Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931429L15Rik |
A |
T |
9: 46,218,120 (GRCm39) |
I206N |
probably damaging |
Het |
Aadac |
T |
A |
3: 59,947,248 (GRCm39) |
D315E |
probably damaging |
Het |
Abcc8 |
A |
G |
7: 45,773,330 (GRCm39) |
F800L |
probably benign |
Het |
Adamts16 |
C |
A |
13: 70,877,029 (GRCm39) |
C1204F |
probably damaging |
Het |
Adcy7 |
A |
G |
8: 89,038,856 (GRCm39) |
T291A |
possibly damaging |
Het |
AI182371 |
G |
T |
2: 34,976,134 (GRCm39) |
Q255K |
possibly damaging |
Het |
Aig1 |
A |
T |
10: 13,677,528 (GRCm39) |
|
probably benign |
Het |
Ak5 |
T |
C |
3: 152,321,589 (GRCm39) |
D266G |
probably damaging |
Het |
Ank1 |
A |
T |
8: 23,630,220 (GRCm39) |
E93D |
probably damaging |
Het |
Bop1 |
T |
C |
15: 76,340,117 (GRCm39) |
D153G |
probably damaging |
Het |
Bub1 |
G |
T |
2: 127,661,142 (GRCm39) |
N316K |
probably benign |
Het |
Capn1 |
T |
C |
19: 6,047,827 (GRCm39) |
N412S |
probably benign |
Het |
Cdca4 |
A |
G |
12: 112,785,339 (GRCm39) |
S130P |
probably benign |
Het |
Cdh23 |
A |
T |
10: 60,264,158 (GRCm39) |
D663E |
probably damaging |
Het |
Clca3a1 |
T |
C |
3: 144,455,403 (GRCm39) |
|
probably benign |
Het |
Csmd2 |
C |
T |
4: 128,091,178 (GRCm39) |
P239L |
probably damaging |
Het |
Dlg2 |
A |
T |
7: 91,646,579 (GRCm39) |
|
probably benign |
Het |
Dnpep |
C |
T |
1: 75,288,635 (GRCm39) |
|
probably null |
Het |
Dop1b |
A |
T |
16: 93,598,469 (GRCm39) |
H1878L |
probably damaging |
Het |
Dscam |
C |
T |
16: 96,622,120 (GRCm39) |
D444N |
probably damaging |
Het |
Emc9 |
C |
T |
14: 55,819,569 (GRCm39) |
|
probably null |
Het |
Ero1b |
T |
A |
13: 12,615,207 (GRCm39) |
I346N |
probably damaging |
Het |
Etv3 |
A |
G |
3: 87,442,850 (GRCm39) |
T145A |
probably benign |
Het |
Fam170a |
T |
A |
18: 50,415,321 (GRCm39) |
|
probably null |
Het |
Fap |
A |
T |
2: 62,374,700 (GRCm39) |
I261N |
probably damaging |
Het |
Fbn2 |
T |
C |
18: 58,178,409 (GRCm39) |
N1943S |
probably damaging |
Het |
Glb1l3 |
A |
T |
9: 26,737,679 (GRCm39) |
V466E |
probably damaging |
Het |
Gm10521 |
A |
T |
1: 171,724,070 (GRCm39) |
H127L |
unknown |
Het |
Gm8186 |
G |
T |
17: 26,318,130 (GRCm39) |
N22K |
probably damaging |
Het |
Gpr132 |
A |
C |
12: 112,815,717 (GRCm39) |
L370V |
probably benign |
Het |
Hectd1 |
A |
T |
12: 51,845,537 (GRCm39) |
H449Q |
probably damaging |
Het |
Hook3 |
A |
G |
8: 26,534,306 (GRCm39) |
|
probably benign |
Het |
Ift140 |
A |
G |
17: 25,311,345 (GRCm39) |
D1180G |
probably benign |
Het |
Isoc2b |
A |
T |
7: 4,852,577 (GRCm39) |
|
probably null |
Het |
Itga4 |
C |
T |
2: 79,153,000 (GRCm39) |
H896Y |
probably benign |
Het |
Itga7 |
T |
C |
10: 128,778,850 (GRCm39) |
Y326H |
probably damaging |
Het |
Itpr3 |
A |
T |
17: 27,336,867 (GRCm39) |
E2397V |
probably damaging |
