Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca7 |
T |
A |
10: 79,837,463 (GRCm39) |
L449Q |
probably benign |
Het |
Agtpbp1 |
T |
C |
13: 59,652,067 (GRCm39) |
T415A |
probably benign |
Het |
Akt3 |
A |
T |
1: 176,924,600 (GRCm39) |
V165D |
probably damaging |
Het |
Cbr2 |
T |
A |
11: 120,620,628 (GRCm39) |
I219F |
probably damaging |
Het |
Cdh20 |
T |
A |
1: 104,902,768 (GRCm39) |
D486E |
probably damaging |
Het |
Cenpe |
A |
G |
3: 134,949,523 (GRCm39) |
S103G |
possibly damaging |
Het |
Chd4 |
T |
A |
6: 125,105,836 (GRCm39) |
S1818T |
probably benign |
Het |
Chst5 |
T |
C |
8: 112,616,795 (GRCm39) |
D275G |
probably damaging |
Het |
Clca3a1 |
A |
G |
3: 144,724,328 (GRCm39) |
I244T |
probably damaging |
Het |
Cyp2c54 |
A |
G |
19: 40,058,716 (GRCm39) |
Y239H |
probably benign |
Het |
Czib |
T |
G |
4: 107,752,097 (GRCm39) |
S159A |
probably benign |
Het |
Ddx25 |
A |
G |
9: 35,454,951 (GRCm39) |
F446L |
possibly damaging |
Het |
Dgkb |
T |
C |
12: 38,186,646 (GRCm39) |
L265P |
probably damaging |
Het |
Dis3 |
A |
G |
14: 99,327,415 (GRCm39) |
S363P |
probably benign |
Het |
Disp3 |
T |
C |
4: 148,327,323 (GRCm39) |
E1187G |
probably damaging |
Het |
Dop1b |
G |
A |
16: 93,603,249 (GRCm39) |
G2061R |
probably damaging |
Het |
Dsp |
T |
C |
13: 38,376,765 (GRCm39) |
S1517P |
probably benign |
Het |
Epg5 |
T |
A |
18: 78,076,141 (GRCm39) |
V2513E |
probably benign |
Het |
Fryl |
T |
A |
5: 73,255,539 (GRCm39) |
T831S |
probably benign |
Het |
Gm6309 |
A |
T |
5: 146,105,100 (GRCm39) |
V271D |
probably damaging |
Het |
H2-M2 |
G |
T |
17: 37,793,528 (GRCm39) |
S159R |
probably benign |
Het |
Helq |
A |
G |
5: 100,937,999 (GRCm39) |
|
probably null |
Het |
Herc1 |
G |
C |
9: 66,382,135 (GRCm39) |
D3621H |
probably damaging |
Het |
Hsd11b2 |
A |
T |
8: 106,245,755 (GRCm39) |
I87F |
probably damaging |
Het |
Ice2 |
A |
G |
9: 69,339,360 (GRCm39) |
N959S |
probably damaging |
Het |
Ifi47 |
T |
A |
11: 48,987,452 (GRCm39) |
D406E |
probably damaging |
Het |
Ifit3 |
T |
G |
19: 34,565,280 (GRCm39) |
S275R |
probably damaging |
Het |
Insl5 |
C |
A |
4: 102,875,395 (GRCm39) |
K118N |
probably damaging |
Het |
Irf7 |
A |
T |
7: 140,844,550 (GRCm39) |
F158I |
probably benign |
Het |
Kat2b |
T |
C |
17: 53,931,431 (GRCm39) |
L143P |
probably damaging |
Het |
Klk1b1 |
A |
T |
7: 43,619,746 (GRCm39) |
N102Y |
probably damaging |
Het |
Krt13 |
C |
T |
11: 100,008,824 (GRCm39) |
G410S |
unknown |
Het |
Larp6 |
A |
T |
