Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1500015O10Rik |
G |
A |
1: 43,737,252 |
|
probably null |
Het |
Abhd2 |
T |
C |
7: 79,325,487 |
Y142H |
probably damaging |
Het |
Abra |
C |
T |
15: 41,869,224 |
D149N |
probably benign |
Het |
Acin1 |
A |
T |
14: 54,653,443 |
|
probably benign |
Het |
Adap2 |
T |
A |
11: 80,174,073 |
|
probably null |
Het |
Afdn |
A |
G |
17: 13,888,820 |
E1535G |
probably damaging |
Het |
Ak9 |
A |
G |
10: 41,406,891 |
N1218D |
possibly damaging |
Het |
Angptl1 |
G |
A |
1: 156,844,924 |
V107M |
probably damaging |
Het |
Arhgap26 |
G |
A |
18: 38,899,841 |
|
probably benign |
Het |
Cage1 |
A |
C |
13: 38,025,501 |
S61A |
possibly damaging |
Het |
Cdadc1 |
T |
C |
14: 59,586,555 |
T163A |
probably benign |
Het |
Celsr2 |
A |
T |
3: 108,395,216 |
V2568D |
possibly damaging |
Het |
Cep44 |
G |
A |
8: 56,542,916 |
T166M |
probably damaging |
Het |
Cnksr3 |
T |
C |
10: 7,126,182 |
K187E |
possibly damaging |
Het |
Cyp20a1 |
A |
G |
1: 60,376,099 |
T295A |
probably benign |
Het |
Dus2 |
T |
A |
8: 106,030,442 |
M88K |
probably damaging |
Het |
E330034G19Rik |
A |
T |
14: 24,296,002 |
|
probably benign |
Het |
Efna5 |
T |
C |
17: 62,651,045 |
D72G |
probably benign |
Het |
Epb41l2 |
T |
C |
10: 25,502,140 |
|
probably null |
Het |
Espn |
A |
G |
4: 152,131,252 |
S408P |
probably damaging |
Het |
Evi5l |
T |
C |
8: 4,202,909 |
|
probably benign |
Het |
F830016B08Rik |
G |
A |
18: 60,300,867 |
V341I |
probably benign |
Het |
Flii |
A |
G |
11: 60,716,111 |
L1013P |
possibly damaging |
Het |
Fndc10 |
G |
A |
4: 155,694,807 |
V103M |
probably damaging |
Het |
Frem3 |
T |
A |
8: 80,669,191 |
|
probably null |
Het |
Gltp |
C |
T |
5: 114,674,127 |
R106Q |
probably damaging |
Het |
Gm996 |
G |
A |
2: 25,578,400 |
P500S |
probably damaging |
Het |
Gtf3c3 |
A |
G |
1: 54,419,416 |
Y449H |
probably damaging |
Het |
Hils1 |
G |
A |
11: 94,968,160 |
V94M |
probably damaging |
Het |
Hmga1b |
T |
C |
11: 120,763,040 |
V51A |
probably damaging |
Het |
Hsph1 |
A |
G |
5: 149,618,843 |
V705A |
probably benign |
Het |
Igkv13-84 |
T |
C |
6: 68,939,799 |
S27P |
possibly damaging |
Het |
Il15ra |
A |
G |
2: 11,718,329 |
N55D |
possibly damaging |
Het |
Kctd19 |
T |
G |
8: 105,396,471 |
N104H |
probably damaging |
Het |
Kif27 |
T |
G |
13: 58,331,013 |
D572A |
probably benign |
Het |
Larp1b |
G |
A |
3: 40,963,989 |
G22R |
possibly damaging |
Het |
Lcn2 |
A |
T |
2: 32,384,643 |
|
probably benign |
Het |
Lmtk2 |
T |
A |
5: 144,174,934 |
I824N |
probably benign |
Het |
Ltbp2 |
A |
