Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3100002H09Rik |
A |
G |
4: 124,504,316 (GRCm39) |
S79P |
unknown |
Het |
Aadacl4fm2 |
C |
G |
4: 144,281,863 (GRCm39) |
A310P |
probably damaging |
Het |
Adamts20 |
T |
A |
15: 94,238,947 (GRCm39) |
D757V |
probably damaging |
Het |
Adamts9 |
C |
T |
6: 92,784,144 (GRCm39) |
G1570D |
probably damaging |
Het |
Adamtsl3 |
A |
G |
7: 82,077,642 (GRCm39) |
Y109C |
possibly damaging |
Het |
Agl |
G |
A |
3: 116,566,121 (GRCm39) |
R335C |
|
Het |
Ankfy1 |
C |
A |
11: 72,646,532 (GRCm39) |
T805K |
possibly damaging |
Het |
Cast |
A |
T |
13: 74,892,780 (GRCm39) |
V96E |
probably damaging |
Het |
Cdh17 |
G |
T |
4: 11,795,685 (GRCm39) |
E422* |
probably null |
Het |
Cox4i1 |
T |
A |
8: 121,396,110 (GRCm39) |
L21H |
possibly damaging |
Het |
Cwc22 |
T |
C |
2: 77,726,694 (GRCm39) |
E795G |
probably benign |
Het |
Cwf19l2 |
C |
A |
9: 3,430,723 (GRCm39) |
Q352K |
probably benign |
Het |
Cyp2d9 |
T |
C |
15: 82,339,276 (GRCm39) |
V226A |
probably benign |
Het |
Dnah12 |
A |
G |
14: 26,414,757 (GRCm39) |
I53V |
probably benign |
Het |
Dnah7a |
T |
C |
1: 53,674,476 (GRCm39) |
I434V |
probably benign |
Het |
Dock8 |
C |
T |
19: 25,055,448 (GRCm39) |
Q137* |
probably null |
Het |
Far2 |
T |
A |
6: 148,067,133 (GRCm39) |
N339K |
probably benign |
Het |
Gpr22 |
T |
C |
12: 31,759,829 (GRCm39) |
T98A |
probably damaging |
Het |
Hamp2 |
A |
G |
7: 30,621,974 (GRCm39) |
C72R |
probably damaging |
Het |
Hmgn1 |
G |
A |
16: 95,928,540 (GRCm39) |
P16S |
possibly damaging |
Het |
Hspd1 |
A |
G |
1: 55,120,922 (GRCm39) |
S256P |
probably benign |
Het |
Iqcn |
T |
C |
8: 71,162,372 (GRCm39) |
C522R |
possibly damaging |
Het |
Iqgap2 |
T |
C |
13: 95,796,713 (GRCm39) |
H1147R |
probably damaging |
Het |
Itgb1 |
T |
A |
8: 129,439,887 (GRCm39) |
|
probably benign |
Het |
Klhl29 |
A |
T |
12: 5,140,681 (GRCm39) |
W654R |
probably damaging |
Het |
Krtap22-2 |
T |
A |
16: 88,807,514 (GRCm39) |
Y28F |
unknown |
Het |
Lcp2 |
T |
A |
11: 34,004,354 (GRCm39) |
|
probably benign |
Het |
Muc5ac |
T |
G |
7: 141,370,663 (GRCm39) |
L3225R |
possibly damaging |
Het |
Myom3 |
A |
G |
4: 135,523,607 (GRCm39) |
E908G |
possibly damaging |
Het |
Nup54 |
A |
G |
5: 92,570,267 (GRCm39) |
|
probably benign |
Het |
Or1p1 |
T |
A |
11: 74,180,054 (GRCm39) |
I194N |
possibly damaging |
Het |
Or4a74 |
C |
T |
2: 89,440,366 (GRCm39) |
V27I |
probably benign |
Het |
Or51af1 |
T |
C |
7: 103,141,519 (GRCm39) |
T189A |
probably benign |
Het |
Or5ae1 |
T |
A |
7: 84,565,671 (GRCm39) |
I228N |
probably damaging |
Het |
Pak4 |
A |
C |
7: 28,261,969 (GRCm39) |
D453E |
probably benign |
Het |
Pkd1l1 |
T |
C |
11: 8,805,567 (GRCm39) |
T2120A |
|
Het |
Pkhd1l1 |
T |
A |
15: 44,381,570 (GRCm39) |
S1099T |
probably benign |
Het |
Pld2 |
C |
T |
11: 70,444,275 (GRCm39) |
R524W |
probably damaging |
Het |
Polr1a |
T |
A |