Het |
Jtb |
T |
G |
3: 90,142,884 (GRCm39) |
|
probably null |
Het |
Klk15 |
A |
G |
7: 43,588,183 (GRCm39) |
T164A |
probably benign |
Het |
Kmt2e |
C |
A |
5: 23,669,704 (GRCm39) |
H64N |
probably damaging |
Het |
Lamtor3 |
T |
A |
3: 137,633,054 (GRCm39) |
|
probably benign |
Het |
Laptm4b |
A |
G |
15: 34,258,830 (GRCm39) |
I35V |
possibly damaging |
Het |
Lrrc1 |
A |
C |
9: 77,341,379 (GRCm39) |
L393R |
probably damaging |
Het |
Ltn1 |
A |
G |
16: 87,178,391 (GRCm39) |
S1613P |
possibly damaging |
Het |
Mtmr4 |
T |
A |
11: 87,502,876 (GRCm39) |
W920R |
probably damaging |
Het |
Nbeal1 |
T |
C |
1: 60,267,950 (GRCm39) |
|
probably benign |
Het |
Nup133 |
A |
G |
8: 124,643,038 (GRCm39) |
Y761H |
possibly damaging |
Het |
Nwd2 |
T |
A |
5: 63,963,326 (GRCm39) |
V970D |
probably damaging |
Het |
Or4c126 |
A |
G |
2: 89,824,301 (GRCm39) |
H188R |
probably benign |
Het |
Or6n1 |
T |
C |
1: 173,916,785 (GRCm39) |
Y60H |
probably benign |
Het |
Or8k24 |
A |
T |
2: 86,216,218 (GRCm39) |
S181R |
probably damaging |
Het |
Osbp |
C |
T |
19: 11,951,240 (GRCm39) |
L262F |
probably damaging |
Het |
Phf8-ps |
G |
T |
17: 33,285,124 (GRCm39) |
D559E |
probably benign |
Het |
Phldb2 |
G |
T |
16: 45,645,551 (GRCm39) |
D343E |
probably damaging |
Het |
Phrf1 |
T |
A |
7: 140,840,453 (GRCm39) |
M1216K |
possibly damaging |
Het |
Phyh |
A |
T |
2: 4,935,462 (GRCm39) |
|
probably null |
Het |
Plekhf1 |
A |
T |
7: 37,921,594 (GRCm39) |
|
probably null |
Het |
Rars1 |
T |
C |
11: 35,719,475 (GRCm39) |
N116D |
probably damaging |
Het |
Rnf44 |
T |
A |
13: 54,830,621 (GRCm39) |
Q181L |
possibly damaging |
Het |
Rpe65 |
T |
C |
3: 159,321,319 (GRCm39) |
|
probably null |
Het |
Scaf1 |
A |
G |
7: 44,663,016 (GRCm39) |
|
probably benign |
Het |
Serpinb11 |
A |
T |
1: 107,299,919 (GRCm39) |
R88S |
probably benign |
Het |
Slc7a7 |
T |
C |
14: 54,616,560 (GRCm39) |
N174S |
probably damaging |
Het |
Slc9a5 |
T |
C |
8: 106,083,807 (GRCm39) |
|
probably null |
Het |
Slfn1 |
C |
A |
11: 83,012,002 (GRCm39) |
N39K |
possibly damaging |
Het |
Snx20 |
G |
A |
8: 89,353,923 (GRCm39) |
A269V |
possibly damaging |
Het |
Snx6 |
A |
G |
12: 54,801,104 (GRCm39) |
Y298H |
probably damaging |
Het |
Stk32c |
C |
T |
7: 138,700,590 (GRCm39) |
R213Q |
probably benign |
Het |
Tgfbr1 |
A |
T |
4: 47,396,555 (GRCm39) |
I190F |
probably damaging |
Het |
Ube2d2b |
T |
A |
5: 107,978,498 (GRCm39) |
F50I |
probably damaging |
Het |
Ubl5 |
G |
A |
9: 20,557,830 (GRCm39) |
|
probably benign |
Het |
Ubqln5 |
T |
G |
7: 103,777,781 (GRCm39) |
T348P |
possibly damaging |
Het |
Usp46 |
T |
C |
5: 74,197,746 (GRCm39) |
D22G |
probably benign |
Het |
Vars1 |
A |
G |
17: 35,231,352 (GRCm39) |
N655S |
probably damaging |
Het |
Vmn2r103 |
A |
C |