G |
12: 84,809,348 |
I707T |
probably damaging |
Het |
Macf1 |
A |
G |
4: 123,372,348 |
|
probably null |
Het |
Magel2 |
A |
T |
7: 62,377,738 |
H130L |
unknown |
Het |
Mcoln1 |
A |
G |
8: 3,505,923 |
I73V |
probably damaging |
Het |
Mycbp2 |
G |
T |
14: 103,219,979 |
T1627K |
probably benign |
Het |
Myh8 |
A |
G |
11: 67,286,258 |
E412G |
probably damaging |
Het |
Myo9a |
T |
A |
9: 59,871,072 |
D1370E |
probably benign |
Het |
Ndufaf5 |
A |
G |
2: 140,183,925 |
T135A |
probably benign |
Het |
Neb |
G |
A |
2: 52,271,039 |
Q2207* |
probably null |
Het |
Nek3 |
T |
C |
8: 22,157,039 |
Y160C |
probably damaging |
Het |
Olfr1371 |
G |
C |
11: 52,213,879 |
L37V |
probably benign |
Het |
Olfr175-ps1 |
A |
T |
16: 58,824,106 |
I201N |
possibly damaging |
Het |
Osbpl8 |
A |
G |
10: 111,269,418 |
I245V |
probably benign |
Het |
Pcdh9 |
T |
C |
14: 93,887,643 |
I241V |
probably benign |
Het |
Pcdhb12 |
A |
G |
18: 37,437,160 |
Q453R |
probably benign |
Het |
Pcdhb2 |
A |
G |
18: 37,295,927 |
T318A |
probably benign |
Het |
Prlr |
T |
A |
15: 10,319,376 |
|
probably benign |
Het |
Ptprz1 |
C |
T |
6: 23,001,454 |
A1181V |
possibly damaging |
Het |
Racgap1 |
C |
A |
15: 99,626,206 |
S440I |
probably benign |
Het |
Rap1gap2 |
A |
G |
11: 74,435,699 |
|
probably null |
Het |
Rbm5 |
A |
G |
9: 107,754,146 |
V244A |
probably damaging |
Het |
Rexo5 |
T |
G |
7: 119,819,499 |
I254R |
probably benign |
Het |
Robo2 |
A |
T |
16: 73,985,933 |
S316T |
probably benign |
Het |
Satb2 |
A |
T |
1: 56,845,619 |
V382E |
probably damaging |
Het |
Scg2 |
C |
T |
1: 79,436,664 |
R114Q |
probably benign |
Het |
Scube2 |
T |
C |
7: 109,800,650 |
D893G |
possibly damaging |
Het |
Snrpn |
T |
C |
7: 59,987,526 |
D14G |
possibly damaging |
Het |
Spag17 |
A |
G |
3: 100,103,243 |
T2018A |
probably benign |
Het |
Spata9 |
T |
G |
13: 75,967,882 |
F17V |
possibly damaging |
Het |
Supt6 |
A |
G |
11: 78,212,746 |
Y1378H |
possibly damaging |
Het |
Thsd7b |
T |
C |
1: 129,430,915 |
S29P |
possibly damaging |
Het |
Tmem59 |
A |
T |
4: 107,190,718 |
|
probably benign |
Het |
Tmem87a |
A |
G |
2: 120,397,424 |
S81P |
probably benign |
Het |
Togaram1 |
A |
T |
12: 64,982,450 |
E882D |
possibly damaging |
Het |
Trbj2-4 |
T |
A |
6: 41,543,374 |
|
probably benign |
Het |
Trim42 |
T |
A |
9: 97,363,148 |
Y533F |
probably benign |
Het |
Tssk5 |
C |
T |
15: 76,372,468 |
R280Q |
probably benign |
Het |
Vmn1r82 |
A |
G |
7: 12,305,336 |
T179A |
possibly damaging |
Het |
Yipf7 |
T |
A |
5: 69,519,361 |
Q145L |
possibly damaging |
Het |
|