6: 71,951,832 (GRCm39) |
D1466E |
probably benign |
Het |
Pxdn |
C |
T |
12: 30,056,601 (GRCm39) |
L1271F |
probably damaging |
Het |
Rp1l1 |
A |
C |
14: 64,269,295 (GRCm39) |
D1627A |
probably damaging |
Het |
Sephs1 |
T |
C |
2: 4,889,402 (GRCm39) |
V60A |
probably benign |
Het |
Sipa1 |
C |
T |
19: 5,710,980 (GRCm39) |
R10Q |
probably damaging |
Het |
Sp4 |
T |
C |
12: 118,263,189 (GRCm39) |
T286A |
possibly damaging |
Het |
Spag5 |
T |
A |
11: 78,192,738 (GRCm39) |
S23R |
probably benign |
Het |
Spag9 |
T |
A |
11: 93,958,916 (GRCm39) |
N313K |
probably benign |
Het |
Stag1 |
T |
A |
9: 100,772,975 (GRCm39) |
|
probably benign |
Het |
Stkld1 |
T |
A |
2: 26,835,817 (GRCm39) |
H217Q |
probably benign |
Het |
Stxbp2 |
T |
A |
8: 3,683,914 (GRCm39) |
F104I |
possibly damaging |
Het |
Tcf12 |
A |
G |
9: 71,765,787 (GRCm39) |
V575A |
possibly damaging |
Het |
Tcf12 |
A |
T |
9: 71,830,069 (GRCm39) |
S131T |
probably benign |
Het |
Tg |
T |
A |
15: 66,553,786 (GRCm39) |
S400R |
probably benign |
Het |
Tomm40 |
T |
C |
7: 19,444,703 (GRCm39) |
T200A |
possibly damaging |
Het |
Trio |
T |
C |
15: 27,919,323 (GRCm39) |
E71G |
unknown |
Het |
Zfp292 |
A |
T |
4: 34,805,982 (GRCm39) |
V2359E |
probably damaging |
Het |
|
Other mutations in Eif4b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01349:Eif4b
|
APN |
15 |
101,999,858 (GRCm39) |
missense |
probably benign |
0.23 |
IGL01896:Eif4b
|
APN |
15 |
102,003,721 (GRCm39) |
missense |
probably benign |
0.23 |
IGL03348:Eif4b
|
APN |
15 |
102,001,466 (GRCm39) |
unclassified |
probably benign |
|
R1577:Eif4b
|
UTSW |
15 |
101,998,336 (GRCm39) |
nonsense |
probably null |
|
R1727:Eif4b
|
UTSW |
15 |
101,998,497 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1931:Eif4b
|
UTSW |
15 |
101,997,411 (GRCm39) |
missense |
unknown |
|
R3927:Eif4b
|
UTSW |
15 |
101,992,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R4051:Eif4b
|
UTSW |
15 |
101,995,039 (GRCm39) |
missense |
probably benign |
0.31 |
R4392:Eif4b
|
UTSW |
15 |
101,995,076 (GRCm39) |
critical splice donor site |
probably null |
|
R5105:Eif4b
|
UTSW |
15 |
101,992,631 (GRCm39) |
missense |
probably benign |
0.42 |
R5716:Eif4b
|
UTSW |
15 |
101,990,494 (GRCm39) |
missense |
probably benign |
0.36 |
R6488:Eif4b
|
UTSW |
15 |
102,001,422 (GRCm39) |
unclassified |
probably benign |
|
R7048:Eif4b
|
UTSW |
15 |
102,001,571 (GRCm39) |
unclassified |
probably benign |
|
R7647:Eif4b
|
UTSW |
15 |
101,997,129 (GRCm39) |
missense |
unknown |
|
R7648:Eif4b
|
UTSW |
15 |
101,997,435 (GRCm39) |
missense |
unknown |
|
R8145:Eif4b
|
UTSW |
15 |
102,001,423 (GRCm39) |
missense |
unknown |
|
R9079:Eif4b
|
UTSW |
15 |
102,003,177 (GRCm39) |
missense |
unknown |
|
R9298:Eif4b
|
UTSW |
15 |
101,990,449 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9716:Eif4b
|
UTSW |
15 |
101,990,443 (GRCm39) |
missense |
probably benign |
0.31 |
|