Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
T |
A |
7: 119,851,479 (GRCm39) |
M819K |
possibly damaging |
Het |
Adamtsl3 |
T |
G |
7: 82,178,120 (GRCm39) |
C528G |
probably damaging |
Het |
Akap9 |
A |
G |
5: 4,004,870 (GRCm39) |
K148E |
probably benign |
Het |
Akr1b1 |
A |
T |
6: 34,286,577 (GRCm39) |
D225E |
probably benign |
Het |
Alms1 |
C |
A |
6: 85,655,653 (GRCm39) |
Q2931K |
possibly damaging |
Het |
Ano3 |
T |
C |
2: 110,715,346 (GRCm39) |
K31E |
possibly damaging |
Het |
Cdc37 |
A |
G |
9: 21,053,537 (GRCm39) |
I242T |
probably damaging |
Het |
Celsr1 |
T |
A |
15: 85,816,524 (GRCm39) |
K1806N |
possibly damaging |
Het |
Cntnap2 |
A |
T |
6: 47,072,483 (GRCm39) |
Y1017F |
possibly damaging |
Het |
Creb3l2 |
A |
T |
6: 37,311,416 (GRCm39) |
S458T |
probably benign |
Het |
Ctnnd2 |
C |
A |
15: 31,009,230 (GRCm39) |
T1109K |
possibly damaging |
Het |
Dcaf10 |
T |
A |
4: 45,373,011 (GRCm39) |
L425Q |
probably damaging |
Het |
Dlec1 |
A |
G |
9: 118,941,167 (GRCm39) |
E239G |
probably benign |
Het |
Dnah2 |
T |
C |
11: 69,390,020 (GRCm39) |
K742E |
probably damaging |
Het |
Dsp |
A |
T |
13: 38,371,717 (GRCm39) |
R889S |
probably damaging |
Het |
Dync1h1 |
T |
A |
12: 110,599,222 (GRCm39) |
M1859K |
probably damaging |
Het |
Efcab7 |
T |
A |
4: 99,758,886 (GRCm39) |
N361K |
probably damaging |
Het |
Eps8l2 |
T |
C |
7: 140,935,646 (GRCm39) |
V139A |
probably damaging |
Het |
Fads3 |
T |
G |
19: 10,019,200 (GRCm39) |
H35Q |
probably damaging |
Het |
Fam163b |
C |
A |
2: 27,003,583 (GRCm39) |
V24F |
probably damaging |
Het |
Gm14496 |
A |
T |
2: 181,636,904 (GRCm39) |
T121S |
probably benign |
Het |
Gm4799 |
C |
T |
10: 82,790,563 (GRCm39) |
|
noncoding transcript |
Het |
Gm7168 |
A |
T |
17: 14,169,797 (GRCm39) |
D388V |
probably benign |
Het |
Gmeb1 |
A |
T |
4: 131,953,386 (GRCm39) |
L460* |
probably null |
Het |
Gpc6 |
T |
G |
14: 118,212,430 (GRCm39) |
F534V |
probably null |
Het |
Hectd3 |
A |
G |
4: 116,853,241 (GRCm39) |
D156G |
possibly damaging |
Het |
Itga6 |
T |
C |
2: 71,650,404 (GRCm39) |
I150T |
possibly damaging |
Het |
Kansl1 |
A |
G |
11: 104,229,012 (GRCm39) |
M863T |
probably benign |
Het |
Kcnb2 |
A |
T |
1: 15,780,664 (GRCm39) |
Y512F |
probably benign |
Het |
Klhdc2 |
A |
T |
12: 69,347,053 (GRCm39) |
M73L |
probably benign |
Het |
Ktn1 |
A |
G |
14: 47,932,073 (GRCm39) |
T667A |
probably benign |
Het |
Lgsn |
A |
C |
1: 31,242,736 (GRCm39) |
I273L |
probably benign |
Het |
Lilra5 |
A |
G |
7: 4,245,232 (GRCm39) |
D292G |
probably benign |
Het |
Mrps27 |
C |
T |
13: 99,541,582 (GRCm39) |
R229C |
probably damaging |
Het |
Muc5b |
T |
G |
7: 141,416,173 (GRCm39) |
S3040A |
probably benign |
Het |
Nat14 |
T |
C |
7: 4,926,275 (GRCm39) |
S7P |
probably damaging |
Het |
Nfia |
A |
G |
4: 97,671,694 (GRCm39) |
I135V |
possibly damaging |
Het |
Nkd1 |
G |
A |
8: 89,248,944 (GRCm39) |
A30T |
probably damaging |
Het |
Nup205 |
A |
G |
6: 35,202,903 (GRCm39) |
D1370G |
probably null |
Het |
Or1j15 |
C |
G |
2: 36,459,568 (GRCm39) |
|
probably null |
Het |
Or4k15c |
G |
A |
14: 50,321,310 (GRCm39) |
T276I |
probably damaging |
