Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc2 |
G |
A |
19: 43,810,466 (GRCm39) |
R921H |
probably benign |
Het |
Adcy5 |
A |
G |
16: 35,119,859 (GRCm39) |
I1123V |
probably damaging |
Het |
Agr2 |
G |
C |
12: 36,045,565 (GRCm39) |
G17A |
probably benign |
Het |
Akap6 |
A |
T |
12: 53,188,831 (GRCm39) |
T2082S |
probably benign |
Het |
Asxl3 |
G |
T |
18: 22,657,401 (GRCm39) |
V1804F |
probably damaging |
Het |
Atat1 |
A |
G |
17: 36,220,381 (GRCm39) |
V37A |
probably benign |
Het |
Atp1a3 |
A |
T |
7: 24,689,212 (GRCm39) |
|
probably null |
Het |
Bpifb1 |
A |
G |
2: 154,051,848 (GRCm39) |
T218A |
probably benign |
Het |
C030006K11Rik |
T |
A |
15: 76,607,961 (GRCm39) |
Q19L |
probably benign |
Het |
Ccdc138 |
T |
C |
10: 58,380,893 (GRCm39) |
F508S |
probably damaging |
Het |
Ccdc81 |
T |
A |
7: 89,542,358 (GRCm39) |
M173L |
probably benign |
Het |
Cdhr1 |
T |
C |
14: 36,815,976 (GRCm39) |
I141V |
probably benign |
Het |
Chia1 |
T |
C |
3: 106,035,777 (GRCm39) |
F206L |
probably benign |
Het |
Clca3a2 |
C |
T |
3: 144,511,475 (GRCm39) |
G640E |
probably damaging |
Het |
Clcn7 |
T |
C |
17: 25,376,497 (GRCm39) |
V609A |
probably damaging |
Het |
Cmklr2 |
T |
C |
1: 63,223,145 (GRCm39) |
E30G |
probably benign |
Het |
Col22a1 |
C |
A |
15: 71,753,523 (GRCm39) |
G126* |
probably null |
Het |
Cpne7 |
C |
T |
8: 123,856,951 (GRCm39) |
P402L |
probably damaging |
Het |
Ctcfl |
A |
T |
2: 172,959,044 (GRCm39) |
D227E |
probably benign |
Het |
Cwf19l2 |
A |
G |
9: 3,417,942 (GRCm39) |
D134G |
probably benign |
Het |
Cyp2c65 |
C |
A |
19: 39,061,663 (GRCm39) |
C216* |
probably null |
Het |
Cyp2d12 |
T |
A |
15: 82,443,423 (GRCm39) |
C462S |
probably null |
Het |
Cyp4a12a |
A |
C |
4: 115,189,199 (GRCm39) |
*509Y |
probably null |
Het |
Cyp4a12b |
A |
G |
4: 115,290,865 (GRCm39) |
M298V |
probably benign |
Het |
Dennd4b |
T |
C |
3: 90,178,188 (GRCm39) |
V471A |
probably benign |
Het |
Dlc1 |
A |
G |
8: 37,405,055 (GRCm39) |
S245P |
possibly damaging |
Het |
Dnah1 |
C |
T |
14: 31,001,128 (GRCm39) |
G2406S |
probably benign |
Het |
Dnah8 |
A |
G |
17: 30,956,401 (GRCm39) |
K2127R |
probably damaging |
Het |
Dusp13b |
G |
A |
14: 21,790,233 (GRCm39) |
R38C |
probably benign |
Het |
Ebf2 |
T |
A |
14: 67,472,594 (GRCm39) |
I4N |
probably benign |
Het |
Eef1ece2 |
C |
T |
16: 20,459,375 (GRCm39) |
P570L |
probably damaging |
Het |
Fcgbp |
A |
G |
7: 27,790,908 (GRCm39) |
N723S |
possibly damaging |
Het |
Galnt15 |
T |
A |
14: 31,770,027 (GRCm39) |
V368E |
probably damaging |
Het |
Garem2 |
A |
G |
5: 30,313,262 (GRCm39) |
E42G |
possibly damaging |
Het |
Gcc1 |
C |
T |
6: 28,418,182 (GRCm39) |
S717N |
probably damaging |
Het |
Gfm2 |
T |
C |
13: 97,309,201 (GRCm39) |
|
probably null |
Het |
Helb |
T |
C |
10: 119,920,790 (GRCm39) |
D1051G |
