Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Accsl |
T |
A |
2: 93,688,299 (GRCm39) |
Y445F |
probably benign |
Het |
Actn4 |
T |
C |
7: 28,594,583 (GRCm39) |
D815G |
probably damaging |
Het |
Adam4 |
T |
C |
12: 81,467,146 (GRCm39) |
S492G |
possibly damaging |
Het |
Anapc2 |
A |
G |
2: 25,170,490 (GRCm39) |
K643E |
probably benign |
Het |
Ankfy1 |
T |
A |
11: 72,641,317 (GRCm39) |
I630K |
possibly damaging |
Het |
Arhgap24 |
A |
G |
5: 103,040,136 (GRCm39) |
T361A |
probably benign |
Het |
Arhgef28 |
T |
C |
13: 98,066,141 (GRCm39) |
M1571V |
probably benign |
Het |
Arid5b |
A |
C |
10: 67,937,810 (GRCm39) |
V196G |
possibly damaging |
Het |
Art2b |
C |
A |
7: 101,229,110 (GRCm39) |
|
probably null |
Het |
Asxl3 |
G |
A |
18: 22,650,807 (GRCm39) |
R932H |
probably damaging |
Het |
B3galnt1 |
T |
C |
3: 69,482,673 (GRCm39) |
N196S |
possibly damaging |
Het |
Brd10 |
A |
T |
19: 29,696,126 (GRCm39) |
N1122K |
possibly damaging |
Het |
C5ar2 |
C |
A |
7: 15,971,733 (GRCm39) |
V65F |
possibly damaging |
Het |
Cfap54 |
A |
T |
10: 92,879,255 (GRCm39) |
L403Q |
probably damaging |
Het |
Cfap74 |
G |
A |
4: 155,521,187 (GRCm39) |
E620K |
|
Het |
Chac1 |
C |
T |
2: 119,183,836 (GRCm39) |
A146V |
probably damaging |
Het |
Cux1 |
T |
A |
5: 136,402,203 (GRCm39) |
K138* |
probably null |
Het |
Cwc22 |
T |
A |
2: 77,754,937 (GRCm39) |
Y214F |
probably damaging |
Het |
Cyp2c39 |
A |
T |
19: 39,525,197 (GRCm39) |
T167S |
probably benign |
Het |
Cyp4a12a |
T |
A |
4: 115,185,935 (GRCm39) |
Y414* |
probably null |
Het |
Dap3 |
A |
T |
3: 88,835,570 (GRCm39) |
D256E |
probably damaging |
Het |
Dmxl2 |
C |
T |
9: 54,381,156 (GRCm39) |
S110N |
probably benign |
Het |
Dnhd1 |
A |
T |
7: 105,343,986 (GRCm39) |
I1777L |
probably benign |
Het |
Ecel1 |
G |
A |
1: 87,076,349 (GRCm39) |
Q717* |
probably null |
Het |
Efcab3 |
T |
G |
11: 104,909,525 (GRCm39) |
|
probably null |
Het |
Eif3j2 |
G |
A |
18: 43,610,699 (GRCm39) |
T38M |
possibly damaging |
Het |
Fat3 |
T |
C |
9: 16,287,864 (GRCm39) |
H553R |
probably benign |
Het |
Fcho2 |
T |
C |
13: 98,913,985 (GRCm39) |
D204G |
probably benign |
Het |
Frmpd1 |
A |
T |
4: 45,284,702 (GRCm39) |
E1174D |
probably benign |
Het |
Gabra6 |
T |
A |
11: 42,205,959 (GRCm39) |
Y299F |
probably damaging |
Het |
Gak |
G |
A |
5: 108,777,518 (GRCm39) |
|
probably benign |
Het |
Gapdhs |
T |
A |
7: 30,432,591 (GRCm39) |
H214L |
probably damaging |
Het |
Gapvd1 |
T |
C |
2: 34,568,110 (GRCm39) |
Y1418C |
probably damaging |
Het |
Gk5 |
C |
A |
9: 96,059,562 (GRCm39) |
D471E |
probably benign |
Het |
Glg1 |
A |
G |
8: 111,914,527 (GRCm39) |
M419T |
probably damaging |
Het |
H2ac25 |
T |
A |
11: 58,845,785 (GRCm39) |
N74K |
possibly damaging |
Het |
Ice1 |
T |
C |
13: 70,758,697 (GRCm39) |
N215S |
probably damaging |
Het |
Idh2 |
TCCCAGG |
T |
7: 79,748,079 (GRCm39) |
|
probably benign |
Het |
Ifitm10 |
T |
C |
7: 141,882,300 (GRCm39) |
N157D |
probably benign |
Het |
Itga11 |
A |
G |
9: 62,676,545 (GRCm39) |
D911G |
possibly damaging |
Het |
Kcnt1 |
A |
G |
2: 25,784,338 (GRCm39) |
N247S |
probably benign |
Het |
Kirrel1 |
T |
C |
3: 86,997,173 (GRCm39) |
T265A |
probably benign |
Het |
Klhl29 |
A |
T |
12: 5,187,542 (GRCm39) |
L274H |
possibly damaging |
Het |
Kmt2b |
T |
G |
7: 30,273,640 (GRCm39) |
