Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb11 |
C |
T |
2: 69,285,295 |
R575Q |
probably damaging |
Het |
AI464131 |
C |
A |
4: 41,498,407 |
E408* |
probably null |
Het |
Arhgap22 |
T |
G |
14: 33,366,693 |
V377G |
probably benign |
Het |
Asic4 |
T |
C |
1: 75,450,839 |
I3T |
probably damaging |
Het |
Atp2b4 |
T |
C |
1: 133,728,768 |
T715A |
probably benign |
Het |
Ccdc180 |
A |
T |
4: 45,917,508 |
H283L |
probably damaging |
Het |
Cfb |
A |
G |
17: 34,859,026 |
V976A |
probably damaging |
Het |
Cltc |
T |
C |
11: 86,705,163 |
T1250A |
probably damaging |
Het |
Dcbld1 |
T |
A |
10: 52,304,634 |
D131E |
probably damaging |
Het |
Dmxl1 |
T |
C |
18: 49,893,584 |
S1920P |
probably damaging |
Het |
Dnajc13 |
G |
A |
9: 104,230,986 |
H197Y |
probably benign |
Het |
Dpy19l1 |
C |
T |
9: 24,438,628 |
|
probably null |
Het |
Ears2 |
A |
G |
7: 122,044,460 |
|
probably benign |
Het |
Epgn |
A |
C |
5: 91,028,277 |
|
probably benign |
Het |
Ern1 |
T |
C |
11: 106,411,775 |
T418A |
probably benign |
Het |
F12 |
G |
A |
13: 55,420,168 |
P476S |
probably benign |
Het |
Gal3st2c |
C |
T |
1: 94,009,208 |
Q292* |
probably null |
Het |
Galnt7 |
C |
A |
8: 57,584,027 |
Q109H |
possibly damaging |
Het |
Gimap1 |
G |
T |
6: 48,743,098 |
G215W |
probably damaging |
Het |
Gm28042 |
T |
A |
2: 120,041,601 |
|
probably null |
Het |
Gm5414 |
A |
G |
15: 101,625,817 |
I284T |
possibly damaging |
Het |
Hddc3 |
A |
G |
7: 80,343,166 |
E10G |
probably damaging |
Het |
Hmgxb3 |
T |
C |
18: 61,172,194 |
K31E |
probably damaging |
Het |
Hspg2 |
A |
C |
4: 137,518,772 |
Y989S |
probably damaging |
Het |
Kif12 |
G |
A |
4: 63,167,904 |
T402M |
probably benign |
Het |
Klhdc4 |
A |
T |
8: 121,813,790 |
L115* |
probably null |
Het |
Lama2 |
C |
T |
10: 27,190,703 |
V1061M |
possibly damaging |
Het |
Llgl1 |
C |
T |
11: 60,712,007 |
T836I |
possibly damaging |
Het |
Maats1 |
A |
G |
16: 38,332,321 |
S176P |
probably benign |
Het |
Map4k4 |
A |
G |
1: 39,986,762 |
D304G |
probably damaging |
Het |
Matn2 |
A |
G |
15: 34,433,514 |
Q915R |
possibly damaging |
Het |
Myo18a |
A |
G |
11: 77,864,842 |
|
probably benign |
Het |
Nbn |
A |
T |
4: 15,965,132 |
|
probably null |
Het |
Nek8 |
G |
A |
11: 78,170,471 |
Q383* |
probably null |
Het |
Nme7 |
T |
G |
1: 164,380,676 |
Y304* |
probably null |
Het |
Nol8 |
A |
T |
13: 49,661,112 |
H214L |
probably benign |
Het |
Nostrin |
A |
T |
2: 69,175,754 |
I261F |
possibly damaging |
Het |
Olfr46 |
A |
G |
7: 140,610,189 |
T8A |
probably benign |
Het |
Olfr592 |
A |
T |
7: 103,187,503 |
I301L |
probably benign |
Het |
Oprk1 |
T |
G |
1: 5,602,674 |
C345G |
probably damaging |
Het |
Polrmt |
T |
C |
10: 79,737,476 |
S998G |
probably benign |
Het |
Ppp1r12c |
T |
A |
7: 4,484,496 |
R393* |
probably null |
Het |
Prpf3 |
T |
A |
3: 95,849,724 |
|
probably benign |
Het |
Rabl6 |
T |
C |
2: 25,585,373 |
M563V |
probably benign |
Het |
Rasa2 |
C |
A |
9: 96,544,791 |
E775* |
probably null |
Het |
Rc3h1 |
G |
T |
1: 160,951,652 |
V552L |
probably damaging |
Het |
Rhot1 |
A |
T |
11: 80,246,766 |
N365Y |
possibly damaging |
Het |
Rimbp3 |
G |
A |
16: 17,209,917 |
V402M |
possibly damaging |
Het |
Rusc2 |
A |
T |
4: 43,421,805 |
|
probably null |
Het |
Slc25a11 |
T |
C |
11: 70,645,817 |
E141G |
probably damaging |
Het |
Slc34a1 |
A |
T |
13: 55,401,162 |
I142F |
probably damaging |
Het |
Socs6 |
A |
C |
18: 88,869,380 |
Y470* |
probably null |
Het |
Sox12 |
A |
T |
2: 152,397,178 |
L174Q |
unknown |
Het |
Srl |
A |
G |
16: 4,496,403 |
|
probably null |
Het |
Tacc1 |
A |
T |
8: 25,201,221 |
V22E |
probably damaging |
Het |
Thsd7a |
A |
T |
6: 12,379,583 |
C947* |
probably null |
Het |
Tlr12 |
A |
C |
4: 128,618,376 |
V27G |
probably damaging |
Het |
Tmprss4 |
C |
A |
9: 45,173,962 |
V398L |
probably benign |
Het |
Trip6 |
T |
C |
5: 137,312,172 |
D270G |
probably damaging |
Het |
Uba5 |
T |
G |
9: 104,049,298 |
N355T |
probably benign |
Het |
Ubr5 |
A |
G |
15: 38,006,517 |
Y1171H |
probably benign |
Het |
Uhrf1bp1 |
T |
C |
17: 27,885,018 |
L464P |
possibly damaging |
Het |
Vmn2r57 |
A |
G |
7: 41,400,240 |
I695T |
probably benign |
Het |
Vmn2r68 |
T |
A |
7: 85,221,991 |
I695L |
probably damaging |
Het |
Vmn2r79 |
T |
A |
7: 87,001,969 |
M192K |
probably damaging |
Het |
Vps16 |
G |
T |
2: 130,443,368 |
E782* |
probably null |
Het |
Zfp783 |
A |
G |
6: 47,946,803 |
|
noncoding transcript |
Het |
|