Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2200002D01Rik |
CCTTCTCCTTCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
CCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
7: 28,947,048 (GRCm39) |
|
probably benign |
Het |
Aass |
T |
C |
6: 23,078,856 (GRCm39) |
T719A |
probably damaging |
Het |
Abcb8 |
A |
G |
5: 24,605,114 (GRCm39) |
E100G |
probably benign |
Het |
Actr1b |
C |
T |
1: 36,741,561 (GRCm39) |
E104K |
probably damaging |
Het |
Atad5 |
T |
A |
11: 79,985,094 (GRCm39) |
S60R |
possibly damaging |
Het |
Bcan |
G |
T |
3: 87,895,610 (GRCm39) |
A842D |
probably benign |
Het |
Cacna2d2 |
G |
A |
9: 107,394,802 (GRCm39) |
E623K |
probably benign |
Het |
Cdk15 |
T |
C |
1: 59,370,142 (GRCm39) |
Y393H |
probably benign |
Het |
Ceacam12 |
C |
T |
7: 17,803,229 (GRCm39) |
R212C |
probably benign |
Het |
Ceacam5 |
T |
C |
7: 17,481,267 (GRCm39) |
I338T |
possibly damaging |
Het |
Crcp |
A |
G |
5: 130,088,664 (GRCm39) |
D139G |
possibly damaging |
Het |
Crls1 |
T |
A |
2: 132,707,802 (GRCm39) |
Y290* |
probably null |
Het |
Dcun1d5 |
A |
G |
9: 7,206,780 (GRCm39) |
N206D |
probably damaging |
Het |
Dmtf1 |
A |
T |
5: 9,190,399 (GRCm39) |
V105E |
possibly damaging |
Het |
Dnah7a |
T |
C |
1: 53,543,474 (GRCm39) |
Y2232C |
probably benign |
Het |
Dnajc25 |
T |
A |
4: 59,003,394 (GRCm39) |
V55E |
probably damaging |
Het |
Dpy19l4 |
T |
C |
4: 11,303,343 (GRCm39) |
M193V |
possibly damaging |
Het |
Dsc1 |
A |
T |
18: 20,221,489 (GRCm39) |
V662E |
probably damaging |
Het |
Enpp6 |
G |
A |
8: 47,506,627 (GRCm39) |
V144I |
possibly damaging |
Het |
Fip1l1 |
A |
G |
5: 74,707,463 (GRCm39) |
T204A |
possibly damaging |
Het |
Flvcr2 |
T |
C |
12: 85,793,795 (GRCm39) |
V57A |
probably benign |
Het |
Fsip2 |
T |
G |
2: 82,822,756 (GRCm39) |
I6163S |
possibly damaging |
Het |
Gipr |
T |
A |
7: 18,896,863 (GRCm39) |
M136L |
probably benign |
Het |
Gm7298 |
A |
G |
6: 121,748,746 (GRCm39) |
I674V |
probably benign |
Het |
Gtf2a1 |
C |
T |
12: 91,534,592 (GRCm39) |
V221I |
probably damaging |
Het |
Haus3 |
A |
T |
5: 34,321,002 (GRCm39) |
D481E |
probably benign |
Het |
Hinfp |
A |
C |
9: 44,209,083 (GRCm39) |
V345G |
probably damaging |
Het |
Hs3st5 |
A |
T |
10: 36,708,698 (GRCm39) |
K78* |
probably null |
Het |
Ighv1-31 |
T |
C |
12: 114,792,894 (GRCm39) |
Y114C |
probably damaging |
Het |
Ighv5-15 |
T |
A |
12: 113,790,357 (GRCm39) |
T88S |
probably damaging |
Het |
Ildr1 |
G |
A |
16: 36,542,721 (GRCm39) |
D418N |
probably damaging |
Het |
Ints10 |
C |
T |
8: 69,271,967 (GRCm39) |
T556I |
probably damaging |
Het |
Isoc1 |
G |
T |
18: 58,792,757 (GRCm39) |
R65L |
possibly damaging |
Het |
Itm2c |
C |
T |
1: 85,833,055 (GRCm39) |
R130C |
probably damaging |
