Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm2 |
A |
C |
3: 59,659,449 (GRCm39) |
T301P |
probably damaging |
Het |
Cdc42bpg |
T |
G |
19: 6,365,929 (GRCm39) |
L786R |
probably damaging |
Het |
Cfap73 |
C |
T |
5: 120,767,772 (GRCm39) |
V260I |
probably damaging |
Het |
Chchd10 |
A |
T |
10: 75,773,283 (GRCm39) |
N131I |
probably damaging |
Het |
Clec2l |
C |
T |
6: 38,650,387 (GRCm39) |
T64I |
probably damaging |
Het |
Cpeb3 |
T |
A |
19: 37,151,915 (GRCm39) |
T154S |
probably damaging |
Het |
D130043K22Rik |
A |
G |
13: 25,061,960 (GRCm39) |
E643G |
probably damaging |
Het |
Ddx31 |
A |
G |
2: 28,736,042 (GRCm39) |
M127V |
probably benign |
Het |
Dennd1b |
A |
G |
1: 138,990,615 (GRCm39) |
Y193C |
probably damaging |
Het |
Dgke |
T |
A |
11: 88,941,511 (GRCm39) |
D288V |
probably damaging |
Het |
Dst |
T |
A |
1: 34,247,639 (GRCm39) |
L1683* |
probably null |
Het |
Dusp29 |
G |
A |
14: 21,727,091 (GRCm39) |
R186W |
probably benign |
Het |
E130116L18Rik |
G |
T |
5: 25,428,018 (GRCm39) |
|
probably benign |
Het |
Eif2b5 |
G |
A |
16: 20,320,148 (GRCm39) |
V115I |
possibly damaging |
Het |
Fchsd1 |
C |
T |
18: 38,092,926 (GRCm39) |
|
probably benign |
Het |
Fgfr3 |
A |
T |
5: 33,887,382 (GRCm39) |
T234S |
probably damaging |
Het |
Gipc2 |
A |
T |
3: 151,808,299 (GRCm39) |
D251E |
possibly damaging |
Het |
Gm11787 |
A |
C |
4: 3,511,810 (GRCm39) |
|
noncoding transcript |
Het |
Haus6 |
A |
G |
4: 86,501,415 (GRCm39) |
Y819H |
possibly damaging |
Het |
Homez |
G |
A |
14: 55,095,531 (GRCm39) |
A59V |
probably damaging |
Het |
Iffo1 |
T |
C |
6: 125,129,423 (GRCm39) |
V363A |
probably benign |
Het |
Ifit2 |
T |
A |
19: 34,551,796 (GRCm39) |
D445E |
probably benign |
Het |
Ipo9 |
A |
C |
1: 135,317,344 (GRCm39) |
|
probably benign |
Het |
Kcnv1 |
C |
T |
15: 44,976,640 (GRCm39) |
G216R |
probably damaging |
Het |
Kdm6b |
A |
C |
11: 69,292,730 (GRCm39) |
|
probably benign |
Het |
Mplkip |
T |
C |
13: 17,870,304 (GRCm39) |
S79P |
probably damaging |
Het |
Nae1 |
T |
C |
8: 105,249,776 (GRCm39) |
|
probably benign |
Het |
Nfe2l2 |
A |
T |
2: 75,506,353 (GRCm39) |
N582K |
possibly damaging |
Het |
Nsmce4a |
G |
A |
7: 130,138,754 (GRCm39) |
R297C |
probably damaging |
Het |
Or1e1f |
T |
C |
11: 73,855,632 (GRCm39) |
L66P |
probably damaging |
Het |
Or3a1d |
T |
A |
11: 74,238,068 (GRCm39) |
D114V |
probably damaging |
Het |
Or5p70 |
A |
T |
7: 107,994,909 (GRCm39) |
D194V |
probably damaging |
Het |
Osbp |
T |
A |
19: 11,955,654 (GRCm39) |
F357I |
probably damaging |
Het |
Pcdhb4 |
A |
G |
18: 37,442,979 (GRCm39) |
D763G |
possibly damaging |
Het |
Pcdhgb2 |
A |
C |
18: 37,824,103 (GRCm39) |
I365L |
possibly damaging |
Het |
Pde6g |
A |
G |
11: 120,338,912 (GRCm39) |
|
probably benign |
Het |
Pigo |
C |
A |
4: 43,020,675 (GRCm39) |
V756L |
possibly damaging |
Het |
Pkhd1 |
G |
T |
1: 20,345,865 (GRCm39) |
T2721K |
probably benign |
Het |
Pls1 |
A |
T |
9: 95,658,675 (GRCm39) |
|
probably null |
Het |
Prim2 |
A |
G |
1: 33,519,397 (GRCm39) |
|
probably benign |
Het |
Prkd2 |
T |
A |
7: 16,589,711 (GRCm39) |
I471N |
probably benign |
Het |
Prrc2b |
C |
T |
2: 32,096,408 (GRCm39) |
T593I |
probably benign |
Het |
Ptch2 |
C |
A |
4: 116,963,335 (GRCm39) |
|
probably benign |
Het |
Pth |
A |
T |
7: 112,985,051 (GRCm39) |
D107E |
probably damaging |
Het |
Pycr2 |
A |
C |
1: 180,735,188 (GRCm39) |
Q315P |
probably benign |
Het |
Rbpj |
A |
T |
5: 53,806,782 (GRCm39) |
Y209F |
probably damaging |
Het |
Ripk4 |
C |
A |
16: 97,544,967 (GRCm39) |
R560L |
probably damaging |
Het |
Sdr42e1 |
T |
C |
8: 118,390,021 (GRCm39) |
R207G |
probably benign |
Het |
Sipa1l1 |
A |
G |
12: 82,388,362 (GRCm39) |
Y196C |
possibly damaging |
Het |
Smarcc2 |
T |
C |
10: 128,316,875 (GRCm39) |
|
probably null |