possibly damaging |
Het |
Helz2 |
T |
A |
2: 180,874,261 (GRCm39) |
I2078F |
possibly damaging |
Het |
Hsph1 |
A |
T |
5: 149,553,270 (GRCm39) |
V297D |
probably damaging |
Het |
Ifnar1 |
A |
G |
16: 91,302,079 (GRCm39) |
Y518C |
probably benign |
Het |
Kcnip2 |
T |
A |
19: 45,783,210 (GRCm39) |
D153V |
probably damaging |
Het |
Kif15 |
A |
T |
9: 122,846,492 (GRCm39) |
|
probably benign |
Het |
Kif21b |
T |
C |
1: 136,073,042 (GRCm39) |
F147L |
probably damaging |
Het |
Klhl29 |
T |
C |
12: 5,140,537 (GRCm39) |
R702G |
probably damaging |
Het |
Lemd3 |
C |
T |
10: 120,767,878 (GRCm39) |
E667K |
possibly damaging |
Het |
Loxl3 |
T |
C |
6: 83,012,503 (GRCm39) |
L14P |
probably damaging |
Het |
Lrrd1 |
A |
T |
5: 3,900,963 (GRCm39) |
K423* |
probably null |
Het |
Mia2 |
A |
G |
12: 59,155,586 (GRCm39) |
D433G |
probably damaging |
Het |
Mpp2 |
G |
T |
11: 101,954,099 (GRCm39) |
A216E |
probably benign |
Het |
Mro |
T |
C |
18: 74,009,911 (GRCm39) |
|
probably null |
Het |
Mybpc1 |
T |
G |
10: 88,358,906 (GRCm39) |
Y1081S |
probably damaging |
Het |
Myh8 |
T |
G |
11: 67,190,141 (GRCm39) |
S1260R |
possibly damaging |
Het |
Myo3b |
T |
C |
2: 70,082,094 (GRCm39) |
V618A |
probably damaging |
Het |
Naip2 |
T |
G |
13: 100,314,776 (GRCm39) |
D334A |
possibly damaging |
Het |
Naip5 |
T |
A |
13: 100,356,338 (GRCm39) |
E1092D |
probably benign |
Het |
Nlrp4c |
T |
C |
7: 6,107,608 (GRCm39) |
*983Q |
probably null |
Het |
Nlrp9a |
T |
G |
7: 26,257,698 (GRCm39) |
F439V |
probably damaging |
Het |
Nploc4 |
A |
T |
11: 120,319,368 (GRCm39) |
L64H |
probably damaging |
Het |
Otof |
G |
A |
5: 30,537,532 (GRCm39) |
S1259F |
probably benign |
Het |
Pde4dip |
T |
C |
3: 97,599,675 (GRCm39) |
T2438A |
probably damaging |
Het |
Pex1 |
A |
G |
5: 3,686,844 (GRCm39) |
T1242A |
probably damaging |
Het |
Pink1 |
A |
T |
4: 138,043,056 (GRCm39) |
|
probably benign |
Het |
Prkcq |
A |
G |
2: 11,251,819 (GRCm39) |
T219A |
probably damaging |
Het |
Ptcd3 |
A |
T |
6: 71,880,458 (GRCm39) |
Y88* |
probably null |
Het |
Ptpru |
A |
G |
4: 131,515,691 (GRCm39) |
Y888H |
probably damaging |
Het |
Rapgef6 |
A |
G |
11: 54,578,667 (GRCm39) |
N1063S |
probably benign |
Het |
Slc1a4 |
G |
A |
11: 20,282,532 (GRCm39) |
|
probably benign |
Het |
Slc4a4 |
T |
C |
5: 89,205,568 (GRCm39) |
|
probably benign |
Het |
Slc6a18 |
A |
T |
13: 73,819,822 (GRCm39) |
N249K |
possibly damaging |
Het |
Slco2b1 |
T |
G |
7: 99,338,214 (GRCm39) |
I104L |
probably damaging |
Het |
Syne3 |
A |
T |
12: 104,905,871 (GRCm39) |
S897R |
probably benign |
Het |
Tlcd5 |
C |
T |
9: 43,022,664 (GRCm39) |
R230Q |
probably benign |
Het |
Tnni3k |
A |
G |
3: 154,744,146 (GRCm39) |
S69P |
probably damaging |
Het |
Tnpo2 |
A |
G |
8: 85,780,163 (GRCm39) |
K700E |
probably benign |
Het |
Top3a |
T |
C |
