Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2410002F23Rik |
T |
A |
7: 44,251,253 |
V194E |
possibly damaging |
Het |
Adgrv1 |
T |
C |
13: 81,413,177 |
N5406S |
probably damaging |
Het |
Asb7 |
T |
A |
7: 66,679,184 |
Q36L |
probably benign |
Het |
Bbof1 |
G |
A |
12: 84,411,217 |
M85I |
probably benign |
Het |
Bin1 |
T |
G |
18: 32,406,145 |
F44V |
probably damaging |
Het |
Bnc2 |
C |
A |
4: 84,292,336 |
V599L |
probably benign |
Het |
Bnip3l |
A |
G |
14: 66,989,202 |
S181P |
probably damaging |
Het |
Btnl9 |
A |
G |
11: 49,175,615 |
L374P |
probably benign |
Het |
Cd109 |
T |
C |
9: 78,664,351 |
I424T |
probably benign |
Het |
Cdhr2 |
G |
A |
13: 54,734,222 |
V1162M |
probably damaging |
Het |
Dgkb |
G |
A |
12: 38,124,217 |
E181K |
probably benign |
Het |
Dnase1 |
A |
T |
16: 4,037,997 |
D64V |
probably damaging |
Het |
E130308A19Rik |
T |
C |
4: 59,719,767 |
I433T |
probably damaging |
Het |
Ecsit |
C |
T |
9: 22,076,296 |
R149H |
probably benign |
Het |
Enpep |
A |
T |
3: 129,305,516 |
V437E |
probably damaging |
Het |
Esrp1 |
A |
T |
4: 11,338,767 |
V679D |
probably damaging |
Het |
Fa2h |
T |
A |
8: 111,348,185 |
|
probably null |
Het |
Fabp1 |
G |
A |
6: 71,199,972 |
E16K |
probably damaging |
Het |
Fstl5 |
T |
A |
3: 76,707,503 |
S624T |
probably benign |
Het |
Gemin5 |
G |
A |
11: 58,128,860 |
R1128W |
probably benign |
Het |
Gm8300 |
G |
A |
12: 87,517,141 |
R82Q |
possibly damaging |
Het |
Hist1h2bg |
T |
C |
13: 23,571,667 |
S79P |
probably damaging |
Het |
Hps3 |
T |
C |
3: 20,003,328 |
H896R |
probably benign |
Het |
Hsf1 |
T |
A |
15: 76,498,281 |
I284K |
probably benign |
Het |
Igkv3-2 |
T |
A |
6: 70,699,004 |
I99N |
probably damaging |
Het |
Iqub |
T |
A |
6: 24,503,785 |
I163F |
possibly damaging |
Het |
Jak2 |
T |
C |
19: 29,298,332 |
I724T |
probably damaging |
Het |
Kbtbd3 |
A |
T |
9: 4,330,408 |
T261S |
probably benign |
Het |
Kctd20 |
G |
T |
17: 28,952,758 |
|
probably null |
Het |
Kif28 |
C |
T |
1: 179,709,449 |
V490M |
probably benign |
Het |
Kif9 |
T |
C |
9: 110,519,140 |
L677P |
probably damaging |
Het |
Klhl18 |
T |
C |
9: 110,428,761 |
Y537C |
probably damaging |
Het |
Mut |
T |
A |
17: 40,943,893 |
I331K |
probably benign |
Het |
Myo5a |
T |
A |
9: 75,181,946 |
S1119R |
probably damaging |
Het |
Napepld |
C |
A |
5: 21,665,321 |
E366D |
probably benign |
Het |
Nbea |
A |
G |
3: 55,987,981 |
V1540A |
probably damaging |
Het |
Neb |
T |
A |
2: 52,221,726 |
I130L |
probably benign |
Het |
Olfr130 |
T |
C |
17: 38,067,479 |
S103P |
probably damaging |
Het |
Olfr18 |
C |
T |
9: 20,314,645 |
D92N |
probably damaging |
Het |
Olfr458 |
A |
T |
6: 42,460,830 |
L63H |
probably damaging |
Het |
Opcml |
T |
C |
9: 28,813,344 |
V146A |
probably damaging |
Het |
Pappa2 |
A |
C |
1: 158,848,400 |
C925W |
probably damaging |
Het |
Parp12 |
T |
A |
6: 39,089,104 |
N562Y |
probably damaging |
Het |
Patj |
C |
A |
4: 98,538,964 |
H1198Q |
probably benign |
Het |
Pcyox1 |
T |
A |
6: 86,389,146 |
K362M |
possibly damaging |
Het |
Pcyt2 |
T |
C |
11: 120,610,939 |
Y350C |
probably benign |
Het |
Pkd1 |
A |
T |
17: 24,565,643 |
T388S |
probably benign |
Het |
Prl3d1 |
T |
A |
13: 27,100,028 |
Y193* |
probably null |
Het |
Psme1 |
A |
T |
14: 55,579,599 |
D15V |
possibly damaging |
Het |
Qrsl1 |
G |
A |
10: 43,874,635 |
R476C |
probably damaging |
Het |
Ranbp2 |
A |
G |
10: 58,479,619 |
N2054D |
probably damaging |
Het |
Serpinb1c |
T |
A |
13: 32,882,069 |
K298* |
probably null |
Het |
Slc22a27 |
A |
T |
19: 7,880,167 |
M355K |
probably benign |
Het |
Spp1 |
T |
A |
5: 104,440,414 |
H227Q |
probably benign |
Het |
Stam2 |
T |
A |
2: 52,719,773 |
N75I |
probably damaging |
Het |
Tacc1 |
T |
C |
8: 25,169,214 |
T579A |
probably benign |
Het |
Tbx3 |
A |
G |
5: 119,683,067 |
D734G |
probably benign |
Het |
Tmem233 |
G |
T |
5: 116,083,082 |
S35* |
probably null |
Het |
Trim43c |
A |
T |
9: 88,840,337 |
E12V |
probably damaging |
Het |
Trio |
A |
G |
15: 27,891,454 |
S463P |
unknown |
Het |
Uggt2 |
A |
T |
14: 119,026,422 |
D1065E |
probably damaging |
Het |
Usp1 |
A |
G |
4: 98,928,913 |
N114S |
probably benign |
Het |
Usp34 |
A |
G |
11: 23,446,787 |
E2377G |
|
Het |
Virma |
T |
A |
4: 11,528,643 |
H1243Q |
probably benign |
Het |
Vmn2r3 |
A |
T |
3: 64,271,293 |
V517D |
probably damaging |
Het |
Zfp931 |
T |
C |
2: 178,068,096 |
K166E |
probably damaging |
Het |
Zp3 |
T |
A |
5: 135,982,750 |
Y141N |
probably damaging |
Het |
|