Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acad10 |
T |
C |
5: 121,784,929 (GRCm39) |
|
probably null |
Het |
Adamtsl3 |
T |
G |
7: 82,255,728 (GRCm39) |
M1580R |
possibly damaging |
Het |
Alg9 |
T |
C |
9: 50,687,942 (GRCm39) |
I78T |
probably damaging |
Het |
Ankmy2 |
G |
T |
12: 36,207,143 (GRCm39) |
|
probably benign |
Het |
Ankrd11 |
G |
T |
8: 123,621,498 (GRCm39) |
L785M |
probably damaging |
Het |
Atrnl1 |
T |
A |
19: 57,684,763 (GRCm39) |
D796E |
probably benign |
Het |
C1s2 |
A |
G |
6: 124,607,017 (GRCm39) |
V277A |
possibly damaging |
Het |
Ccdc121rt3 |
A |
G |
5: 112,503,383 (GRCm39) |
I107T |
probably benign |
Het |
Cldn15 |
A |
G |
5: 136,997,015 (GRCm39) |
M19V |
probably benign |
Het |
Cldn23 |
T |
G |
8: 36,293,417 (GRCm39) |
S24R |
possibly damaging |
Het |
Cnr1 |
T |
A |
4: 33,944,416 (GRCm39) |
I268N |
probably damaging |
Het |
Csf2ra |
A |
T |
19: 61,215,024 (GRCm39) |
W147R |
probably damaging |
Het |
Ctsb |
G |
T |
14: 63,370,765 (GRCm39) |
|
probably benign |
Het |
D430041D05Rik |
A |
G |
2: 104,088,874 (GRCm39) |
M34T |
probably benign |
Het |
Dmtf1 |
T |
C |
5: 9,176,564 (GRCm39) |
I463V |
probably damaging |
Het |
Dnah7a |
T |
A |
1: 53,670,842 (GRCm39) |
D470V |
probably benign |
Het |
Dtx4 |
A |
G |
19: 12,459,500 (GRCm39) |
S435P |
probably benign |
Het |
Ear2 |
T |
A |
14: 44,340,495 (GRCm39) |
M51K |
probably damaging |
Het |
Efcab3 |
T |
A |
11: 104,615,366 (GRCm39) |
L711* |
probably null |
Het |
Elmo1 |
T |
A |
13: 20,464,973 (GRCm39) |
|
probably null |
Het |
Faf1 |
T |
A |
4: 109,593,794 (GRCm39) |
I124N |
probably damaging |
Het |
Gkap1 |
A |
C |
13: 58,384,799 (GRCm39) |
|
probably null |
Het |
Glipr2 |
T |
C |
4: 43,957,770 (GRCm39) |
S4P |
probably benign |
Het |
Gm38119 |
A |
T |
3: 92,645,337 (GRCm39) |
C86S |
unknown |
Het |
Gpr171 |
T |
G |
3: 59,005,320 (GRCm39) |
I152L |
probably benign |
Het |
Hes7 |
T |
A |
11: 69,012,352 (GRCm39) |
T9S |
unknown |
Het |
Homer3 |
T |
C |
8: 70,743,662 (GRCm39) |
V180A |
probably benign |
Het |
Irx1 |
T |
A |
13: 72,108,176 (GRCm39) |
M169L |
probably benign |
Het |
Kap |
A |
G |
6: 133,828,690 (GRCm39) |
|
probably null |
Het |
Mgat5b |
A |
G |
11: 116,857,627 (GRCm39) |
M2V |
|
Het |
Mob4 |
C |
T |
1: 55,187,479 (GRCm39) |
Q76* |
probably null |
Het |
Or10w3 |
T |
A |
19: 13,704,207 (GRCm39) |
I194N |
possibly damaging |
Het |
Or8b47 |
A |
T |
9: 38,435,013 (GRCm39) |
|
probably null |
Het |
Or8g26 |
A |
G |
9: 39,096,056 (GRCm39) |
D191G |
probably benign |
Het |
Pate14 |
C |
T |
9: 36,549,159 (GRCm39) |
G34R |
possibly damaging |
Het |
Pcdha9 |
A |
T |
18: 37,132,689 (GRCm39) |
Q586L |
probably benign |
Het |
Pgk2 |
T |
A |
17: 40,518,409 (GRCm39) |
I340F |
probably benign |
Het |
Prex1 |
G |
A |
2: 166,419,810 (GRCm39) |
Q1289* |
probably null |
Het |
Prr22 |
A |
G |
17: 57,078,819 (GRCm39) |
D324G |
possibly damaging |
Het |
Rab2b |
A |
T |
14: 52,501,217 (GRCm39) |
S201T |
probably benign |
Het |
Rdh1 |
T |
A |
10: 127,596,121 (GRCm39) |
|
probably null |
Het |
Rhbdl1 |
G |
T |
17: 26,055,123 (GRCm39) |
N82K |
probably benign |
Het |
Rspo1 |
C |
A |
4: 124,885,210 (GRCm39) |
Q29K |
possibly damaging |
Het |
Rtp3 |
A |
T |
