Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930407I10Rik |
G |
T |
15: 81,949,301 (GRCm39) |
R1066L |
probably benign |
Het |
Abca14 |
A |
C |
7: 119,893,425 (GRCm39) |
I1292L |
probably benign |
Het |
Adam34l |
T |
A |
8: 44,079,538 (GRCm39) |
T229S |
probably benign |
Het |
Adamtsl1 |
T |
G |
4: 86,261,382 (GRCm39) |
F1206V |
probably benign |
Het |
Agl |
T |
C |
3: 116,582,293 (GRCm39) |
H243R |
probably damaging |
Het |
Btn2a2 |
A |
C |
13: 23,666,040 (GRCm39) |
L264R |
probably damaging |
Het |
Ccdc33 |
A |
T |
9: 57,939,995 (GRCm39) |
S749T |
probably benign |
Het |
Cd55b |
CTTTT |
CTTTTT |
1: 130,347,337 (GRCm39) |
|
probably null |
Het |
Cdh8 |
A |
G |
8: 99,757,498 (GRCm39) |
I700T |
possibly damaging |
Het |
Cfap65 |
A |
G |
1: 74,949,902 (GRCm39) |
L1201P |
probably damaging |
Het |
Chsy3 |
C |
T |
18: 59,308,941 (GRCm39) |
Q65* |
probably null |
Het |
Clic5 |
T |
A |
17: 44,586,228 (GRCm39) |
L239* |
probably null |
Het |
Corin |
T |
C |
5: 72,462,361 (GRCm39) |
D957G |
probably damaging |
Het |
Cped1 |
A |
T |
6: 22,132,277 (GRCm39) |
Y486F |
probably damaging |
Het |
Csnk1g3 |
C |
T |
18: 54,081,151 (GRCm39) |
T374M |
probably benign |
Het |
D930020B18Rik |
T |
A |
10: 121,503,429 (GRCm39) |
C201* |
probably null |
Het |
Dnah2 |
A |
G |
11: 69,326,193 (GRCm39) |
F3653L |
probably damaging |
Het |
F11r |
GGTGTG |
GGTGTGTG |
1: 171,290,656 (GRCm39) |
|
probably null |
Het |
Foxj3 |
T |
G |
4: 119,478,808 (GRCm39) |
S455R |
unknown |
Het |
Gcnt3 |
T |
C |
9: 69,941,455 (GRCm39) |
D371G |
probably damaging |
Het |
Gm10837 |
A |
G |
14: 122,728,193 (GRCm39) |
E23G |
unknown |
Het |
Hivep3 |
T |
C |
4: 119,980,098 (GRCm39) |
V1712A |
probably damaging |
Het |
Hjurp |
GT |
GTT |
1: 88,194,246 (GRCm39) |
|
probably null |
Het |
Hoxa2 |
A |
G |
6: 52,140,041 (GRCm39) |
V315A |
probably damaging |
Het |
Irx5 |
A |
T |
8: 93,086,241 (GRCm39) |
Y108F |
possibly damaging |
Het |
Itsn1 |
T |
C |
16: 91,608,996 (GRCm39) |
I248T |
probably damaging |
Het |
Kcnb1 |
T |
C |
2: 166,946,361 (GRCm39) |
K829R |
probably benign |
Het |
Klhl17 |
A |
G |
4: 156,314,510 (GRCm39) |
V635A |
unknown |
Het |
Krr1 |
C |
T |
10: 111,815,834 (GRCm39) |
R234* |
probably null |
Het |
Lrrc7 |
A |
T |
3: 157,915,387 (GRCm39) |
D209E |
probably benign |
Het |
Mcm2 |
T |
C |
6: 88,874,293 (GRCm39) |
E71G |
probably damaging |
Het |
Mroh5 |
C |
A |
15: 73,691,139 (GRCm39) |
K10N |
probably damaging |
Het |
Myh3 |
A |
G |
11: 66,992,005 (GRCm39) |
E1850G |
probably damaging |
Het |
Nedd9 |
T |
C |
13: 41,492,319 (GRCm39) |
I64V |
probably benign |
Het |
Nisch |
A |
G |
14: 30,908,658 (GRCm39) |
S456P |
possibly damaging |
Het |
Nrcam |
T |
C |
12: 44,610,896 (GRCm39) |
V532A |
probably benign |
Het |
Or51k1 |
T |
C |
7: 103,661,330 (GRCm39) |
D193G |
possibly damaging |
Het |
Or5p51 |
T |
G |
7: 107,444,124 (GRCm39) |
D272A |
probably damaging |
Het |
Or7g32 |
T |
C |
9: 19,408,796 (GRCm39) |
F251L |
probably damaging |
Het |
Or8k17 |
C |
T |
2: 86,066,862 (GRCm39) |
V106M |
probably benign |
Het |
Plekhg1 |
C |
T |
10: 3,907,521 (GRCm39) |
P868S |
|
Het |
Ptf1a |
A |
G |
2: 19,450,760 (GRCm39) |
Q30R |
possibly damaging |
Het |
Ptgs1 |
G |
T |
2: 36,141,179 (GRCm39) |
C542F |
probably damaging |
Het |
Rere |
T |
A |
4: 150,701,424 (GRCm39) |
M1268K |
possibly damaging |
Het |
Rp1 |
A |
G |
1: 4,315,318 (GRCm39) |
F485L |