T2326P |
probably damaging |
Het |
Lcn11 |
A |
G |
2: 25,669,265 (GRCm39) |
S141G |
probably benign |
Het |
Ldb3 |
T |
C |
14: 34,277,301 (GRCm39) |
R358G |
probably null |
Het |
Ldlr |
G |
A |
9: 21,650,828 (GRCm39) |
D446N |
possibly damaging |
Het |
Lipt2 |
T |
C |
7: 99,809,449 (GRCm39) |
F179L |
probably damaging |
Het |
Lmbrd1 |
G |
T |
1: 24,745,121 (GRCm39) |
V154F |
possibly damaging |
Het |
Malrd1 |
A |
G |
2: 15,556,178 (GRCm39) |
I99V |
|
Het |
Map1b |
T |
A |
13: 99,570,735 (GRCm39) |
E662V |
unknown |
Het |
Mfsd11 |
T |
C |
11: 116,750,162 (GRCm39) |
S100P |
probably damaging |
Het |
Mgst1 |
C |
T |
6: 138,119,967 (GRCm39) |
|
probably benign |
Het |
Mtf1 |
T |
A |
4: 124,698,649 (GRCm39) |
V49D |
probably damaging |
Het |
Mtss1 |
T |
C |
15: 58,826,986 (GRCm39) |
D236G |
probably damaging |
Het |
Myct1 |
C |
T |
10: 5,554,208 (GRCm39) |
T25I |
probably damaging |
Het |
Myh4 |
T |
A |
11: 67,143,806 (GRCm39) |
F1089I |
possibly damaging |
Het |
Nrxn1 |
A |
T |
17: 90,897,615 (GRCm39) |
I835K |
probably damaging |
Het |
Nsd3 |
T |
A |
8: 26,163,394 (GRCm39) |
S595T |
probably damaging |
Het |
Nt5c2 |
A |
T |
19: 46,877,361 (GRCm39) |
S527T |
probably damaging |
Het |
Or52m1 |
T |
C |
7: 102,289,882 (GRCm39) |
V143A |
probably benign |
Het |
Or56b2 |
T |
A |
7: 104,337,900 (GRCm39) |
L226* |
probably null |
Het |
Or5k3 |
T |
A |
16: 58,969,319 (GRCm39) |
Y35* |
probably null |
Het |
Or7e175 |
A |
T |
9: 20,048,664 (GRCm39) |
D84V |
probably damaging |
Het |
Or8k28 |
C |
A |
2: 86,285,892 (GRCm39) |
C241F |
probably damaging |
Het |
Osbpl8 |
A |
G |
10: 111,108,053 (GRCm39) |
S350G |
probably benign |
Het |
Otoa |
G |
A |
7: 120,744,741 (GRCm39) |
W833* |
probably null |
Het |
Pcdhga6 |
T |
G |
18: 37,841,540 (GRCm39) |
I420S |
probably damaging |
Het |
Pmfbp1 |
A |
C |
8: 110,258,433 (GRCm39) |
M666L |
probably benign |
Het |
Pola2 |
T |
G |
19: 5,998,452 (GRCm39) |
D370A |
probably damaging |
Het |
Ppip5k1 |
C |
G |
2: 121,153,701 (GRCm39) |
|
probably benign |
Het |
Ppp1r12b |
A |
T |
1: 134,762,200 (GRCm39) |
D815E |
probably benign |
Het |
Ppp4r3b |
T |
A |
11: 29,155,669 (GRCm39) |
V545E |
possibly damaging |
Het |
Ptpn23 |
A |
T |
9: 110,221,568 (GRCm39) |
N177K |
probably damaging |
Het |
Rad9b |
A |
T |
5: 122,482,293 (GRCm39) |
S147R |
probably benign |
Het |
Rps20 |
T |
A |
4: 3,834,617 (GRCm39) |
M82L |
probably benign |
Het |
Samd9l |
C |
T |
6: 3,374,577 (GRCm39) |
V895I |
probably damaging |
Het |
Sbf2 |
T |
A |
7: 110,038,118 (GRCm39) |
K396* |
probably null |
Het |
Sbno2 |
G |
T |
10: 79,893,796 (GRCm39) |
Q1198K |
probably damaging |
Het |
Scp2d1 |
C |
T |
2: 144,665,886 (GRCm39) |
T75I |
probably damaging |
Het |
Shank3 |
T |
A |
15: 89,433,431 (GRCm39) |
I1392N |
possibly damaging |
Het |
Sidt1 |
A |
G |
16: 44,082,390 (GRCm39) |
F532L |
probably benign |
Het |
Smchd1 |
A |
T |
17: 71,755,752 (GRCm39) |
V243D |
probably damaging |
Het |
Smg1 |
T |
C |
7: 117,806,215 (GRCm39) |
R185G |
probably damaging |
Het |
Spag16 |
C |
T |
1: 70,036,004 (GRCm39) |
S344F |
|
Het |
Spata31f3 |
G |
T |
4: 42,871,753 (GRCm39) |
D207E |
probably damaging |
Het |
Spsb3 |
A |
G |
17: 25,110,493 (GRCm39) |
D440G |
probably damaging |
Het |
Themis |
A |
C |
10: 28,665,709 (GRCm39) |
S591R |
probably benign |
Het |
