd33
|
UTSW |
7 |
43,182,134 (GRCm39) |
missense |
probably damaging |
0.99 |
R5387:Cd33
|
UTSW |
7 |
43,181,477 (GRCm39) |
nonsense |
probably null |
|
R5611:Cd33
|
UTSW |
7 |
43,181,542 (GRCm39) |
missense |
probably damaging |
0.97 |
R5796:Cd33
|
UTSW |
7 |
43,182,480 (GRCm39) |
critical splice donor site |
probably null |
|
R8021:Cd33
|
UTSW |
7 |
43,178,262 (GRCm39) |
missense |
unknown |
|
R8193:Cd33
|
UTSW |
7 |
43,181,696 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8993:Cd33
|
UTSW |
7 |
43,182,871 (GRCm39) |
unclassified |
probably benign |
|
R9495:Cd33
|
UTSW |
7 |
43,182,150 (GRCm39) |
missense |
probably benign |
0.09 |
R9514:Cd33
|
UTSW |
7 |
43,182,150 (GRCm39) |
missense |
probably benign |
0.09 |
R9590:Cd33
|
UTSW |
7 |
43,179,637 (GRCm39) |
missense |
probably benign |
0.00 |
|