Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933416C03Rik |
T |
C |
10: 116,112,535 |
Y362C |
probably benign |
Het |
Aatk |
A |
G |
11: 120,046,920 |
S11P |
unknown |
Het |
Adrb2 |
T |
C |
18: 62,178,933 |
T274A |
probably damaging |
Het |
Aph1b |
A |
G |
9: 66,794,221 |
S45P |
probably damaging |
Het |
Atp9b |
A |
T |
18: 80,844,591 |
D321E |
|
Het |
C1qbp |
A |
G |
11: 70,978,717 |
V180A |
possibly damaging |
Het |
C4b |
G |
T |
17: 34,734,539 |
A990D |
probably damaging |
Het |
Ccdc80 |
T |
A |
16: 45,095,249 |
S123T |
possibly damaging |
Het |
Cdh18 |
A |
C |
15: 23,474,052 |
E669D |
possibly damaging |
Het |
Ceacam3 |
T |
A |
7: 17,161,683 |
V526D |
|
Het |
Cenpf |
C |
T |
1: 189,672,585 |
C349Y |
probably damaging |
Het |
Dmrt2 |
T |
C |
19: 25,678,015 |
V326A |
probably damaging |
Het |
Dock9 |
T |
C |
14: 121,546,042 |
Q2023R |
probably damaging |
Het |
Exd2 |
A |
G |
12: 80,475,997 |
R77G |
probably benign |
Het |
Exph5 |
A |
T |
9: 53,375,848 |
K1410* |
probably null |
Het |
Eya2 |
A |
G |
2: 165,767,068 |
T443A |
probably damaging |
Het |
Fam135a |
G |
A |
1: 24,028,488 |
T1100M |
probably benign |
Het |
Foxp2 |
G |
T |
6: 15,403,867 |
R381L |
unknown |
Het |
Grm7 |
T |
G |
6: 111,080,354 |
V305G |
probably benign |
Het |
Gzma |
G |
A |
13: 113,100,930 |
R8W |
probably benign |
Het |
H6pd |
T |
C |
4: 149,981,676 |
E759G |
probably benign |
Het |
Ift27 |
A |
G |
15: 78,164,191 |
V154A |
probably benign |
Het |
Kif1a |
A |
T |
1: 93,022,419 |
S1429T |
probably benign |
Het |
Lrrn1 |
T |
A |
6: 107,569,333 |
D697E |
probably benign |
Het |
Mcrs1 |
A |
T |
15: 99,243,694 |
I387N |
probably damaging |
Het |
Naf1 |
GCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAACTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAACTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAACTCGGATCCCGGCGGAAGACCACCGCCGCCGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCCGCCAGCCCCGAACTGGGATGCGGGCGGAAGACCACCACCGCCGCCAGCCCCGAACTCGGATCCCGGCGGAAGACC |
GCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAACTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCTGCCAGCCCCGAACTCGGATCCCGGCGGAAGACCACCGCCGCCGCCAGCCCCGAGCTCGGATCCCGGCGGAAGACCACCGCCGCCGCCAGCCCCGAACTGGGATGCGGGCGGAAGACCACCACCGCCGCCAGCCCCGAACTCGGATCCCGGCGGAAGACC |
8: 66,860,548 |
|
probably benign |
Het |
Nid1 |
C |
A |
13: 13,437,831 |
L44I |
possibly damaging |
Het |
Olfr1046 |
T |
A |
2: 86,217,113 |
E199V |
probably damaging |
Het |
Olfr197 |
A |
G |
16: 59,185,754 |
I243T |
unknown |
Het |
Olfr452 |
A |
T |
6: 42,790,710 |
T224S |
possibly damaging |
Het |
Olfr734 |
T |
C |
14: 50,320,776 |
T20A |
probably benign |
Het |
Pde11a |
C |
T |
2: 76,059,010 |
D707N |
probably damaging |
Het |
Pigf |
A |
T |
17: 87,020,482 |
L119* |
probably null |
Het |
Pkd1l1 |
A |
T |
11: 8,870,277 |
C1679* |
probably null |
Het |
Prnp |
A |
G |
2: 131,936,749 |
N107S |
probably benign |
Het |
Ptgfr |
C |
T |
3: 151,835,416 |
V152M |
possibly damaging |
Het |
Rap2b |
A |
G |
3: 61,364,384 |
|
probably benign |
Het |
Rtn4 |
A |
G |
11: 29,707,300 |
T485A |
probably damaging |
Het |
Sec23b |
A |
G |
2: 144,559,314 |
T32A |
probably benign |
Het |
Skint5 |
A |
T |
4: 113,580,482 |
|
probably null |
Het |
Slc13a5 |
A |
G |
11: 72,257,384 |
L275P |
probably damaging |
Het |
Slc20a1 |
C |
T |
2: 129,199,864 |
A49V |
probably damaging |
Het |
Slc35g2 |
A |
G |
9: 100,553,171 |
I149T |
probably benign |
Het |
Syk |
T |
A |
13: 52,624,727 |
I283K |
probably benign |
Het |
Tnfsf13b |
G |
A |
8: 10,006,795 |
|
probably benign |
Het |
Ubr1 |
A |
G |
2: 120,870,995 |
V1592A |
probably benign |
Het |
Vopp1 |
T |
C |
6: 57,762,394 |
*123W |
probably null |
Het |
Xpo4 |
T |
A |
14: 57,604,456 |
Q467H |
probably damaging |
Het |
Zdhhc22 |
A |
C |
12: 86,988,369 |
V103G |
possibly damaging |
Het |
Zfp868 |
A |
G |
8: 69,611,509 |
S392P |
probably damaging |
Het |
|