Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Afap1 |
A |
T |
5: 35,974,525 |
I399F |
possibly damaging |
Het |
Aknad1 |
C |
T |
3: 108,752,387 |
P239L |
probably benign |
Het |
Ankrd9 |
A |
G |
12: 110,976,766 |
V245A |
probably benign |
Het |
Anxa1 |
T |
C |
19: 20,378,493 |
|
probably benign |
Het |
Arhgef2 |
A |
G |
3: 88,636,080 |
K454R |
probably damaging |
Het |
AU040320 |
A |
G |
4: 126,814,271 |
T227A |
probably benign |
Het |
Bbs2 |
C |
T |
8: 94,098,303 |
R17H |
probably damaging |
Het |
Bcl2l12 |
A |
G |
7: 44,991,464 |
|
probably benign |
Het |
C1qtnf9 |
G |
T |
14: 60,772,288 |
|
probably benign |
Het |
Ccdc38 |
C |
G |
10: 93,570,886 |
Y219* |
probably null |
Het |
Ceacam3 |
G |
T |
7: 17,159,745 |
D394Y |
probably damaging |
Het |
Crip1 |
A |
C |
12: 113,153,667 |
|
probably null |
Het |
Dnah9 |
C |
A |
11: 65,834,199 |
C4376F |
probably damaging |
Het |
Fam71f2 |
A |
G |
6: 29,285,943 |
R76G |
probably null |
Het |
Galnt9 |
T |
C |
5: 110,615,466 |
F446L |
probably damaging |
Het |
Gm14322 |
A |
G |
2: 177,769,706 |
D103G |
probably benign |
Het |
Gpa33 |
T |
C |
1: 166,130,538 |
|
probably null |
Het |
Lactb2 |
T |
A |
1: 13,650,730 |
I93F |
probably benign |
Het |
Lifr |
A |
T |
15: 7,159,416 |
T93S |
probably benign |
Het |
Lmbr1l |
A |
T |
15: 98,912,427 |
I101N |
probably damaging |
Het |
Lrrc8c |
G |
A |
5: 105,608,251 |
V631M |
possibly damaging |
Het |
Mctp2 |
A |
C |
7: 72,228,540 |
D263E |
probably damaging |
Het |
Nbeal1 |
T |
A |
1: 60,267,892 |
I1627N |
possibly damaging |
Het |
Neb |
T |
C |
2: 52,197,894 |
Y5188C |
probably damaging |
Het |
Nf1 |
T |
C |
11: 79,569,222 |
|
probably benign |
Het |
Nr6a1 |
T |
C |
2: 38,739,091 |
D250G |
probably damaging |
Het |
Ola1 |
T |
C |
2: 73,156,784 |
E168G |
probably benign |
Het |
Olfr1505 |
T |
A |
19: 13,919,775 |
F252I |
probably damaging |
Het |
Olfr403 |
T |
C |
11: 74,196,118 |
V205A |
probably damaging |
Het |
Olfr715b |
T |
A |
7: 107,106,621 |
Q80L |
probably damaging |
Het |
Olfr730 |
A |
G |
14: 50,186,968 |
I83T |
probably benign |
Het |
Olfr837 |
T |
C |
9: 19,137,388 |
Y132H |
probably damaging |
Het |
Pik3r6 |
C |
T |
11: 68,525,671 |
Q29* |
probably null |
Het |
Ppargc1a |
C |
T |
5: 51,463,237 |
|
probably benign |
Het |
Ppl |
C |
T |
16: 5,104,901 |
R242H |
probably benign |
Het |
Ppp1r37 |
G |
T |
7: 19,532,111 |
Q577K |
probably benign |
Het |
Prcd |
A |
G |
11: 116,657,540 |
E25G |
probably damaging |
Het |
Prpsap2 |
C |
T |
11: 61,737,044 |
R202H |
probably damaging |
Het |
Ptgs1 |
A |
C |
2: 36,251,077 |
E512A |
probably damaging |
Het |
Radil |
T |
G |
5: 142,487,602 |
I535L |
probably benign |
Het |
Rbl2 |
G |
T |
8: 91,090,130 |
V373F |
probably benign |
Het |
Ryr1 |
T |
C |
7: 29,009,152 |
Y4802C |
probably benign |
Het |
Sdc2 |
A |
G |
15: 33,028,167 |
T144A |
probably benign |
Het |
Senp6 |
T |
C |
9: 80,114,116 |
|
probably null |
Het |
Sipa1l3 |
T |
C |
7: 29,397,206 |
D531G |
probably damaging |
Het |
Slc22a27 |
C |
A |
19: 7,910,046 |
C189F |
possibly damaging |
Het |
Srcin1 |
T |
C |
11: 97,533,497 |
|
probably null |
Het |
Svep1 |
C |
T |
4: 58,069,345 |
E2814K |
possibly damaging |
Het |
Tjp3 |
T |
G |
10: 81,277,912 |
H504P |
probably benign |
Het |
Tmprss4 |
T |
A |
9: 45,175,116 |
K378* |
probably null |
Het |
Tns4 |
C |
T |
11: 99,073,671 |
|
probably null |
Het |
Ttn |
T |
C |
2: 76,749,954 |
T15205A |
possibly damaging |
Het |
Ush2a |
G |
T |
1: 188,356,814 |
G322V |
probably benign |
Het |
Vac14 |
A |
T |
8: 110,636,472 |
|
probably null |
Het |
Vmn1r175 |
T |
G |
7: 23,808,947 |
D85A |
probably damaging |
Het |
Vmn2r93 |
T |
C |
17: 18,325,768 |
L634P |
probably damaging |
Het |
Zeb2 |
A |
T |
2: 45,111,259 |
|
probably benign |
Het |
Zfp616 |
T |
A |
11: 74,083,260 |
H118Q |
possibly damaging |
Het |
Zfp945 |
T |
A |
17: 22,850,981 |
H648L |
probably damaging |
Het |
Zscan29 |
G |
T |
2: 121,164,037 |
T489N |
probably damaging |
Het |
|