Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1a |
A |
T |
5: 8,736,164 (GRCm39) |
I186F |
probably benign |
Het |
Afg3l1 |
T |
C |
8: 124,221,678 (GRCm39) |
|
probably benign |
Het |
Atg4a |
G |
A |
X: 139,893,589 (GRCm39) |
E106K |
probably benign |
Het |
Ccdc50 |
A |
G |
16: 27,225,479 (GRCm39) |
E64G |
probably damaging |
Het |
Celsr3 |
G |
T |
9: 108,706,507 (GRCm39) |
G997W |
probably damaging |
Het |
Chd8 |
C |
T |
14: 52,441,952 (GRCm39) |
E2138K |
possibly damaging |
Het |
Col19a1 |
C |
T |
1: 24,598,762 (GRCm39) |
G77E |
unknown |
Het |
Dnaaf11 |
A |
G |
15: 66,319,525 (GRCm39) |
|
probably benign |
Het |
Fhad1 |
G |
T |
4: 141,632,279 (GRCm39) |
Q1287K |
probably benign |
Het |
Fzr1 |
G |
T |
10: 81,205,252 (GRCm39) |
T159K |
probably damaging |
Het |
Gm10608 |
CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA |
CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA |
9: 118,989,784 (GRCm39) |
|
probably null |
Het |
Gna13 |
T |
C |
11: 109,253,951 (GRCm39) |
I51T |
probably damaging |
Het |
Gorab |
A |
G |
1: 163,224,375 (GRCm39) |
|
probably null |
Het |
Hydin |
T |
C |
8: 111,245,746 (GRCm39) |
V2153A |
probably benign |
Het |
Ints6 |
A |
G |
14: 62,942,275 (GRCm39) |
V486A |
probably damaging |
Het |
Irx2 |
A |
G |
13: 72,779,709 (GRCm39) |
K331R |
probably damaging |
Het |
Mark2 |
T |
C |
19: 7,264,227 (GRCm39) |
E116G |
probably damaging |
Het |
Med14 |
A |
T |
X: 12,550,235 (GRCm39) |
H684Q |
probably benign |
Het |
Or1e25 |
A |
T |
11: 73,494,209 (GRCm39) |
T268S |
probably benign |
Het |
Pde5a |
T |
C |
3: 122,645,357 (GRCm39) |
L755P |
probably damaging |
Het |
Pex14 |
A |
T |
4: 149,047,968 (GRCm39) |
I203N |
probably benign |
Het |
Pi4ka |
T |
C |
16: 17,168,657 (GRCm39) |
E691G |
probably damaging |
Het |
Plekha1 |
G |
T |
7: 130,510,095 (GRCm39) |
W280C |
probably damaging |
Het |
Pnoc |
A |
T |
14: 65,642,284 (GRCm39) |
F160I |
probably damaging |
Het |
Ppfia3 |
C |
A |
7: 45,005,852 (GRCm39) |
R348L |
probably damaging |
Het |
Ppil6 |
A |
T |
10: 41,377,689 (GRCm39) |
|
probably benign |
Het |
Psmd13 |
C |
A |
7: 140,477,653 (GRCm39) |
|
probably benign |
Het |
Psme4 |
T |
C |
11: 30,795,173 (GRCm39) |
|
probably benign |
Het |
Rfx3 |
T |
C |
19: 27,784,186 (GRCm39) |
|
probably benign |
Het |
Rnase11 |
A |
G |
14: 51,287,227 (GRCm39) |
L109S |
probably damaging |
Het |
Rngtt |
A |
G |
4: 33,368,678 (GRCm39) |
T404A |
probably benign |
Het |
Sbf1 |
A |
G |
15: 89,187,421 (GRCm39) |
|
probably null |
Het |
Sema5b |
A |
G |
16: 35,480,301 (GRCm39) |
N656S |
probably damaging |
Het |
Ssh3 |
T |
C |
19: 4,315,324 (GRCm39) |
Y338C |
probably damaging |
Het |
Tgfbr3l |
A |
G |
8: 4,299,280 (GRCm39) |
D49G |
probably damaging |
Het |
Thbs1 |
C |
T |
2: 117,948,109 (GRCm39) |
T423I |
probably benign |
Het |
Ttc17 |
A |
T |
2: 94,206,419 (GRCm39) |
Y243* |
probably null |
Het |
Zbtb8os |
A |
T |
4: 129,235,309 (GRCm39) |
E54D |
probably damaging |
Het |
Zfp648 |
A |
T |
1: 154,080,881 (GRCm39) |
K347* |
probably null |
Het |
Zfp84 |
T |
G |
7: 29,474,758 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Aadacl2fm1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01380:Aadacl2fm1
|
APN |
3 |
59,840,053 (GRCm39) |
missense |
probably benign |
|
IGL02850:Aadacl2fm1
|
APN |
3 |
59,843,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R0099:Aadacl2fm1
|
UTSW |
3 |
59,843,856 (GRCm39) |
missense |
probably benign |
0.00 |
R0206:Aadacl2fm1
|
UTSW |
3 |
59,840,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R0208:Aadacl2fm1
|
UTSW |
3 |
59,840,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R0457:Aadacl2fm1
|
UTSW |
3 |
59,844,054 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0511:Aadacl2fm1
|
UTSW |
3 |
59,843,771 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1824:Aadacl2fm1
|
UTSW |
3 |
59,840,001 (GRCm39) |
nonsense |
probably null |
|
R2567:Aadacl2fm1
|
UTSW |
3 |
59,836,475 (GRCm39) |
splice site |
probably benign |
|
R3826:Aadacl2fm1
|
UTSW |
3 |
59,843,896 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4356:Aadacl2fm1
|
UTSW |
3 |
59,843,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R4755:Aadacl2fm1
|
UTSW |
3 |
59,843,735 (GRCm39) |
missense |
probably benign |
|
R4975:Aadacl2fm1
|
UTSW |
3 |
59,840,161 (GRCm39) |
missense |
probably damaging |
0.98 |
R5199:Aadacl2fm1
|
UTSW |
3 |
59,843,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R7221:Aadacl2fm1
|
UTSW |
3 |
59,836,354 (GRCm39) |
start gained |
probably benign |
|
R7336:Aadacl2fm1
|
UTSW |
3 |
59,840,174 (GRCm39) |
splice site |
probably null |
|
R8150:Aadacl2fm1
|
UTSW |
3 |
59,843,558 (GRCm39) |
missense |
probably damaging |
0.99 |
R8159:Aadacl2fm1
|
UTSW |
3 |
59,843,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R9325:Aadacl2fm1
|
UTSW |
3 |
59,843,862 (GRCm39) |
missense |
probably benign |
0.01 |
R9378:Aadacl2fm1
|
UTSW |
3 |
59,839,110 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9495:Aadacl2fm1
|
UTSW |
3 |
59,840,114 (GRCm39) |
missense |
possibly damaging |
0.87 |
|