Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930407I10Rik |
T |
A |
15: 81,947,843 (GRCm39) |
I580N |
probably benign |
Het |
Adam9 |
C |
A |
8: 25,445,953 (GRCm39) |
V814F |
probably benign |
Het |
Aipl1 |
C |
T |
11: 71,928,253 (GRCm39) |
G11D |
probably damaging |
Het |
Akap9 |
C |
A |
5: 4,012,223 (GRCm39) |
Y975* |
probably null |
Het |
Akap9 |
C |
T |
5: 4,012,224 (GRCm39) |
Q976* |
probably null |
Het |
Bpnt1 |
T |
C |
1: 185,070,335 (GRCm39) |
M9T |
possibly damaging |
Het |
C4bp |
C |
A |
1: 130,584,912 (GRCm39) |
L41F |
probably damaging |
Het |
Car3 |
A |
T |
3: 14,929,450 (GRCm39) |
I59F |
|
Het |
Card11 |
T |
C |
5: 140,894,395 (GRCm39) |
D78G |
probably damaging |
Het |
Ccdc125 |
A |
G |
13: 100,820,876 (GRCm39) |
D199G |
possibly damaging |
Het |
Ccdc88c |
T |
C |
12: 100,911,749 (GRCm39) |
D695G |
possibly damaging |
Het |
Cd48 |
T |
A |
1: 171,532,432 (GRCm39) |
I237N |
possibly damaging |
Het |
Cep295 |
T |
C |
9: 15,244,499 (GRCm39) |
E1319G |
probably damaging |
Het |
Col6a4 |
C |
A |
9: 105,945,271 (GRCm39) |
A948S |
probably benign |
Het |
Dcp1b |
T |
A |
6: 119,196,993 (GRCm39) |
Y563* |
probably null |
Het |
Dcp2 |
C |
T |
18: 44,538,361 (GRCm39) |
R173C |
probably damaging |
Het |
Ddx59 |
T |
A |
1: 136,344,681 (GRCm39) |
Y117* |
probably null |
Het |
Dennd2a |
A |
T |
6: 39,485,294 (GRCm39) |
Y328* |
probably null |
Het |
Dhx30 |
A |
G |
9: 109,916,712 (GRCm39) |
L601P |
probably damaging |
Het |
Dip2c |
A |
G |
13: 9,709,431 (GRCm39) |
T1424A |
probably damaging |
Het |
Dlg2 |
A |
G |
7: 92,080,325 (GRCm39) |
N733S |
probably damaging |
Het |
Dnah5 |
C |
T |
15: 28,272,286 (GRCm39) |
T1030M |
probably benign |
Het |
Fgd5 |
A |
T |
6: 91,956,017 (GRCm39) |
R3* |
probably null |
Het |
Gbf1 |
A |
T |
19: 46,248,122 (GRCm39) |
T300S |
probably benign |
Het |
Gm5591 |
A |
T |
7: 38,219,721 (GRCm39) |
L384Q |
probably damaging |
Het |
Grm5 |
C |
T |
7: 87,765,484 (GRCm39) |
A904V |
probably benign |
Het |
Havcr1 |
T |
A |
11: 46,669,391 (GRCm39) |
V290E |
probably benign |
Het |
Hspb7 |
A |
G |
4: 141,149,241 (GRCm39) |
D49G |
possibly damaging |
Het |
Itpr2 |
A |
T |
6: 146,212,505 (GRCm39) |
I1537N |
probably damaging |
Het |
Kalrn |
T |
C |
16: 33,809,188 (GRCm39) |
T2567A |
probably benign |
Het |
Kat8 |
T |
C |
7: 127,524,100 (GRCm39) |
L380S |
probably benign |
Het |
Krt1c |
T |
A |
15: 101,719,792 (GRCm39) |
Y626F |
unknown |
Het |
Lrrk2 |
T |
A |
15: 91,636,388 (GRCm39) |
L1454* |
probably null |
Het |
Mgat4a |
C |
A |
1: 37,529,436 (GRCm39) |
V148F |
probably damaging |
Het |
Mtg1 |
T |
A |
7: 139,727,212 (GRCm39) |
Y238* |
probably null |
Het |
Neb |
T |
A |
2: 52,041,410 (GRCm39) |
Q6807L |
probably benign |
Het |
Nlrp9a |
C |
A |
7: 26,260,178 (GRCm39) |
F644L |
probably benign |
Het |
Pcdhb15 |
A |
G |
18: 37,607,263 (GRCm39) |
N165S |
|
Het |
Pcdhb5 |
C |
A |
18: 37,454,120 (GRCm39) |
Q167K |
probably damaging |
Het |
Per1 |
T |
A |
11: 68,998,855 (GRCm39) |
M1142K |
probably damaging |
Het |
Piezo1 |
A |
G |
8: 123,218,079 (GRCm39) |
V1220A |
|
Het |
Pkd1l1 |
T |
C |
11: 8,820,091 (GRCm39) |
T1713A |
|
Het |
Plec |
C |
A |
15: 76,115,377 (GRCm39) |
A66S |
probably benign |
Het |
Ppfia4 |
C |
A |
1: 134,247,044 (GRCm39) |
V559F |
possibly damaging |
Het |
Ppil6 |
T |
C |
10: 41,379,024 (GRCm39) |
S224P |
probably damaging |
Het |
Ppp2r2d |
T |
A |
7: 138,475,978 (GRCm39) |
M262K |
possibly damaging |
Het |
Prl7d1 |
A |
T |
13: 27,894,185 (GRCm39) |
