Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsl5 |
C |
T |
19: 55,261,265 (GRCm39) |
A74V |
probably benign |
Het |
Adh4 |
C |
T |
3: 138,134,788 (GRCm39) |
|
probably benign |
Het |
Aldh1a3 |
G |
A |
7: 66,058,978 (GRCm39) |
T239I |
probably damaging |
Het |
Anxa9 |
A |
G |
3: 95,207,847 (GRCm39) |
|
probably null |
Het |
Atp5me |
C |
A |
5: 108,581,899 (GRCm39) |
K28N |
probably damaging |
Het |
C9 |
T |
G |
15: 6,489,149 (GRCm39) |
Y169D |
probably benign |
Het |
Chat |
T |
A |
14: 32,168,849 (GRCm39) |
|
probably null |
Het |
Csmd3 |
C |
T |
15: 47,874,479 (GRCm39) |
E706K |
probably benign |
Het |
Ctbs |
A |
G |
3: 146,160,867 (GRCm39) |
K145E |
probably benign |
Het |
Dennd5a |
A |
G |
7: 109,533,302 (GRCm39) |
M156T |
probably damaging |
Het |
Dhx29 |
A |
G |
13: 113,101,756 (GRCm39) |
Y1275C |
probably damaging |
Het |
Dpp10 |
A |
T |
1: 123,295,596 (GRCm39) |
F517Y |
probably benign |
Het |
Dst |
G |
A |
1: 34,227,990 (GRCm39) |
W1536* |
probably null |
Het |
Galc |
T |
C |
12: 98,218,340 (GRCm39) |
T171A |
possibly damaging |
Het |
Gsap |
T |
C |
5: 21,431,246 (GRCm39) |
I190T |
probably damaging |
Het |
Hars2 |
A |
T |
18: 36,922,630 (GRCm39) |
R388* |
probably null |
Het |
Itgbl1 |
T |
A |
14: 124,065,211 (GRCm39) |
S122T |
possibly damaging |
Het |
Jhy |
G |
T |
9: 40,872,260 (GRCm39) |
T83K |
possibly damaging |
Het |
Kcne4 |
A |
T |
1: 78,795,525 (GRCm39) |
M58L |
possibly damaging |
Het |
Lamc3 |
T |
A |
2: 31,802,119 (GRCm39) |
I509N |
probably damaging |
Het |
Lpar6 |
T |
C |
14: 73,476,506 (GRCm39) |
S156P |
probably damaging |
Het |
Man2c1 |
T |
C |
9: 57,048,840 (GRCm39) |
|
probably benign |
Het |
Marchf11 |
T |
C |
15: 26,409,285 (GRCm39) |
I328T |
possibly damaging |
Het |
Mc3r |
T |
A |
2: 172,091,290 (GRCm39) |
C171S |
probably benign |
Het |
Muc4 |
A |
T |
16: 32,577,001 (GRCm39) |
Q2167L |
unknown |
Het |
Myom1 |
T |
C |
17: 71,406,988 (GRCm39) |
V1135A |
possibly damaging |
Het |
Nectin1 |
C |
T |
9: 43,702,555 (GRCm39) |
R101* |
probably null |
Het |
Nxpe4 |
T |
C |
9: 48,305,440 (GRCm39) |
S277P |
possibly damaging |
Het |
Or1e35 |
T |
C |
11: 73,798,303 (GRCm39) |
N5S |
probably damaging |
Het |
Or2a52 |
T |
A |
6: 43,144,637 (GRCm39) |
V215E |
probably damaging |
Het |
Or52r1c |
G |
A |
7: 102,735,582 (GRCm39) |
V281I |
probably benign |
Het |
Or5b106 |
T |
A |
19: 13,123,614 (GRCm39) |
K136N |
probably benign |
Het |
Or5w19 |
A |
C |
2: 87,698,488 (GRCm39) |
D51A |
probably damaging |
Het |
Pappa2 |
G |
T |
1: 158,684,948 (GRCm39) |
N730K |
probably damaging |
Het |
Prepl |
A |
G |
17: 85,373,709 (GRCm39) |
V586A |
probably damaging |
Het |
Prrc2a |
T |
C |
17: 35,368,529 (GRCm39) |
Y2098C |
probably damaging |
Het |
Rdh16 |
G |
A |
10: 127,637,176 (GRCm39) |
C37Y |
probably damaging |
Het |
Rnd1 |
A |
T |
15: 98,571,746 (GRCm39) |
M100K |
probably benign |
Het |
Sema3c |
A |
G |
5: 17,877,504 (GRCm39) |
N204D |
probably damaging |
Het |
Susd4 |
A |
G |
1: 182,686,026 (GRCm39) |
|
probably null |
Het |
Taar7f |
G |
T |
10: 23,926,239 (GRCm39) |
A278S |
possibly damaging |
Het |
Tle4 |
T |
A |
19: 14,522,178 (GRCm39) |
M122L |
probably benign |
Het |
Trim9 |
C |
T |
12: 70,295,125 (GRCm39) |