Het |
Stom |
T |
A |
2: 35,226,889 (GRCm39) |
I15F |
probably benign |
Het |
Sugp2 |
G |
T |
8: 70,695,925 (GRCm39) |
L299F |
probably benign |
Het |
Tbrg4 |
A |
T |
11: 6,567,516 (GRCm39) |
|
probably null |
Het |
Tkt |
G |
T |
14: 30,287,635 (GRCm39) |
G210C |
probably damaging |
Het |
Tmem163 |
G |
A |
1: 127,419,289 (GRCm39) |
|
probably benign |
Het |
Trip12 |
A |
G |
1: 84,771,854 (GRCm39) |
I98T |
probably benign |
Het |
Unc5b |
A |
G |
10: 60,610,419 (GRCm39) |
I466T |
probably damaging |
Het |
Unc79 |
T |
A |
12: 103,037,010 (GRCm39) |
F599L |
probably damaging |
Het |
Vav1 |
G |
A |
17: 57,604,122 (GRCm39) |
E151K |
probably damaging |
Het |
Vcan |
T |
G |
13: 89,840,651 (GRCm39) |
D1631A |
probably benign |
Het |
Vmn2r4 |
A |
C |
3: 64,314,358 (GRCm39) |
S208A |
possibly damaging |
Het |
Zfp619 |
A |
G |
7: 39,186,642 (GRCm39) |
T891A |
possibly damaging |
Het |
Zfp672 |
A |
G |
11: 58,220,527 (GRCm39) |
|
probably benign |
Het |
Znhit1 |
T |
A |
5: 137,011,235 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Chn2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00332:Chn2
|
APN |
6 |
54,272,907 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02158:Chn2
|
APN |
6 |
54,277,230 (GRCm39) |
unclassified |
probably benign |
|
IGL02618:Chn2
|
APN |
6 |
54,197,422 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02807:Chn2
|
APN |
6 |
54,272,898 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL03357:Chn2
|
APN |
6 |
54,171,062 (GRCm39) |
missense |
probably benign |
0.02 |
R0002:Chn2
|
UTSW |
6 |
54,250,098 (GRCm39) |
missense |
probably benign |
0.08 |
R0123:Chn2
|
UTSW |
6 |
54,267,436 (GRCm39) |
splice site |
probably benign |
|
R0225:Chn2
|
UTSW |
6 |
54,267,436 (GRCm39) |
splice site |
probably benign |
|
R1478:Chn2
|
UTSW |
6 |
54,270,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R1905:Chn2
|
UTSW |
6 |
54,263,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R3769:Chn2
|
UTSW |
6 |
54,267,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R3946:Chn2
|
UTSW |
6 |
54,246,411 (GRCm39) |
unclassified |
probably benign |
|
R4125:Chn2
|
UTSW |
6 |
54,249,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R4127:Chn2
|
UTSW |
6 |
54,249,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R4128:Chn2
|
UTSW |
6 |
54,249,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R4614:Chn2
|
UTSW |
6 |
54,267,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R4616:Chn2
|
UTSW |
6 |
54,267,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R5063:Chn2
|
UTSW |
6 |
54,267,272 (GRCm39) |
nonsense |
probably null |
|
R5121:Chn2
|
UTSW |
6 |
54,195,546 (GRCm39) |
missense |
possibly damaging |
0.57 |
R5208:Chn2
|
UTSW |
6 |
54,272,786 (GRCm39) |
missense |
probably damaging |
0.97 |
R5348:Chn2
|
UTSW |
6 |
54,277,203 (GRCm39) |
missense |
probably damaging |
0.99 |
R5861:Chn2
|
UTSW |
6 |
54,267,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R6539:Chn2
|
UTSW |
6 |
54,150,446 (GRCm39) |
splice site |
probably null |
|
R6824:Chn2
|
UTSW |
6 |
54,249,938 (GRCm39) |
missense |
probably benign |
0.00 |
R7194:Chn2
|
UTSW |
6 |
54,263,162 (GRCm39) |
splice site |
probably null |
|
R7740:Chn2
|
UTSW |
6 |
54,277,156 (GRCm39) |
missense |
probably benign |
0.18 |
R7765:Chn2
|
UTSW |
6 |
54,275,137 (GRCm39) |
critical splice donor site |
probably null |
|
R7997:Chn2
|
UTSW |
6 |
54,267,270 (GRCm39) |
missense |
probably damaging |
1.00 |
R8477:Chn2
|
UTSW |
6 |
54,246,467 (GRCm39) |
splice site |
probably null |
|
R8804:Chn2
|
UTSW |
6 |
54,250,061 (GRCm39) |
missense |
probably benign |
0.01 |
R9297:Chn2
|
UTSW |
6 |
54,272,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R9318:Chn2
|
UTSW |
6 |
54,272,840 (GRCm39) |
missense |
probably damaging |
1.00 |
|