11: 60,636,695 (GRCm39) |
K657E |
probably damaging |
Het |
Trgv4 |
C |
T |
13: 19,369,169 (GRCm39) |
Q7* |
probably null |
Het |
Trim6 |
T |
C |
7: 103,875,159 (GRCm39) |
L132P |
probably damaging |
Het |
Tshz1 |
T |
C |
18: 84,032,987 (GRCm39) |
T474A |
probably benign |
Het |
Unc13d |
AATGCCTCCCATGCC |
AATGCCTCCCATGCCTCCCATGCC |
11: 115,958,998 (GRCm39) |
|
probably benign |
Het |
Vmn1r179 |
A |
T |
7: 23,628,234 (GRCm39) |
I142L |
probably benign |
Het |
Zbtb2 |
A |
T |
10: 4,319,183 (GRCm39) |
F281Y |
probably damaging |
Het |
Zfp318 |
T |
C |
17: 46,723,433 (GRCm39) |
V1812A |
probably benign |
Het |
|
Other mutations in Ola1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00864:Ola1
|
APN |
2 |
72,987,241 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01969:Ola1
|
APN |
2 |
72,930,490 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02605:Ola1
|
APN |
2 |
72,972,644 (GRCm39) |
splice site |
probably benign |
|
IGL02987:Ola1
|
APN |
2 |
72,987,242 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03171:Ola1
|
APN |
2 |
72,987,197 (GRCm39) |
missense |
probably benign |
0.24 |
R0602:Ola1
|
UTSW |
2 |
72,924,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R1167:Ola1
|
UTSW |
2 |
72,927,538 (GRCm39) |
missense |
probably damaging |
0.99 |
R1474:Ola1
|
UTSW |
2 |
72,987,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R1650:Ola1
|
UTSW |
2 |
72,987,238 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1781:Ola1
|
UTSW |
2 |
72,987,099 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3732:Ola1
|
UTSW |
2 |
72,987,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R3732:Ola1
|
UTSW |
2 |
72,987,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R3733:Ola1
|
UTSW |
2 |
72,987,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R3918:Ola1
|
UTSW |
2 |
72,972,683 (GRCm39) |
missense |
probably benign |
0.33 |
R4650:Ola1
|
UTSW |
2 |
72,972,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R5304:Ola1
|
UTSW |
2 |
73,029,778 (GRCm39) |
missense |
probably damaging |
0.99 |
R5352:Ola1
|
UTSW |
2 |
72,929,674 (GRCm39) |
missense |
probably damaging |
0.99 |
R5918:Ola1
|
UTSW |
2 |
72,987,128 (GRCm39) |
missense |
probably benign |
0.18 |
R6062:Ola1
|
UTSW |
2 |
73,029,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R6858:Ola1
|
UTSW |
2 |
72,927,574 (GRCm39) |
missense |
probably damaging |
0.97 |
R7077:Ola1
|
UTSW |
2 |
72,972,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R8223:Ola1
|
UTSW |
2 |
72,929,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R8343:Ola1
|
UTSW |
2 |
73,029,745 (GRCm39) |
missense |
probably damaging |
0.99 |
R9258:Ola1
|
UTSW |
2 |
72,929,732 (GRCm39) |
missense |
probably damaging |
0.96 |
R9641:Ola1
|
UTSW |
2 |
73,033,784 (GRCm39) |
missense |
probably benign |
0.02 |
|