unknown |
Het |
Samd14 |
A |
T |
11: 94,905,213 (GRCm39) |
E8D |
probably benign |
Het |
Serpinh1 |
A |
G |
7: 98,995,545 (GRCm39) |
Y346H |
possibly damaging |
Het |
Shq1 |
A |
T |
6: 100,648,021 (GRCm39) |
M1K |
probably null |
Het |
Tfrc |
T |
C |
16: 32,443,848 (GRCm39) |
S551P |
probably damaging |
Het |
Tnr |
A |
C |
1: 159,715,860 (GRCm39) |
N874T |
possibly damaging |
Het |
Trak1 |
C |
A |
9: 121,298,096 (GRCm39) |
T667N |
probably damaging |
Het |
Trpv2 |
A |
C |
11: 62,481,757 (GRCm39) |
T423P |
probably damaging |
Het |
Ugt1a1 |
CAGAGAGAGAGAGA |
CAGAGAGAGAGA |
1: 88,139,706 (GRCm39) |
|
probably benign |
Het |
Vmn2r24 |
A |
G |
6: 123,756,077 (GRCm39) |
T50A |
probably benign |
Het |
Xirp2 |
T |
A |
2: 67,346,853 (GRCm39) |
D3031E |
probably benign |
Het |
Zbed6 |
G |
T |
1: 133,586,530 (GRCm39) |
A269E |
probably damaging |
Het |
Zbtb47 |
T |
C |
9: 121,596,344 (GRCm39) |
S604P |
probably benign |
Het |
Zfhx3 |
A |
G |
8: 109,677,349 (GRCm39) |
T2800A |
probably benign |
Het |
|
Other mutations in Zbtb4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00592:Zbtb4
|
APN |
11 |
69,667,557 (GRCm39) |
nonsense |
probably null |
|
IGL02178:Zbtb4
|
APN |
11 |
69,667,255 (GRCm39) |
nonsense |
probably null |
|
R0092:Zbtb4
|
UTSW |
11 |
69,670,177 (GRCm39) |
missense |
probably benign |
|
R0403:Zbtb4
|
UTSW |
11 |
69,668,465 (GRCm39) |
missense |
probably damaging |
0.99 |
R1276:Zbtb4
|
UTSW |
11 |
69,667,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R1654:Zbtb4
|
UTSW |
11 |
69,669,995 (GRCm39) |
missense |
probably damaging |
0.98 |
R1734:Zbtb4
|
UTSW |
11 |
69,667,289 (GRCm39) |
missense |
probably benign |
0.13 |
R1762:Zbtb4
|
UTSW |
11 |
69,669,743 (GRCm39) |
missense |
probably benign |
0.03 |
R2224:Zbtb4
|
UTSW |
11 |
69,667,184 (GRCm39) |
missense |
probably benign |
0.43 |
R2930:Zbtb4
|
UTSW |
11 |
69,667,342 (GRCm39) |
nonsense |
probably null |
|
R4670:Zbtb4
|
UTSW |
11 |
69,667,355 (GRCm39) |
missense |
probably damaging |
0.97 |
R4998:Zbtb4
|
UTSW |
11 |
69,669,497 (GRCm39) |
missense |
probably benign |
0.31 |
R5956:Zbtb4
|
UTSW |
11 |
69,669,040 (GRCm39) |
missense |
probably benign |
0.29 |
R5988:Zbtb4
|
UTSW |
11 |
69,669,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R6115:Zbtb4
|
UTSW |
11 |
69,667,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R6237:Zbtb4
|
UTSW |
11 |
69,669,069 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6803:Zbtb4
|
UTSW |
11 |
69,669,454 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7395:Zbtb4
|
UTSW |
11 |
69,666,937 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7756:Zbtb4
|
UTSW |
11 |
69,669,368 (GRCm39) |
missense |
probably benign |
0.27 |
R7758:Zbtb4
|
UTSW |
11 |
69,669,368 (GRCm39) |
missense |
probably benign |
0.27 |
R7877:Zbtb4
|
UTSW |
11 |
69,666,863 (GRCm39) |
missense |
probably benign |
0.39 |
R8306:Zbtb4
|
UTSW |
11 |
69,668,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R8407:Zbtb4
|
UTSW |
11 |
69,669,101 (GRCm39) |
missense |
probably benign |
0.00 |
R8690:Zbtb4
|
UTSW |
11 |
69,667,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R8785:Zbtb4
|
UTSW |
11 |
69,668,989 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9032:Zbtb4
|
UTSW |
11 |
69,672,650 (GRCm39) |
missense |
probably benign |
|
R9674:Zbtb4
|
UTSW |
11 |
69,669,973 (GRCm39) |
missense |
probably damaging |
0.98 |
|