Het |
Or51k2 |
T |
C |
7: 103,596,400 (GRCm39) |
L209P |
probably damaging |
Het |
Or5p79 |
T |
A |
7: 108,221,494 (GRCm39) |
N158K |
possibly damaging |
Het |
Or8s10 |
T |
C |
15: 98,336,168 (GRCm39) |
S273P |
possibly damaging |
Het |
Orc1 |
C |
T |
4: 108,459,229 (GRCm39) |
A466V |
probably benign |
Het |
Otud7a |
T |
A |
7: 63,385,638 (GRCm39) |
D367E |
possibly damaging |
Het |
Pcdhb4 |
A |
G |
18: 37,441,263 (GRCm39) |
Y191C |
probably damaging |
Het |
Pclo |
T |
C |
5: 14,762,828 (GRCm39) |
V3767A |
unknown |
Het |
Pclo |
T |
C |
5: 14,728,789 (GRCm39) |
|
probably benign |
Het |
Prmt1 |
A |
T |
7: 44,628,225 (GRCm39) |
|
probably null |
Het |
Ralgapa1 |
A |
G |
12: 55,842,483 (GRCm39) |
F62S |
probably damaging |
Het |
Rangrf |
T |
C |
11: 68,863,518 (GRCm39) |
S163G |
probably benign |
Het |
Rgs12 |
C |
A |
5: 35,176,804 (GRCm39) |
A65E |
probably damaging |
Het |
Rrbp1 |
T |
C |
2: 143,830,436 (GRCm39) |
N577S |
probably damaging |
Het |
Septin11 |
A |
G |
5: 93,315,393 (GRCm39) |
H374R |
probably damaging |
Het |
Serpina5 |
T |
G |
12: 104,070,046 (GRCm39) |
N314K |
probably benign |
Het |
Sgce |
T |
C |
6: 4,689,621 (GRCm39) |
D395G |
probably damaging |
Het |
Slc26a9 |
A |
T |
1: 131,690,499 (GRCm39) |
N501I |
probably damaging |
Het |
Slc9c1 |
A |
G |
16: 45,401,965 (GRCm39) |
D784G |
possibly damaging |
Het |
Snapc2 |
A |
G |
8: 4,305,676 (GRCm39) |
D207G |
probably benign |
Het |
Stard9 |
G |
T |
2: 120,529,738 (GRCm39) |
M1998I |
probably benign |
Het |
Stk38 |
A |
C |
17: 29,194,907 (GRCm39) |
F280V |
possibly damaging |
Het |
Tas2r126 |
A |
G |
6: 42,412,025 (GRCm39) |
K186R |
probably damaging |
Het |
Tdp1 |
A |
C |
12: 99,875,970 (GRCm39) |
D307A |
probably benign |
Het |
Tead2 |
A |
G |
7: 44,866,674 (GRCm39) |
D11G |
probably damaging |
Het |
Tmco4 |
C |
A |
4: 138,747,383 (GRCm39) |
L211I |
probably damaging |
Het |
Tmem183a |
A |
G |
1: 134,280,115 (GRCm39) |
F255S |
probably damaging |
Het |
Tmem87a |
C |
T |
2: 120,205,929 (GRCm39) |
G349S |
possibly damaging |
Het |
Tpte |
G |
A |
8: 22,826,549 (GRCm39) |
E377K |
possibly damaging |
Het |
Trim32 |
T |
C |
4: 65,531,893 (GRCm39) |
F150S |
possibly damaging |
Het |
Trpc7 |
T |
A |
13: 57,035,636 (GRCm39) |
K99M |
probably damaging |
Het |
Ttc22 |
A |
G |
4: 106,491,381 (GRCm39) |
K195E |
probably damaging |
Het |
Txn2 |
G |
A |
15: 77,811,917 (GRCm39) |
P7S |
probably damaging |
Het |
Ubxn2a |
G |
A |
12: 4,930,700 (GRCm39) |
T220I |
probably damaging |
Het |
Ufd1 |
A |
G |
16: 18,633,626 (GRCm39) |
N17S |
possibly damaging |
Het |
Unc13a |
A |
G |
8: 72,102,509 (GRCm39) |
S958P |
probably damaging |
Het |
Vmn1r202 |
T |
A |
13: 22,685,824 (GRCm39) |
M198L |
probably damaging |
Het |
Vmn2r84 |
G |
A |
10: 130,221,991 (GRCm39) |
A743V |
probably damaging |
Het |
Washc5 |
A |
G |
15: 59,213,007 (GRCm39) |
F891S |
probably damaging |
Het |
Zfp708 |
T |
C |
13: 67,218,375 (GRCm39) |
T495A |
probably benign |
Het |
Zfp81 |
A |
G |
17: 33,553,593 (GRCm39) |
I407T |
probably benign |
Het |
Zswim5 |
T |
C |
4: 116,843,874 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Clpb |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00418:Clpb