Het |
Jup |
C |
T |
11: 100,270,391 (GRCm39) |
C372Y |
probably damaging |
Het |
Kif11 |
T |
C |
19: 37,399,892 (GRCm39) |
V793A |
probably benign |
Het |
Klrg1 |
A |
C |
6: 122,256,699 (GRCm39) |
V29G |
probably benign |
Het |
Lrch4 |
A |
G |
5: 137,631,953 (GRCm39) |
T114A |
possibly damaging |
Het |
Map3k3 |
C |
T |
11: 106,033,335 (GRCm39) |
T196M |
probably damaging |
Het |
Marchf1 |
C |
A |
8: 66,921,145 (GRCm39) |
T274N |
probably benign |
Het |
Nxpe5 |
A |
T |
5: 138,249,445 (GRCm39) |
T412S |
probably benign |
Het |
Or10q1 |
C |
T |
19: 13,727,069 (GRCm39) |
H200Y |
probably benign |
Het |
Pcnt |
A |
G |
10: 76,258,960 (GRCm39) |
W502R |
probably damaging |
Het |
Pfdn5 |
T |
C |
15: 102,235,286 (GRCm39) |
|
probably null |
Het |
Pkn2 |
A |
T |
3: 142,535,018 (GRCm39) |
V232E |
probably damaging |
Het |
Ppfibp1 |
T |
C |
6: 146,898,307 (GRCm39) |
S88P |
probably damaging |
Het |
Prr23a4 |
A |
G |
9: 98,785,478 (GRCm39) |
I48V |
probably benign |
Het |
Ptprz1 |
G |
A |
6: 23,045,706 (GRCm39) |
E2159K |
probably damaging |
Het |
Smyd3 |
T |
C |
1: 178,871,470 (GRCm39) |
E303G |
possibly damaging |
Het |
Snx13 |
T |
A |
12: 35,151,048 (GRCm39) |
N336K |
possibly damaging |
Het |
Src |
A |
G |
2: 157,311,808 (GRCm39) |
E512G |
possibly damaging |
Het |
Stard9 |
T |
A |
2: 120,495,420 (GRCm39) |
C98* |
probably null |
Het |
Tapbpl |
A |
G |
6: 125,203,672 (GRCm39) |
V336A |
probably benign |
Het |
Tbrg1 |
G |
A |
9: 37,563,945 (GRCm39) |
T230I |
probably damaging |
Het |
Tm7sf3 |
C |
T |
6: 146,525,179 (GRCm39) |
D89N |
possibly damaging |
Het |
Tmem132c |
G |
A |
5: 127,640,145 (GRCm39) |
G772D |
probably damaging |
Het |
Tmem219 |
C |
T |
7: 126,496,017 (GRCm39) |
G119S |
possibly damaging |
Het |
Ttbk2 |
T |
A |
2: 120,603,766 (GRCm39) |
S325C |
probably benign |
Het |
Ttc28 |
A |
T |
5: 111,331,073 (GRCm39) |
Y431F |
probably benign |
Het |
Vmn1r27 |
A |
T |
6: 58,192,746 (GRCm39) |
M86K |
possibly damaging |
Het |
Vmn2r15 |
G |
A |
5: 109,441,953 (GRCm39) |
P160L |
possibly damaging |
Het |
Zfc3h1 |
A |
T |
10: 115,221,223 (GRCm39) |
S41C |
unknown |
Het |
Zfp260 |
C |
A |
7: 29,804,232 (GRCm39) |
T44K |
probably benign |
Het |
Zfp7 |
TGCGGGAAAGGTTTCCACCTGAGCG |
TGCG |
15: 76,774,800 (GRCm39) |
|
probably benign |
Het |
Zfp788 |
T |
A |
7: 41,299,708 (GRCm39) |
Y781* |
probably null |
Het |
Zfp800 |
A |
T |
6: 28,256,433 (GRCm39) |
S52T |
possibly damaging |
Het |
|
Other mutations in Zfp760 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00472:Zfp760
|
APN |
17 |
21,942,457 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL00862:Zfp760
|
APN |
17 |
21,941,265 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02198:Zfp760
|
APN |
17 |