M127K |
probably benign |
Het |
Rassf9 |
T |
A |
10: 102,381,577 (GRCm39) |
C320S |
probably benign |
Het |
Rbm19 |
AGAGGAGGAGGAGGAGGAGGA |
AGAGGAGGAGGAGGAGGA |
5: 120,278,345 (GRCm39) |
|
probably benign |
Het |
Rin3 |
T |
A |
12: 102,335,589 (GRCm39) |
L420* |
probably null |
Het |
Serpina3i |
A |
G |
12: 104,234,730 (GRCm39) |
T354A |
probably benign |
Het |
Serpinb9b |
A |
G |
13: 33,213,544 (GRCm39) |
S34G |
probably damaging |
Het |
Slc19a2 |
T |
C |
1: 164,076,895 (GRCm39) |
V25A |
probably damaging |
Het |
Slc1a2 |
G |
A |
2: 102,591,394 (GRCm39) |
E375K |
probably damaging |
Het |
Slfn9 |
T |
A |
11: 82,878,211 (GRCm39) |
Y306F |
possibly damaging |
Het |
Sparcl1 |
A |
T |
5: 104,241,030 (GRCm39) |
D131E |
possibly damaging |
Het |
Srl |
A |
T |
16: 4,301,031 (GRCm39) |
L680Q |
probably damaging |
Het |
Sufu |
G |
A |
19: 46,474,320 (GRCm39) |
W465* |
probably null |
Het |
Szt2 |
A |
G |
4: 118,248,151 (GRCm39) |
L691P |
probably damaging |
Het |
Tbc1d4 |
A |
T |
14: 101,703,096 (GRCm39) |
I783N |
probably damaging |
Het |
Tmem191 |
C |
T |
16: 17,094,526 (GRCm39) |
R62* |
probably null |
Het |
Tmem217 |
C |
A |
17: 29,745,690 (GRCm39) |
M13I |
possibly damaging |
Het |
Triobp |
T |
C |
15: 78,844,266 (GRCm39) |
S161P |
probably damaging |
Het |
Trp53bp2 |
T |
C |
1: 182,273,864 (GRCm39) |
V503A |
possibly damaging |
Het |
Tspoap1 |
G |
A |
11: 87,652,082 (GRCm39) |
|
probably benign |
Het |
Ttn |
T |
C |
2: 76,582,347 (GRCm39) |
T22849A |
probably damaging |
Het |
Ugt2b37 |
A |
T |
5: 87,402,217 (GRCm39) |
M138K |
probably damaging |
Het |
Uimc1 |
A |
T |
13: 55,223,646 (GRCm39) |
F209I |
possibly damaging |
Het |
Vipr1 |
G |
A |
9: 121,471,993 (GRCm39) |
|
probably null |
Het |
Wdr91 |
A |
T |
6: 34,861,302 (GRCm39) |
N633K |
possibly damaging |
Het |
Zfp618 |
T |
C |
4: 63,051,282 (GRCm39) |
S688P |
probably benign |
Het |
|
Other mutations in Ak2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02279:Ak2
|
APN |
4 |
128,893,030 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03068:Ak2
|
APN |
4 |
128,901,819 (GRCm39) |
splice site |
probably benign |
|
R0587:Ak2
|
UTSW |
4 |
128,896,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R1464:Ak2
|
UTSW |
4 |
128,896,152 (GRCm39) |
splice site |
probably benign |
|
R1727:Ak2
|
UTSW |
4 |
128,901,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R1878:Ak2
|
UTSW |
4 |
128,895,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R2002:Ak2
|
UTSW |
4 |
128,902,022 (GRCm39) |
missense |
probably benign |
0.00 |
R2030:Ak2
|
UTSW |
4 |
128,902,013 (GRCm39) |
missense |
probably benign |
0.00 |
R2061:Ak2
|
UTSW |
4 |
128,901,990 (GRCm39) |
missense |
probably damaging |
0.99 |
R4570:Ak2
|
UTSW |
4 |
128,895,960 (GRCm39) |
missense |
probably damaging |
0.99 |
R5108:Ak2
|
UTSW |
4 |
128,896,034 (GRCm39) |
missense |
probably damaging |
0.98 |
R5386:Ak2
|
UTSW |
4 |
128,901,965 (GRCm39) |
missense |
probably benign |
0.41 |
R5667:Ak2
|
UTSW |
4 |
128,902,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R5671:Ak2
|
UTSW |
4 |
128,902,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R6190:Ak2
|
UTSW |
4 |
128,892,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R6936:Ak2
|
UTSW |
4 |
128,893,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R7584:Ak2
|
UTSW |
4 |
128,893,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R9742:Ak2
|
UTSW |
4 |
128,901,961 (GRCm39) |
missense |
possibly damaging |
0.50 |
|