Trpm1 |
G |
A |
7: 63,858,089 (GRCm39) |
V177I |
probably damaging |
Het |
Usp37 |
A |
G |
1: 74,514,143 (GRCm39) |
|
probably null |
Het |
Vmn1r171 |
C |
T |
7: 23,332,525 (GRCm39) |
T238I |
probably damaging |
Het |
Vmn2r33 |
T |
C |
7: 7,554,655 (GRCm39) |
M633V |
probably benign |
Het |
Vmn2r93 |
T |
A |
17: 18,546,252 (GRCm39) |
L708H |
probably damaging |
Het |
Vps35l |
A |
T |
7: 118,393,801 (GRCm39) |
T450S |
possibly damaging |
Het |
Wdr53 |
T |
A |
16: 32,075,473 (GRCm39) |
V226E |
probably damaging |
Het |
Wdr62 |
T |
A |
7: 29,953,454 (GRCm39) |
I193F |
probably damaging |
Het |
Zfp607b |
T |
A |
7: 27,403,387 (GRCm39) |
D614E |
probably benign |
Het |
|
Other mutations in Cpne2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01688:Cpne2
|
APN |
8 |
95,281,381 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL02702:Cpne2
|
APN |
8 |
95,296,651 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03277:Cpne2
|
APN |
8 |
95,275,000 (GRCm39) |
missense |
probably benign |
0.00 |
R0018:Cpne2
|
UTSW |
8 |
95,282,681 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0018:Cpne2
|
UTSW |
8 |
95,282,681 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0126:Cpne2
|
UTSW |
8 |
95,281,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R0135:Cpne2
|
UTSW |
8 |
95,281,553 (GRCm39) |
unclassified |
probably benign |
|
R0167:Cpne2
|
UTSW |
8 |
95,295,207 (GRCm39) |
unclassified |
probably benign |
|
R0661:Cpne2
|
UTSW |
8 |
95,282,667 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0671:Cpne2
|
UTSW |
8 |
95,274,970 (GRCm39) |
start gained |
probably benign |
|
R4691:Cpne2
|
UTSW |
8 |
95,284,849 (GRCm39) |
missense |
probably damaging |
0.99 |
R4856:Cpne2
|
UTSW |
8 |
95,290,592 (GRCm39) |
missense |
probably benign |
0.00 |
R4886:Cpne2
|
UTSW |
8 |
95,290,592 (GRCm39) |
missense |
probably benign |
0.00 |
R6632:Cpne2
|
UTSW |
8 |
95,281,583 (GRCm39) |
missense |
probably benign |
0.00 |
R6699:Cpne2
|
UTSW |
8 |
95,290,587 (GRCm39) |
missense |
probably damaging |
0.99 |
R6968:Cpne2
|
UTSW |
8 |
95,275,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R7117:Cpne2
|
UTSW |
8 |
95,282,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R7505:Cpne2
|
UTSW |
8 |
95,275,094 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7571:Cpne2
|
UTSW |
8 |
95,278,408 (GRCm39) |
missense |
probably benign |
|
R7583:Cpne2
|
UTSW |
8 |
95,282,209 (GRCm39) |
missense |
probably benign |
|
R7612:Cpne2
|
UTSW |
8 |
95,284,048 (GRCm39) |
missense |
probably benign |
0.01 |
R7745:Cpne2
|
UTSW |
8 |
95,295,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R7845:Cpne2
|
UTSW |
8 |
95,277,832 (GRCm39) |
missense |
probably benign |
0.16 |
R8278:Cpne2
|
UTSW |
8 |
95,281,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R8319:Cpne2
|
UTSW |
8 |
95,280,040 (GRCm39) |
missense |
probably benign |
0.01 |
R9082:Cpne2
|
UTSW |
8 |
95,295,237 (GRCm39) |
missense |
probably benign |
0.45 |
R9275:Cpne2
|
UTSW |
8 |
95,281,643 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9588:Cpne2
|
UTSW |
8 |
95,286,781 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9734:Cpne2
|
UTSW |
8 |
95,295,228 (GRCm39) |
missense |
probably benign |
0.34 |
X0025:Cpne2
|
UTSW |
8 |
95,284,079 (GRCm39) |
missense |
probably damaging |
1.00 |
|