Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aatk |
A |
G |
11: 119,912,277 (GRCm39) |
I56T |
probably benign |
Het |
Adissp |
T |
C |
2: 130,993,682 (GRCm39) |
|
probably null |
Het |
Akr1c12 |
A |
G |
13: 4,325,796 (GRCm39) |
L99S |
probably damaging |
Het |
Azin1 |
C |
A |
15: 38,493,871 (GRCm39) |
V251F |
possibly damaging |
Het |
C2cd3 |
A |
T |
7: 100,065,262 (GRCm39) |
M305L |
|
Het |
Casz1 |
A |
G |
4: 149,023,320 (GRCm39) |
T742A |
probably damaging |
Het |
Cbfa2t2 |
A |
G |
2: 154,352,426 (GRCm39) |
|
probably null |
Het |
Clec2e |
T |
A |
6: 129,071,420 (GRCm39) |
Y139F |
possibly damaging |
Het |
Crisp2 |
T |
A |
17: 41,094,724 (GRCm39) |
N117I |
possibly damaging |
Het |
Ddx52 |
A |
T |
11: 83,833,008 (GRCm39) |
D2V |
probably damaging |
Het |
Dmpk |
T |
A |
7: 18,824,946 (GRCm39) |
V442E |
probably benign |
Het |
Dnah2 |
A |
T |
11: 69,368,942 (GRCm39) |
M1654K |
probably benign |
Het |
Eln |
AGGGACACCAGCACCAGCCCCAAATCCGGGGACACCAGCACCAGCCCCAAATCCGGGGACACCAGCACCAGCCCCAAATCCGGGGACACCAGCACCAGCCCCAAATCCAGGGACACCAGC |
AGGGACACCAGCACCAGCCCCAAATCCGGGGACACCAGCACCAGCCCCAAATCCGGGGACACCAGCACCAGCCCCAAATCCAGGGACACCAGC |
5: 134,739,935 (GRCm39) |
|
probably benign |
Het |
Erlec1 |
A |
G |
11: 30,885,054 (GRCm39) |
V411A |
probably damaging |
Het |
Fktn |
G |
A |
4: 53,734,854 (GRCm39) |
G125D |
probably benign |
Het |
Fry |
A |
G |
5: 150,356,994 (GRCm39) |
E1847G |
possibly damaging |
Het |
Gck |
A |
G |
11: 5,899,553 (GRCm39) |
|
probably null |
Het |
Gga2 |
T |
C |
7: 121,603,195 (GRCm39) |
D167G |
probably damaging |
Het |
Gprc6a |
A |
G |
10: 51,491,506 (GRCm39) |
S748P |
probably damaging |
Het |
H2-M10.2 |
T |
C |
17: 36,595,643 (GRCm39) |
R216G |
probably benign |
Het |
H2-M2 |
T |
A |
17: 37,792,215 (GRCm39) |
I312F |
probably benign |
Het |
Havcr2 |
A |
T |
11: 46,347,350 (GRCm39) |
Y109F |
probably damaging |
Het |
Hoga1 |
T |
C |
19: 42,048,333 (GRCm39) |
V67A |
|
Het |
Ift70b |
T |
A |
2: 75,768,391 (GRCm39) |
I121F |
possibly damaging |
Het |
Kcnk12 |
C |
A |
17: 88,104,507 (GRCm39) |
V126L |
possibly damaging |
Het |
Klc1 |
A |
G |
12: 111,738,950 (GRCm39) |
E66G |
probably damaging |
Het |
Klhl2 |
A |
T |
8: 65,205,870 (GRCm39) |
Y350* |
probably null |
Het |
Letm1 |
T |
C |
5: 33,926,802 (GRCm39) |
H165R |
probably damaging |
Het |
Luc7l2 |
T |
C |
6: 38,547,489 (GRCm39) |
C36R |
probably damaging |
Het |
Mab21l1 |
A |
G |
3: 55,690,674 (GRCm39) |
N87S |
probably damaging |
Het |
Mdn1 |
A |
G |
4: 32,678,414 (GRCm39) |
T681A |
probably damaging |
Het |
Mrc1 |
C |
T |
2: 14,312,790 (GRCm39) |
T904I |
possibly damaging |
Het |
Mrpl38 |
A |
G |
11: 116,023,276 (GRCm39) |
S326P |
probably damaging |
Het |
Mtr |
T |
G |
13: 12,268,764 (GRCm39) |
K32N |
probably benign |
Het |
Mybpc3 |
T |
A |
2: 90,965,478 (GRCm39) |
C1128* |
probably null |
Het |
Ncdn |
T |
C |