21,941,193 (GRCm39) |
missense |
probably benign |
0.00 |
R0478:Zfp760
|
UTSW |
17 |
21,940,995 (GRCm39) |
nonsense |
probably null |
|
R0835:Zfp760
|
UTSW |
17 |
21,942,559 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1191:Zfp760
|
UTSW |
17 |
21,942,286 (GRCm39) |
missense |
probably damaging |
1.00 |
R1760:Zfp760
|
UTSW |
17 |
21,941,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R2698:Zfp760
|
UTSW |
17 |
21,939,935 (GRCm39) |
missense |
probably damaging |
0.99 |
R3722:Zfp760
|
UTSW |
17 |
21,941,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R4561:Zfp760
|
UTSW |
17 |
21,942,648 (GRCm39) |
missense |
probably benign |
0.00 |
R4700:Zfp760
|
UTSW |
17 |
21,941,388 (GRCm39) |
missense |
probably benign |
0.01 |
R4859:Zfp760
|
UTSW |
17 |
21,942,516 (GRCm39) |
nonsense |
probably null |
|
R4859:Zfp760
|
UTSW |
17 |
21,942,511 (GRCm39) |
missense |
probably damaging |
0.97 |
R4897:Zfp760
|
UTSW |
17 |
21,942,229 (GRCm39) |
missense |
probably benign |
0.02 |
R6675:Zfp760
|
UTSW |
17 |
21,941,991 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7286:Zfp760
|
UTSW |
17 |
21,941,760 (GRCm39) |
missense |
probably benign |
0.04 |
R7336:Zfp760
|
UTSW |
17 |
21,942,814 (GRCm39) |
missense |
unknown |
|
R7356:Zfp760
|
UTSW |
17 |
21,941,601 (GRCm39) |
missense |
probably benign |
|
R7369:Zfp760
|
UTSW |
17 |
21,942,214 (GRCm39) |
missense |
probably benign |
0.00 |
R7504:Zfp760
|
UTSW |
17 |
21,941,655 (GRCm39) |
missense |
probably damaging |
0.97 |
R7553:Zfp760
|
UTSW |
17 |
21,941,872 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7577:Zfp760
|
UTSW |
17 |
21,941,242 (GRCm39) |
nonsense |
probably null |
|
R7579:Zfp760
|
UTSW |
17 |
21,941,907 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7608:Zfp760
|
UTSW |
17 |
21,941,797 (GRCm39) |
missense |
probably benign |
0.00 |
R7973:Zfp760
|
UTSW |
17 |
21,941,084 (GRCm39) |
missense |
probably benign |
0.00 |
R8078:Zfp760
|
UTSW |
17 |
21,942,436 (GRCm39) |
missense |
probably benign |
0.27 |
R8332:Zfp760
|
UTSW |
17 |
21,942,301 (GRCm39) |
missense |
probably damaging |
0.99 |
R8750:Zfp760
|
UTSW |
17 |
21,941,356 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9094:Zfp760
|
UTSW |
17 |
21,941,932 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9264:Zfp760
|
UTSW |
17 |
21,942,663 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9520:Zfp760
|
UTSW |
17 |
21,941,036 (GRCm39) |
missense |
probably benign |
0.00 |
R9564:Zfp760
|
UTSW |
17 |
21,942,272 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9743:Zfp760
|
UTSW |
17 |
21,942,338 (GRCm39) |
missense |
probably benign |
|
X0057:Zfp760
|
UTSW |
17 |
21,942,663 (GRCm39) |
missense |
possibly damaging |
0.80 |
|