Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
G |
11: 9,314,491 |
I2958V |
possibly damaging |
Het |
Adam21 |
C |
A |
12: 81,560,352 |
W212L |
probably benign |
Het |
Adcy2 |
A |
C |
13: 68,727,945 |
H479Q |
possibly damaging |
Het |
Adcy4 |
T |
C |
14: 55,781,597 |
R168G |
probably benign |
Het |
Atp13a2 |
T |
C |
4: 141,006,929 |
|
probably benign |
Het |
C1ra |
G |
A |
6: 124,517,505 |
E304K |
possibly damaging |
Het |
C87977 |
A |
G |
4: 144,209,340 |
|
probably null |
Het |
Cc2d2a |
A |
C |
5: 43,681,381 |
|
probably benign |
Het |
Cenpe |
T |
C |
3: 135,246,827 |
L1426P |
probably damaging |
Het |
Cntn1 |
A |
T |
15: 92,314,563 |
R869* |
probably null |
Het |
Creb3l2 |
A |
T |
6: 37,334,348 |
|
probably benign |
Het |
Crybg2 |
G |
A |
4: 134,075,304 |
|
probably benign |
Het |
Csmd1 |
A |
T |
8: 16,226,391 |
F800I |
probably damaging |
Het |
Dock6 |
G |
A |
9: 21,841,527 |
T330I |
probably damaging |
Het |
Ets2 |
G |
A |
16: 95,716,156 |
E311K |
possibly damaging |
Het |
Fbxo22 |
A |
T |
9: 55,214,960 |
Q141L |
probably benign |
Het |
Fer |
C |
T |
17: 64,035,508 |
T223M |
probably benign |
Het |
Gm13757 |
A |
T |
2: 88,446,617 |
M107K |
probably benign |
Het |
Gm9774 |
C |
T |
3: 92,428,809 |
W125* |
probably null |
Het |
Gtf3c1 |
A |
T |
7: 125,657,477 |
|
probably benign |
Het |
Gtf3c2 |
G |
A |
5: 31,159,806 |
R684* |
probably null |
Het |
Hs6st3 |
T |
A |
14: 119,869,062 |
L294* |
probably null |
Het |
Ighg2c |
T |
G |
12: 113,287,964 |
E181A |
unknown |
Het |
Igkv6-15 |
A |
T |
6: 70,406,779 |
|
probably benign |
Het |
Lrmp |
A |
T |
6: 145,174,628 |
H523L |
probably damaging |
Het |
Map2k6 |
C |
T |
11: 110,494,343 |
R178* |
probably null |
Het |
Meikin |
T |
A |
11: 54,390,483 |
D126E |
probably benign |
Het |
Mgst1 |
A |
T |
6: 138,156,331 |
T37S |
probably damaging |
Het |
Mrc2 |
G |
A |
11: 105,347,692 |
V1222M |
probably benign |
Het |
Myom2 |
C |
A |
8: 15,119,216 |
|
probably benign |
Het |
Negr1 |
A |
G |
3: 157,016,266 |
K159R |
possibly damaging |
Het |
Nptx1 |
T |
C |
11: 119,543,301 |
T320A |
possibly damaging |
Het |
Olfr490 |
T |
C |
7: 108,286,296 |
I277V |
probably benign |
Het |
Olfr530 |
A |
T |
7: 140,373,397 |
V71E |
possibly damaging |
Het |
Pes1 |
C |
T |
11: 3,977,794 |
|
probably benign |
Het |
Pes1 |
T |
G |
11: 3,977,795 |
|
probably benign |
Het |
Pkhd1 |
A |
T |
1: 20,117,474 |
Y3537N |
probably damaging |
Het |
Rassf5 |
T |
C |
1: 131,244,956 |
R59G |
probably damaging |
Het |
Reln |
A |
T |
5: 22,018,869 |
W961R |
probably damaging |
Het |
Rhot2 |
G |
A |
17: 25,842,028 |
H168Y |
possibly damaging |
Het |
Ripk3 |
G |
T |
14: 55,788,391 |
|
probably benign |
Het |
Samm50 |
A |
G |
15: 84,214,171 |
|
silent |
Het |
Sap30bp |
T |
C |
11: 115,957,403 |
I117T |
probably damaging |
Het |
Sephs1 |
A |
G |
2: 4,899,560 |
T250A |
probably benign |
Het |
Sipa1l2 |
A |
T |
8: 125,422,624 |
L1632* |
probably null |
Het |
Sirt7 |
T |
C |
11: 120,622,129 |
|
probably benign |
Het |
Smg8 |
T |
C |
11: 87,086,108 |
T216A |
possibly damaging |
Het |
Sox9 |
A |
G |
11: 112,784,942 |
Y319C |
probably damaging |
Het |
Sspn |
G |
A |
6: 145,961,151 |
A27T |
possibly damaging |
Het |
Suco |
A |
G |
1: 161,838,804 |
V509A |
possibly damaging |
Het |
Svep1 |
C |
T |
4: 58,070,661 |
C2375Y |
possibly damaging |
Het |
Trbv21 |
T |
A |
6: 41,203,050 |
|
probably benign |
Het |
Uimc1 |
C |
T |
13: 55,060,266 |
E455K |
possibly damaging |
Het |
Upk3b |
A |
G |
5: 136,040,076 |
T100A |
possibly damaging |
Het |
Usp47 |
A |
G |
7: 112,108,655 |
N1303D |
probably damaging |
Het |
Vav1 |
A |
T |
17: 57,303,862 |
D476V |
probably benign |
Het |
Vmn1r68 |
A |
G |
7: 10,527,235 |
V312A |
probably benign |
Het |
Wdr62 |
A |
G |
7: 30,270,174 |
V287A |
probably damaging |
Het |
Zcchc4 |
C |
T |
5: 52,783,208 |
P40S |
probably benign |
Het |
Zfp326 |
T |
A |
5: 105,886,203 |
Y26* |
probably null |
Het |
Zfp592 |
A |
G |
7: 81,038,071 |
H915R |
probably damaging |
Het |
|