4: 126,645,762 (GRCm39) |
D49G |
probably damaging |
Het |
Nfkbiz |
G |
A |
16: 55,642,337 (GRCm39) |
T27I |
probably damaging |
Het |
Npnt |
A |
T |
3: 132,653,866 (GRCm39) |
Y38* |
probably null |
Het |
Nrxn2 |
A |
G |
19: 6,581,931 (GRCm39) |
E1622G |
probably benign |
Het |
Nutm2 |
T |
C |
13: 50,626,964 (GRCm39) |
I373T |
probably damaging |
Het |
Or4c58 |
T |
C |
2: 89,674,715 (GRCm39) |
I201V |
probably benign |
Het |
Or51m1 |
T |
C |
7: 103,578,980 (GRCm39) |
S317P |
possibly damaging |
Het |
Osbp2 |
A |
G |
11: 3,662,170 (GRCm39) |
S228P |
probably damaging |
Het |
Pbx3 |
C |
T |
2: 34,103,348 (GRCm39) |
R208Q |
probably damaging |
Het |
Pcdhgb5 |
T |
C |
18: 37,864,838 (GRCm39) |
V211A |
probably benign |
Het |
Pi16 |
C |
T |
17: 29,544,899 (GRCm39) |
T151M |
probably damaging |
Het |
Pramel39-ps |
G |
T |
5: 94,451,001 (GRCm39) |
P375H |
probably damaging |
Het |
Ptpro |
T |
C |
6: 137,420,933 (GRCm39) |
I1068T |
probably benign |
Het |
Rbl1 |
A |
T |
2: 157,035,154 (GRCm39) |
Y309N |
probably damaging |
Het |
Rsf1 |
GGCGGCGGC |
GGCGGCGGCCGCGGCGGC |
7: 97,229,134 (GRCm39) |
|
probably benign |
Het |
Serpina3g |
G |
C |
12: 104,206,518 (GRCm39) |
E106D |
probably benign |
Het |
Slc4a11 |
C |
T |
2: 130,533,664 (GRCm39) |
A100T |
probably damaging |
Het |
Son |
G |
C |
16: 91,454,508 (GRCm39) |
R1085P |
probably damaging |
Het |
Tasor |
A |
T |
14: 27,163,927 (GRCm39) |
I238F |
probably damaging |
Het |
Tbx18 |
C |
A |
9: 87,612,675 (GRCm39) |
A75S |
probably benign |
Het |
Tmem232 |
C |
A |
17: 65,792,881 (GRCm39) |
Q105H |
probably damaging |
Het |
Ttc29 |
A |
G |
8: 79,060,390 (GRCm39) |
I437V |
probably benign |
Het |
Ttn |
T |
A |
2: 76,621,887 (GRCm39) |
I15552L |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,750,313 (GRCm39) |
T3579S |
probably benign |
Het |
Vps11 |
A |
G |
9: 44,267,719 (GRCm39) |
F298L |
probably benign |
Het |
Wbp11 |
T |
C |
6: 136,791,259 (GRCm39) |
T625A |
unknown |
Het |
Xylb |
T |
A |
9: 119,215,428 (GRCm39) |
N460K |
probably damaging |
Het |
Znrf4 |
C |
A |
17: 56,819,218 (GRCm39) |
V30F |
probably damaging |
Het |
|
Other mutations in Btbd16 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00885:Btbd16
|
APN |
7 |
130,390,552 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01020:Btbd16
|
APN |
7 |
130,426,091 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01098:Btbd16
|
APN |
7 |
130,424,975 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01412:Btbd16
|
APN |
7 |
130,407,549 (GRCm39) |
critical splice acceptor site |
probably null |
|
1mM(1):Btbd16
|
UTSW |
7 |
130,423,221 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0063:Btbd16
|
UTSW |
7 |
130,424,896 (GRCm39) |
missense |
probably benign |
0.25 |
R0063:Btbd16
|
UTSW |
7 |
130,424,896 (GRCm39) |
missense |
probably benign |
0.25 |
R0147:Btbd16
|
UTSW |
7 |