V662I |
probably benign |
Het |
Vmn2r10 |
C |
A |
5: 109,150,345 (GRCm39) |
C233F |
probably damaging |
Het |
Vmn2r98 |
A |
C |
17: 19,285,521 (GRCm39) |
T114P |
possibly damaging |
Het |
Zfyve21 |
C |
T |
12: 111,794,247 (GRCm39) |
|
probably benign |
Het |
Zng1 |
T |
C |
19: 24,918,140 (GRCm39) |
E210G |
possibly damaging |
Het |
|
Other mutations in Igsf21 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01538:Igsf21
|
APN |
4 |
139,755,029 (GRCm39) |
splice site |
probably benign |
|
IGL01613:Igsf21
|
APN |
4 |
139,834,675 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1458:Igsf21
|
UTSW |
4 |
139,755,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R1464:Igsf21
|
UTSW |
4 |
139,761,836 (GRCm39) |
missense |
probably benign |
|
R1464:Igsf21
|
UTSW |
4 |
139,761,836 (GRCm39) |
missense |
probably benign |
|
R1793:Igsf21
|
UTSW |
4 |
139,761,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R1913:Igsf21
|
UTSW |
4 |
139,834,623 (GRCm39) |
missense |
probably benign |
|
R2220:Igsf21
|
UTSW |
4 |
139,755,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R4013:Igsf21
|
UTSW |
4 |
139,764,780 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4721:Igsf21
|
UTSW |
4 |
139,834,621 (GRCm39) |
missense |
probably benign |
0.09 |
R4911:Igsf21
|
UTSW |
4 |
139,761,934 (GRCm39) |
missense |
probably benign |
0.01 |
R5157:Igsf21
|
UTSW |
4 |
139,755,378 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5725:Igsf21
|
UTSW |
4 |
139,762,054 (GRCm39) |
missense |
probably benign |
0.02 |
R5778:Igsf21
|
UTSW |
4 |
139,764,832 (GRCm39) |
missense |
probably benign |
0.28 |
R5804:Igsf21
|
UTSW |
4 |
139,755,385 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6140:Igsf21
|
UTSW |
4 |
139,834,684 (GRCm39) |
missense |
probably benign |
0.10 |
R6778:Igsf21
|
UTSW |
4 |
139,761,959 (GRCm39) |
missense |
probably benign |
0.05 |
R6888:Igsf21
|
UTSW |
4 |
139,762,054 (GRCm39) |
missense |
probably benign |
0.02 |
R6963:Igsf21
|
UTSW |
4 |
139,755,041 (GRCm39) |
missense |
probably benign |
0.02 |
R7203:Igsf21
|
UTSW |
4 |
139,834,648 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7485:Igsf21
|
UTSW |
4 |
139,755,049 (GRCm39) |
missense |
probably benign |
0.09 |
R7880:Igsf21
|
UTSW |
4 |
139,884,819 (GRCm39) |
missense |
probably damaging |
1.00 |
R7934:Igsf21
|
UTSW |
4 |
139,761,755 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8175:Igsf21
|
UTSW |
4 |
139,755,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R9035:Igsf21
|
UTSW |
4 |
139,884,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R9190:Igsf21
|
UTSW |
4 |
139,756,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R9197:Igsf21
|
UTSW |
4 |
139,762,084 (GRCm39) |
missense |
probably benign |
0.01 |
R9325:Igsf21
|
UTSW |
4 |
139,794,466 (GRCm39) |
missense |
probably damaging |
0.98 |
R9398:Igsf21
|
UTSW |
4 |
139,973,762 (GRCm39) |
start gained |
probably benign |
|
R9556:Igsf21
|
UTSW |
4 |
139,762,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R9777:Igsf21
|
UTSW |
4 |
139,755,407 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Igsf21
|
UTSW |
4 |
139,794,526 (GRCm39) |
missense |
probably damaging |
1.00 |
|