9: 110,814,948 (GRCm39) |
Y472* |
probably null |
Het |
Senp5 |
T |
A |
16: 31,809,252 (GRCm39) |
M1L |
unknown |
Het |
Slfn4 |
A |
T |
11: 83,078,389 (GRCm39) |
|
probably null |
Het |
Stab1 |
A |
G |
14: 30,863,413 (GRCm39) |
V2091A |
possibly damaging |
Het |
Tpr |
A |
G |
1: 150,320,180 (GRCm39) |
T2243A |
probably benign |
Het |
Tubgcp6 |
A |
T |
15: 88,985,604 (GRCm39) |
N1544K |
probably damaging |
Het |
Uqcc1 |
T |
C |
2: 155,700,066 (GRCm39) |
N202S |
probably benign |
Het |
Vmn2r18 |
C |
T |
5: 151,510,158 (GRCm39) |
E72K |
possibly damaging |
Het |
Zfp654 |
C |
A |
16: 64,606,570 (GRCm39) |
C3F |
probably damaging |
Het |
Zfp804b |
T |
C |
5: 6,821,263 (GRCm39) |
E600G |
possibly damaging |
Het |
|
Other mutations in Stk32c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02003:Stk32c
|
APN |
7 |
138,768,069 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL02559:Stk32c
|
APN |
7 |
138,700,606 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02805:Stk32c
|
APN |
7 |
138,701,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R0531:Stk32c
|
UTSW |
7 |
138,700,636 (GRCm39) |
missense |
probably damaging |
0.97 |
R0622:Stk32c
|
UTSW |
7 |
138,768,026 (GRCm39) |
missense |
probably benign |
0.00 |
R1140:Stk32c
|
UTSW |
7 |
138,705,095 (GRCm39) |
missense |
probably damaging |
0.99 |
R1473:Stk32c
|
UTSW |
7 |
138,705,095 (GRCm39) |
missense |
probably damaging |
0.99 |
R1589:Stk32c
|
UTSW |
7 |
138,698,931 (GRCm39) |
critical splice donor site |
probably null |
|
R1697:Stk32c
|
UTSW |
7 |
138,701,740 (GRCm39) |
missense |
probably benign |
0.25 |
R1855:Stk32c
|
UTSW |
7 |
138,701,363 (GRCm39) |
missense |
probably damaging |
0.97 |
R4290:Stk32c
|
UTSW |
7 |
138,700,704 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4293:Stk32c
|
UTSW |
7 |
138,700,704 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4295:Stk32c
|
UTSW |
7 |
138,700,704 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5323:Stk32c
|
UTSW |
7 |
138,699,276 (GRCm39) |
missense |
probably benign |
0.07 |
R5854:Stk32c
|
UTSW |
7 |
138,768,195 (GRCm39) |
intron |
probably benign |
|
R5907:Stk32c
|
UTSW |
7 |
138,700,590 (GRCm39) |
missense |
probably benign |
0.32 |
R6115:Stk32c
|
UTSW |
7 |
138,700,628 (GRCm39) |
nonsense |
probably null |
|
R6117:Stk32c
|
UTSW |
7 |
138,702,839 (GRCm39) |
nonsense |
probably null |
|
R6176:Stk32c
|
UTSW |
7 |
138,700,691 (GRCm39) |
missense |
probably benign |
0.02 |
R6460:Stk32c
|
UTSW |
7 |
138,685,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R6695:Stk32c
|
UTSW |
7 |
138,702,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R6745:Stk32c
|
UTSW |
7 |
138,702,809 (GRCm39) |
missense |
probably damaging |
0.99 |
R7177:Stk32c
|
UTSW |
7 |
138,684,218 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7676:Stk32c
|
UTSW |
7 |
138,685,220 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8977:Stk32c
|
UTSW |
7 |
138,705,161 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9004:Stk32c
|
UTSW |
7 |
138,702,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R9117:Stk32c
|
UTSW |
7 |
138,768,141 (GRCm39) |
missense |
unknown |
|
R9481:Stk32c
|
UTSW |
7 |
138,768,173 (GRCm39) |
missense |
unknown |
|
|