Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alcam |
A |
C |
16: 52,109,190 (GRCm39) |
|
probably null |
Het |
Ankle2 |
A |
G |
5: 110,401,759 (GRCm39) |
Y807C |
probably damaging |
Het |
Arhgef26 |
A |
C |
3: 62,336,335 (GRCm39) |
M625L |
probably damaging |
Het |
Aspdh |
G |
A |
7: 44,116,474 (GRCm39) |
A86T |
probably damaging |
Het |
Atl1 |
G |
T |
12: 70,006,199 (GRCm39) |
E502* |
probably null |
Het |
Atp6v1c1 |
T |
C |
15: 38,677,790 (GRCm39) |
F105S |
probably damaging |
Het |
Auh |
C |
A |
13: 53,083,446 (GRCm39) |
G17C |
probably benign |
Het |
Ccdc81 |
T |
C |
7: 89,525,352 (GRCm39) |
Y474C |
probably damaging |
Het |
Ccdc82 |
T |
C |
9: 13,251,659 (GRCm39) |
|
probably benign |
Het |
Ccdc96 |
T |
G |
5: 36,643,707 (GRCm39) |
V571G |
probably damaging |
Het |
Col6a5 |
C |
A |
9: 105,814,544 (GRCm39) |
E489D |
unknown |
Het |
Dchs2 |
T |
A |
3: 83,176,577 (GRCm39) |
I845N |
probably damaging |
Het |
Dnajc11 |
T |
C |
4: 152,063,751 (GRCm39) |
V449A |
probably damaging |
Het |
Ect2 |
A |
T |
3: 27,193,268 (GRCm39) |
Y269* |
probably null |
Het |
Egfr |
T |
C |
11: 16,819,294 (GRCm39) |
Y275H |
probably benign |
Het |
Fan1 |
T |
A |
7: 64,004,129 (GRCm39) |
D779V |
probably damaging |
Het |
Fancm |
T |
C |
12: 65,123,942 (GRCm39) |
V200A |
probably damaging |
Het |
Frem1 |
A |
G |
4: 82,884,253 (GRCm39) |
I1214T |
probably benign |
Het |
Gm3415 |
T |
A |
5: 146,494,752 (GRCm39) |
F138L |
probably benign |
Het |
Gtse1 |
C |
A |
15: 85,759,370 (GRCm39) |
T626K |
probably benign |
Het |
Herc1 |
T |
A |
9: 66,393,464 (GRCm39) |
H4114Q |
probably damaging |
Het |
Ifi44 |
T |
A |
3: 151,454,826 (GRCm39) |
N133I |
probably benign |
Het |
Ilf3 |
A |
G |
9: 21,314,447 (GRCm39) |
|
probably benign |
Het |
Inpp4a |
A |
G |
1: 37,437,919 (GRCm39) |
T593A |
probably damaging |
Het |
Iqgap2 |
A |
T |
13: 95,819,441 (GRCm39) |
W634R |
possibly damaging |
Het |
Kcnh4 |
T |
A |
11: 100,641,105 (GRCm39) |
N448I |
probably damaging |
Het |
Klhl33 |
G |
A |
14: 51,130,564 (GRCm39) |
A310V |
probably damaging |
Het |
Klra9 |
G |
T |
6: 130,155,995 (GRCm39) |
Y253* |
probably null |
Het |
Lrig2 |
T |
C |
3: 104,398,863 (GRCm39) |
K222E |
possibly damaging |
Het |
Manba |
G |
A |
3: 135,217,734 (GRCm39) |
|
probably null |
Het |
Mga |
A |
T |
2: 119,754,419 (GRCm39) |
Q976L |
probably damaging |
Het |
Mtmr4 |
A |
G |
11: 87,504,309 (GRCm39) |
D1086G |
probably damaging |
Het |
Muc20 |
A |
G |
16: 32,615,176 (GRCm39) |
V67A |
probably benign |
Het |
Myh3 |
T |
A |
11: 66,973,193 (GRCm39) |
L97Q |
probably damaging |
Het |
Npat |
A |
T |
9: 53,474,739 (GRCm39) |
I844L |
possibly damaging |
Het |
Nrxn3 |
T |
C |
12: 88,762,285 (GRCm39) |
F111L |
probably benign |
Het |
Obp2b |
T |
C |
2: 25,628,599 (GRCm39) |
Y118H |
probably damaging |
Het |
Or5w1 |
T |
A |
2: 87,486,558 (GRCm39) |
K236* |
probably null |
Het |
Or7e170 |
A |
T |
9: 19,795,141 (GRCm39) |
Y153* |
probably null |
Het |
Patj |
A |
G |
4: 98,379,866 (GRCm39) |
D215G |
probably damaging |
Het |
Pex1 |
T |
A |
5: 3,680,196 (GRCm39) |
Y979* |
probably null |
Het |
Septin3 |
G |
A |
15: 82,163,804 (GRCm39) |
V54I |
possibly damaging |
Het |
Shc3 |
A |
G |
13: 51,603,326 (GRCm39) |
Y260H |
probably damaging |
Het |
Simc1 |
A |
G |
13: 54,674,477 (GRCm39) |
T942A |
probably benign |
Het |
Slco1c1 |
T |
C |
6: 141,493,576 (GRCm39) |
S371P |
probably damaging |
Het |
Snrnp200 |
T |
A |
2: 127,080,574 (GRCm39) |
I2029N |
