Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930596D02Rik |
A |
T |
14: 35,532,020 (GRCm39) |
L185* |
probably null |
Het |
Actrt3 |
A |
T |
3: 30,653,840 (GRCm39) |
D53E |
probably benign |
Het |
Ankrd34b |
T |
C |
13: 92,575,016 (GRCm39) |
S83P |
probably damaging |
Het |
Asap1 |
A |
G |
15: 63,966,018 (GRCm39) |
V1029A |
probably benign |
Het |
Blk |
T |
C |
14: 63,617,143 (GRCm39) |
E288G |
probably benign |
Het |
Cep192 |
T |
G |
18: 67,967,634 (GRCm39) |
V706G |
probably damaging |
Het |
Chd2 |
T |
C |
7: 73,125,097 (GRCm39) |
K908E |
probably damaging |
Het |
Dnm1l |
A |
T |
16: 16,139,521 (GRCm39) |
I391N |
possibly damaging |
Het |
Fmn1 |
A |
G |
2: 113,355,622 (GRCm39) |
R688G |
unknown |
Het |
Gdap2 |
A |
G |
3: 100,078,336 (GRCm39) |
D100G |
probably benign |
Het |
Gm43638 |
T |
C |
5: 87,610,769 (GRCm39) |
I522V |
possibly damaging |
Het |
Gsap |
A |
T |
5: 21,447,801 (GRCm39) |
|
probably null |
Het |
Hoxd12 |
A |
G |
2: 74,505,905 (GRCm39) |
S159G |
probably benign |
Het |
Ints7 |
A |
G |
1: 191,345,749 (GRCm39) |
|
probably null |
Het |
Iqsec3 |
G |
A |
6: 121,389,900 (GRCm39) |
Q524* |
probably null |
Het |
Klra10 |
T |
A |
6: 130,258,845 (GRCm39) |
H14L |
possibly damaging |
Het |
Lratd1 |
T |
C |
12: 14,200,646 (GRCm39) |
D27G |
probably damaging |
Het |
Mettl15 |
T |
C |
2: 108,961,925 (GRCm39) |
E228G |
probably damaging |
Het |
Or51v8 |
T |
C |
7: 103,319,591 (GRCm39) |
M216V |
probably benign |
Het |
Or9s18 |
G |
A |
13: 65,300,210 (GRCm39) |
M57I |
probably damaging |
Het |
Pabpc1l |
A |
G |
2: 163,873,197 (GRCm39) |
N156D |
probably benign |
Het |
Pkhd1l1 |
G |
T |
15: 44,379,605 (GRCm39) |
|
probably null |
Het |
Pm20d1 |
T |
A |
1: 131,732,697 (GRCm39) |
N345K |
probably benign |
Het |
Rasgrp1 |
A |
G |
2: 117,113,057 (GRCm39) |
V785A |
probably benign |
Het |
Sos2 |
A |
G |
12: 69,643,440 (GRCm39) |
L980S |
probably damaging |
Het |
Stam2 |
A |
T |
2: 52,609,947 (GRCm39) |
H56Q |
probably damaging |
Het |
Trpm6 |
T |
A |
19: 18,779,571 (GRCm39) |
|
probably benign |
Het |
Trpm7 |
A |
T |
2: 126,688,079 (GRCm39) |
D249E |
probably damaging |
Het |
Vmn1r203 |
A |
T |
13: 22,708,539 (GRCm39) |
T107S |
possibly damaging |
Het |
Vmn2r55 |
A |
G |
7: 12,404,887 (GRCm39) |
L172P |
probably damaging |
Het |
Vrtn |
A |
G |
12: 84,696,923 (GRCm39) |
R558G |
probably benign |
Het |
Zfp977 |
A |
T |
7: 42,232,439 (GRCm39) |
D7E |
probably damaging |
Het |
|
Other mutations in Aadacl4fm5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01139:Aadacl4fm5
|
APN |
4 |
144,504,259 (GRCm39) |
nonsense |
probably null |
|
IGL01293:Aadacl4fm5
|
APN |
4 |
144,504,159 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01678:Aadacl4fm5
|
APN |
4 |
144,504,443 (GRCm39) |
missense |
probably benign |
0.20 |
IGL02609:Aadacl4fm5
|
APN |
4 |
144,506,307 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02734:Aadacl4fm5
|
APN |
4 |
144,506,349 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02869:Aadacl4fm5
|
APN |
4 |
144,512,938 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02988:Aadacl4fm5
|
APN |
4 |
144,513,100 (GRCm39) |
utr 5 prime |
probably benign |
|
R0553:Aadacl4fm5
|
UTSW |
4 |
144,503,985 (GRCm39) |
missense |
possibly damaging |
0.57 |
R1514:Aadacl4fm5
|
UTSW |
4 |
144,504,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R1856:Aadacl4fm5
|
UTSW |
4 |
144,504,453 (GRCm39) |
missense |
probably benign |
|
R1957:Aadacl4fm5
|
UTSW |
4 |
144,504,389 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2014:Aadacl4fm5
|
UTSW |
4 |
144,506,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R2243:Aadacl4fm5
|
UTSW |
4 |
144,503,991 (GRCm39) |
missense |
probably benign |
|
R4943:Aadacl4fm5
|
UTSW |
4 |
144,504,290 (GRCm39) |
missense |
probably benign |
0.07 |
R5439:Aadacl4fm5
|
UTSW |
4 |
144,504,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R5520:Aadacl4fm5
|
UTSW |
4 |
144,504,594 (GRCm39) |
missense |
probably benign |
0.00 |
R6414:Aadacl4fm5
|
UTSW |
4 |
144,503,985 (GRCm39) |
missense |
possibly damaging |
0.57 |
R6664:Aadacl4fm5
|
UTSW |
4 |
144,503,969 (GRCm39) |
makesense |
probably null |
|
R6869:Aadacl4fm5
|
UTSW |
4 |
144,507,042 (GRCm39) |
critical splice donor site |
probably null |
|
R7384:Aadacl4fm5
|
UTSW |
4 |
144,507,191 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7439:Aadacl4fm5
|
UTSW |
4 |
144,504,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R7484:Aadacl4fm5
|
UTSW |
4 |
144,504,521 (GRCm39) |
missense |
probably damaging |
0.97 |
R9284:Aadacl4fm5
|
UTSW |
4 |
144,504,191 (GRCm39) |
missense |
probably damaging |
1.00 |
|