130,381,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R0436:Btbd16
|
UTSW |
7 |
130,387,783 (GRCm39) |
missense |
probably benign |
0.10 |
R0715:Btbd16
|
UTSW |
7 |
130,390,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R2127:Btbd16
|
UTSW |
7 |
130,386,038 (GRCm39) |
missense |
probably benign |
0.17 |
R2411:Btbd16
|
UTSW |
7 |
130,391,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R3798:Btbd16
|
UTSW |
7 |
130,378,870 (GRCm39) |
missense |
probably benign |
0.43 |
R5595:Btbd16
|
UTSW |
7 |
130,425,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R5595:Btbd16
|
UTSW |
7 |
130,425,033 (GRCm39) |
missense |
possibly damaging |
0.52 |
R5839:Btbd16
|
UTSW |
7 |
130,417,538 (GRCm39) |
critical splice donor site |
probably null |
|
R5933:Btbd16
|
UTSW |
7 |
130,386,011 (GRCm39) |
missense |
probably damaging |
0.99 |
R6029:Btbd16
|
UTSW |
7 |
130,420,802 (GRCm39) |
missense |
probably benign |
0.17 |
R7255:Btbd16
|
UTSW |
7 |
130,387,722 (GRCm39) |
missense |
probably benign |
0.04 |
R7355:Btbd16
|
UTSW |
7 |
130,423,173 (GRCm39) |
missense |
probably benign |
0.01 |
R7405:Btbd16
|
UTSW |
7 |
130,407,586 (GRCm39) |
missense |
probably benign |
0.08 |
R7527:Btbd16
|
UTSW |
7 |
130,422,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R7980:Btbd16
|
UTSW |
7 |
130,426,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R8151:Btbd16
|
UTSW |
7 |
130,398,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R8429:Btbd16
|
UTSW |
7 |
130,397,067 (GRCm39) |
missense |
probably benign |
|
R9142:Btbd16
|
UTSW |
7 |
130,417,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R9143:Btbd16
|
UTSW |
7 |
130,417,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R9161:Btbd16
|
UTSW |
7 |
130,417,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R9214:Btbd16
|
UTSW |
7 |
130,381,437 (GRCm39) |
critical splice donor site |
probably null |
|
R9266:Btbd16
|
UTSW |
7 |
130,417,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R9267:Btbd16
|
UTSW |
7 |
130,417,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R9269:Btbd16
|
UTSW |
7 |
130,417,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R9360:Btbd16
|
UTSW |
7 |
130,417,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R9362:Btbd16
|
UTSW |
7 |
130,417,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R9392:Btbd16
|
UTSW |
7 |
130,417,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R9418:Btbd16
|
UTSW |
7 |
130,417,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R9431:Btbd16
|
UTSW |
7 |
130,417,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R9610:Btbd16
|
UTSW |
7 |
130,407,595 (GRCm39) |
missense |
probably benign |
0.05 |
R9611:Btbd16
|
UTSW |
7 |
130,407,595 (GRCm39) |
missense |
probably benign |
0.05 |
X0064:Btbd16
|
UTSW |
7 |
130,424,900 (GRCm39) |
missense |
probably damaging |
1.00 |
|