probably damaging |
Het |
Syne1 |
A |
G |
10: 5,268,422 (GRCm39) |
V2089A |
probably benign |
Het |
Syne2 |
T |
C |
12: 76,088,230 (GRCm39) |
S5016P |
probably damaging |
Het |
Tril |
G |
C |
6: 53,795,493 (GRCm39) |
D576E |
probably damaging |
Het |
Tubb2b |
C |
T |
13: 34,311,561 (GRCm39) |
A411T |
probably damaging |
Het |
Ubr4 |
T |
C |
4: 139,156,949 (GRCm39) |
Y2325H |
probably damaging |
Het |
Utp20 |
A |
T |
10: 88,608,395 (GRCm39) |
C1547* |
probably null |
Het |
Utrn |
A |
T |
10: 12,401,171 (GRCm39) |
W98R |
probably damaging |
Het |
Vps35 |
C |
T |
8: 86,000,124 (GRCm39) |
D501N |
possibly damaging |
Het |
Wdr48 |
T |
C |
9: 119,745,879 (GRCm39) |
S421P |
possibly damaging |
Het |
Yju2b |
A |
G |
8: 84,989,630 (GRCm39) |
I63T |
probably damaging |
Het |
Zfp719 |
C |
A |
7: 43,240,412 (GRCm39) |
H667N |
probably damaging |
Het |
|
Other mutations in Nars1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01012:Nars1
|
APN |
18 |
64,638,039 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01962:Nars1
|
APN |
18 |
64,643,554 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01968:Nars1
|
APN |
18 |
64,640,929 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02288:Nars1
|
APN |
18 |
64,643,606 (GRCm39) |
splice site |
probably benign |
|
IGL02366:Nars1
|
APN |
18 |
64,636,599 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL02948:Nars1
|
APN |
18 |
64,638,266 (GRCm39) |
missense |
possibly damaging |
0.66 |
FR4976:Nars1
|
UTSW |
18 |
64,643,516 (GRCm39) |
critical splice donor site |
probably benign |
|
R0591:Nars1
|
UTSW |
18 |
64,633,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R1654:Nars1
|
UTSW |
18 |
64,645,120 (GRCm39) |
missense |
probably damaging |
1.00 |
R1691:Nars1
|
UTSW |
18 |
64,649,485 (GRCm39) |
critical splice donor site |
probably null |
|
R1954:Nars1
|
UTSW |
18 |
64,633,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R2006:Nars1
|
UTSW |
18 |
64,638,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R2516:Nars1
|
UTSW |
18 |
64,638,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R3433:Nars1
|
UTSW |
18 |
64,642,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R4378:Nars1
|
UTSW |
18 |
64,634,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R4667:Nars1
|
UTSW |
18 |
64,638,302 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4737:Nars1
|
UTSW |
18 |
64,649,498 (GRCm39) |
missense |
probably benign |
|
R4877:Nars1
|
UTSW |
18 |
64,633,643 (GRCm39) |
nonsense |
probably null |
|
R5950:Nars1
|
UTSW |
18 |
64,643,556 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6920:Nars1
|
UTSW |
18 |
64,634,471 (GRCm39) |
missense |
probably damaging |
0.99 |
R7082:Nars1
|
UTSW |
18 |
64,637,425 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7132:Nars1
|
UTSW |
18 |
64,640,841 (GRCm39) |
critical splice donor site |
probably null |
|
R7504:Nars1
|
UTSW |
18 |
64,645,093 (GRCm39) |
missense |
probably benign |
0.22 |
R8120:Nars1
|
UTSW |
18 |
64,637,422 (GRCm39) |
missense |
probably benign |
0.19 |
R8343:Nars1
|
UTSW |
18 |
64,637,458 (GRCm39) |
missense |
probably benign |
0.01 |
R8429:Nars1
|
UTSW |
18 |
64,634,391 (GRCm39) |
missense |
probably damaging |
1.00 |
R8929:Nars1
|
UTSW |
18 |
64,644,895 (GRCm39) |
missense |
probably benign |
|
R9321:Nars1
|
UTSW |
18 |
64,637,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R9397:Nars1
|
UTSW |
18 |
64,642,327 (GRCm39) |
missense |
probably benign |
0.30 |
|