17: 20,032,715 (GRCm39) |
I830L |
possibly damaging |
Het |
Vmn2r26 |
T |
A |
6: 124,016,830 (GRCm39) |
N431K |
probably benign |
Het |
Vmn2r4 |
G |
T |
3: 64,298,487 (GRCm39) |
P547Q |
probably damaging |
Het |
Yy1 |
T |
A |
12: 108,772,354 (GRCm39) |
|
probably benign |
Het |
Zfp12 |
T |
C |
5: 143,225,743 (GRCm39) |
F17S |
probably damaging |
Het |
Zfp219 |
T |
A |
14: 52,244,606 (GRCm39) |
|
probably null |
Het |
Zfp629 |
G |
A |
7: 127,209,542 (GRCm39) |
H756Y |
probably damaging |
Het |
Zfp748 |
T |
C |
13: 67,689,292 (GRCm39) |
K656R |
possibly damaging |
Het |
Zfp958 |
T |
A |
8: 4,679,072 (GRCm39) |
Y366N |
probably benign |
Het |
Zp3 |
C |
T |
5: 136,017,377 (GRCm39) |
T396I |
probably benign |
Het |
|
Other mutations in Zbtb2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01020:Zbtb2
|
APN |
10 |
4,319,702 (GRCm39) |
missense |
probably benign |
0.28 |
IGL02340:Zbtb2
|
APN |
10 |
4,318,712 (GRCm39) |
missense |
probably damaging |
0.98 |
PIT4142001:Zbtb2
|
UTSW |
10 |
4,319,493 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4581001:Zbtb2
|
UTSW |
10 |
4,319,265 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1436:Zbtb2
|
UTSW |
10 |
4,318,697 (GRCm39) |
missense |
probably benign |
0.01 |
R2015:Zbtb2
|
UTSW |
10 |
4,319,757 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2570:Zbtb2
|
UTSW |
10 |
4,318,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R5134:Zbtb2
|
UTSW |
10 |
4,319,267 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5275:Zbtb2
|
UTSW |
10 |
4,318,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R5286:Zbtb2
|
UTSW |
10 |
4,318,566 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5295:Zbtb2
|
UTSW |
10 |
4,318,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R5328:Zbtb2
|
UTSW |
10 |
4,319,267 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5475:Zbtb2
|
UTSW |
10 |
4,319,275 (GRCm39) |
missense |
probably benign |
0.18 |
R5719:Zbtb2
|
UTSW |
10 |
4,319,456 (GRCm39) |
missense |
probably benign |
0.22 |
R6033:Zbtb2
|
UTSW |
10 |
4,318,599 (GRCm39) |
missense |
probably damaging |
0.97 |
R6033:Zbtb2
|
UTSW |
10 |
4,318,599 (GRCm39) |
missense |
probably damaging |
0.97 |
R6492:Zbtb2
|
UTSW |
10 |
4,319,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R7016:Zbtb2
|
UTSW |
10 |
4,318,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R7287:Zbtb2
|
UTSW |
10 |
4,318,986 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7348:Zbtb2
|
UTSW |
10 |
4,324,574 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7486:Zbtb2
|
UTSW |
10 |
4,319,025 (GRCm39) |
nonsense |
probably null |
|
R8316:Zbtb2
|
UTSW |
10 |
4,319,084 (GRCm39) |
missense |
probably benign |
0.02 |
R9031:Zbtb2
|
UTSW |
10 |
4,319,183 (GRCm39) |
missense |
probably damaging |
0.99 |
|