Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acaa1a |
A |
G |
9: 119,173,564 (GRCm39) |
M146V |
probably benign |
Het |
Adcy1 |
C |
T |
11: 7,094,762 (GRCm39) |
R563C |
probably damaging |
Het |
Ambn |
A |
T |
5: 88,609,493 (GRCm39) |
Y67F |
possibly damaging |
Het |
Ankrd42 |
T |
A |
7: 92,241,080 (GRCm39) |
E426D |
probably benign |
Het |
Ankzf1 |
A |
G |
1: 75,174,623 (GRCm39) |
T538A |
probably benign |
Het |
Arhgap20 |
A |
G |
9: 51,751,802 (GRCm39) |
I418V |
probably benign |
Het |
Arhgef28 |
A |
G |
13: 98,115,003 (GRCm39) |
Y616H |
probably benign |
Het |
B4galt4 |
T |
C |
16: 38,588,376 (GRCm39) |
F340S |
probably damaging |
Het |
Bmp1 |
C |
T |
14: 70,727,562 (GRCm39) |
E674K |
probably benign |
Het |
Ccr9 |
T |
A |
9: 123,608,534 (GRCm39) |
V72D |
probably damaging |
Het |
Chd2 |
T |
A |
7: 73,101,556 (GRCm39) |
K1390I |
probably damaging |
Het |
Col5a3 |
C |
T |
9: 20,711,585 (GRCm39) |
R513Q |
unknown |
Het |
Cracd |
A |
G |
5: 76,805,905 (GRCm39) |
R126G |
unknown |
Het |
Cttnbp2 |
G |
T |
6: 18,378,419 (GRCm39) |
N1472K |
probably benign |
Het |
Edn3 |
A |
G |
2: 174,621,328 (GRCm39) |
|
probably null |
Het |
Eps15l1 |
A |
G |
8: 73,136,634 (GRCm39) |
F331L |
probably damaging |
Het |
Gm45337 |
CACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCTACAGCCTCC |
CACAGCCTCC |
7: 141,698,021 (GRCm39) |
|
probably benign |
Het |
Lrrc56 |
A |
G |
7: 140,789,443 (GRCm39) |
S487G |
probably benign |
Het |
Moxd2 |
A |
G |
6: 40,868,746 (GRCm39) |
T93A |
probably benign |
Het |
Npr2 |
T |
C |
4: 43,650,415 (GRCm39) |
V970A |
probably damaging |
Het |
Or4a79 |
T |
C |
2: 89,552,281 (GRCm39) |
Y58C |
possibly damaging |
Het |
Or5an10 |
T |
C |
19: 12,276,041 (GRCm39) |
S152G |
probably damaging |
Het |
Or8b9 |
T |
C |
9: 37,766,314 (GRCm39) |
S67P |
probably damaging |
Het |
Or8g28 |
T |
G |
9: 39,169,762 (GRCm39) |
I69L |
probably benign |
Het |
Pacc1 |
A |
G |
1: 191,078,910 (GRCm39) |
|
probably null |
Het |
Pdf |
A |
T |
8: 107,773,781 (GRCm39) |
F221I |
probably damaging |
Het |
Plekhn1 |
A |
C |
4: 156,317,771 (GRCm39) |
S205R |
probably benign |
Het |
Ppp6r1 |
G |
A |
7: 4,639,129 (GRCm39) |
A606V |
probably benign |
Het |
Prpf38b |
C |
T |
3: 108,812,446 (GRCm39) |
V256I |
probably benign |
Het |
Rbbp5 |
T |
A |
1: 132,421,879 (GRCm39) |
H291Q |
probably benign |
Het |
Rnf169 |
T |
C |
7: 99,629,445 (GRCm39) |
E66G |
probably damaging |
Het |
Rp1 |
T |
A |
1: 4,381,501 (GRCm39) |
N328Y |
unknown |
Het |
Skint5 |
A |
T |
4: 113,417,035 (GRCm39) |
V1138E |
unknown |
Het |
Slc27a4 |
T |
C |
2: 29,702,717 (GRCm39) |
V539A |
probably damaging |
Het |
Smo |
G |
T |
6: 29,755,534 (GRCm39) |
R402L |
probably benign |
Het |
Srgap2 |
A |
T |
1: 131,364,569 (GRCm39) |
L4Q |
probably damaging |
Het |
Tbxas1 |
A |
T |
6: 38,959,146 (GRCm39) |
R110* |
probably null |
Het |
Thoc7 |
A |
C |
14: 13,951,204 (GRCm38) |
|
probably null |
Het |
Tmub1 |
G |
A |
5: 24,652,507 (GRCm39) |
|
probably benign |
Het |
Tnrc6a |
A |
G |
7: 122,772,673 (GRCm39) |
|
probably null |
Het |
Traj19 |
T |
A |
14: 54,437,860 (GRCm39) |
H6Q |
unknown |
Het |
Trim30c |
T |
C |
7: 104,036,758 (GRCm39) |
E200G |
probably benign |
Het |
Ubqlnl |
A |
T |
7: 103,798,048 (GRCm39) |
I483N |
probably damaging |
Het |
Usp25 |
G |
T |
16: 76,874,089 (GRCm39) |
R555L |
probably damaging |
Het |
Vgll4 |
A |
G |
6: 114,839,293 (GRCm39) |
S233P |
probably damaging |
Het |
Vps13b |
G |
A |
15: 35,910,670 (GRCm39) |
C3478Y |
possibly damaging |
Het |
Vwa8 |
T |
A |
14: 79,162,686 (GRCm39) |
|
probably null |
Het |
Zfp977 |
A |
G |
7: 42,229,629 (GRCm39) |
Y299H |
probably damaging |
Het |
Zmynd11 |
T |
A |
13: 9,785,434 (GRCm39) |
H17L |
probably benign |
Het |
|
Other mutations in Ngp |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
PIT4131001:Ngp
|
UTSW |
9 |
110,251,337 (GRCm39) |
unclassified |
probably benign |
|
R0230:Ngp
|
UTSW |
9 |
110,249,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R2004:Ngp
|
UTSW |
9 |
110,249,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R4610:Ngp
|
UTSW |
9 |
110,249,883 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5100:Ngp
|
UTSW |
9 |
110,249,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R5762:Ngp
|
UTSW |
9 |
110,251,401 (GRCm39) |
missense |
probably benign |
0.09 |
R6514:Ngp
|
UTSW |
9 |
110,249,017 (GRCm39) |
missense |
probably damaging |
0.98 |
R6791:Ngp
|
UTSW |
9 |
110,249,017 (GRCm39) |
missense |
probably benign |
0.01 |
R7286:Ngp
|
UTSW |
9 |
110,249,978 (GRCm39) |
missense |
probably benign |
0.00 |
R7820:Ngp
|
UTSW |
9 |
110,249,932 (GRCm39) |
missense |
probably benign |
0.04 |
R8119:Ngp
|
UTSW |
9 |
110,251,421 (GRCm39) |
missense |
probably benign |
0.00 |
R9025:Ngp
|
UTSW |
9 |
110,251,451 (GRCm39) |
missense |
possibly damaging |
0.92 |
RF021:Ngp
|
UTSW |
9 |
110,250,824 (GRCm39) |
missense |
possibly damaging |
0.55 |
|