|
APN |
7 |
101,436,952 (GRCm39) |
missense |
probably benign |
|
IGL00778:Clpb
|
APN |
7 |
101,427,815 (GRCm39) |
nonsense |
probably null |
|
IGL00780:Clpb
|
APN |
7 |
101,427,815 (GRCm39) |
nonsense |
probably null |
|
IGL00951:Clpb
|
APN |
7 |
101,400,467 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01374:Clpb
|
APN |
7 |
101,422,335 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01542:Clpb
|
APN |
7 |
101,436,712 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02203:Clpb
|
APN |
7 |
101,428,544 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02989:Clpb
|
APN |
7 |
101,428,427 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03088:Clpb
|
APN |
7 |
101,434,656 (GRCm39) |
nonsense |
probably null |
|
Surfeit
|
UTSW |
7 |
101,360,672 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT1430001:Clpb
|
UTSW |
7 |
101,435,926 (GRCm39) |
missense |
possibly damaging |
0.95 |
PIT4486001:Clpb
|
UTSW |
7 |
101,313,139 (GRCm39) |
missense |
probably benign |
0.17 |
R1565:Clpb
|
UTSW |
7 |
101,434,668 (GRCm39) |
missense |
probably benign |
0.00 |
R1760:Clpb
|
UTSW |
7 |
101,435,905 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1879:Clpb
|
UTSW |
7 |
101,355,690 (GRCm39) |
missense |
probably benign |
0.23 |
R1933:Clpb
|
UTSW |
7 |
101,428,418 (GRCm39) |
missense |
probably damaging |
0.96 |
R1938:Clpb
|
UTSW |
7 |
101,412,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R2922:Clpb
|
UTSW |
7 |
101,372,035 (GRCm39) |
missense |
probably benign |
0.02 |
R2923:Clpb
|
UTSW |
7 |
101,372,035 (GRCm39) |
missense |
probably benign |
0.02 |
R2995:Clpb
|
UTSW |
7 |
101,428,531 (GRCm39) |
missense |
probably damaging |
1.00 |
R4492:Clpb
|
UTSW |
7 |
101,436,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R5384:Clpb
|
UTSW |
7 |
101,428,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R5973:Clpb
|
UTSW |
7 |
101,313,204 (GRCm39) |
missense |
probably benign |
0.02 |
R6787:Clpb
|
UTSW |
7 |
101,312,866 (GRCm39) |
unclassified |
probably benign |
|
R7158:Clpb
|
UTSW |
7 |
101,313,039 (GRCm39) |
missense |
probably benign |
0.45 |
R7225:Clpb
|
UTSW |
7 |
101,360,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R7239:Clpb
|
UTSW |
7 |
101,360,662 (GRCm39) |
missense |
probably damaging |
0.96 |
R7482:Clpb
|
UTSW |
7 |
101,435,926 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7499:Clpb
|
UTSW |
7 |
101,371,935 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7547:Clpb
|
UTSW |
7 |
101,313,503 (GRCm39) |
splice site |
probably null |
|
R7769:Clpb
|
UTSW |
7 |
101,371,924 (GRCm39) |
missense |
probably damaging |
0.96 |
R8279:Clpb
|
UTSW |
7 |
101,355,695 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9376:Clpb
|
UTSW |
7 |
101,360,625 (GRCm39) |
missense |
probably benign |
0.01 |
R9501:Clpb
|
UTSW |
7 |
101,427,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R9623:Clpb
|
UTSW |
7 |
101,313,399 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9631:Clpb
|
UTSW |
7 |
101,434,605 (GRCm39) |
missense |
possibly damaging |
0.85 |
|