9: 60,631,437 (GRCm39) |
T70S |
probably benign |
Het |
Lrrc37a |
T |
C |
11: 103,392,683 (GRCm39) |
E914G |
possibly damaging |
Het |
Mindy4 |
T |
C |
6: 55,274,738 (GRCm39) |
|
probably null |
Het |
Myl10 |
G |
C |
5: 136,726,825 (GRCm39) |
V70L |
probably benign |
Het |
Myom2 |
A |
G |
8: 15,167,679 (GRCm39) |
Y1088C |
probably damaging |
Het |
Mysm1 |
T |
C |
4: 94,840,452 (GRCm39) |
N655D |
probably benign |
Het |
Nbas |
T |
A |
12: 13,329,390 (GRCm39) |
S112T |
probably damaging |
Het |
Neb |
A |
G |
2: 52,055,115 (GRCm39) |
|
probably null |
Het |
Noxred1 |
G |
A |
12: 87,280,206 (GRCm39) |
A42V |
probably benign |
Het |
Olfm5 |
G |
A |
7: 103,803,444 (GRCm39) |
P340S |
possibly damaging |
Het |
Or11h4 |
G |
A |
14: 50,974,122 (GRCm39) |
P166S |
probably benign |
Het |
Or2l5 |
T |
C |
16: 19,333,544 (GRCm39) |
T281A |
probably damaging |
Het |
Or5al5 |
A |
G |
2: 85,961,608 (GRCm39) |
V133A |
probably benign |
Het |
Or5m8 |
T |
A |
2: 85,822,245 (GRCm39) |
V28E |
probably benign |
Het |
Or9i1b |
A |
G |
19: 13,896,449 (GRCm39) |
K22E |
probably benign |
Het |
Pccb |
A |
T |
9: 100,876,615 (GRCm39) |
|
probably null |
Het |
Pnn |
T |
A |
12: 59,118,923 (GRCm39) |
V502E |
probably benign |
Het |
Pole2 |
A |
T |
12: 69,269,203 (GRCm39) |
I98K |
probably benign |
Het |
Ptpn18 |
G |
A |
1: 34,512,445 (GRCm39) |
D417N |
possibly damaging |
Het |
Rasgrp4 |
A |
G |
7: 28,838,484 (GRCm39) |
K111E |
probably benign |
Het |
Rbbp6 |
G |
A |
7: 122,589,366 (GRCm39) |
M351I |
probably benign |
Het |
Rgs19 |
T |
G |
2: 181,333,101 (GRCm39) |
H53P |
probably damaging |
Het |
Rin1 |
A |
T |
19: 5,102,564 (GRCm39) |
T369S |
probably benign |
Het |
Rnaset2b |
G |
A |
17: 7,259,138 (GRCm39) |
E135K |
possibly damaging |
Het |
Rprd2 |
G |
A |
3: 95,683,899 (GRCm39) |
P379S |
probably damaging |
Het |
Sbno1 |
A |
G |
5: 124,551,342 (GRCm39) |
L47P |
possibly damaging |
Het |
Slamf6 |
T |
A |
1: 171,747,325 (GRCm39) |
L29Q |
unknown |
Het |
Slc16a14 |
T |
C |
1: 84,890,843 (GRCm39) |
Y154C |
probably damaging |
Het |
Slc22a29 |
A |
G |
19: 8,147,342 (GRCm39) |
F340S |
probably damaging |
Het |
Slc6a4 |
T |
G |
11: 76,905,976 (GRCm39) |
I259S |
possibly damaging |
Het |
Smarca4 |
G |
A |
9: 21,558,921 (GRCm39) |
V651I |
possibly damaging |
Het |
Susd5 |
C |
T |
9: 113,893,108 (GRCm39) |
A62V |
possibly damaging |
Het |
Syt1 |
T |
A |
10: 108,463,283 (GRCm39) |
|
probably null |
Het |
Taf10 |
T |
C |
7: 105,390,117 (GRCm39) |
I218T |
probably benign |
Het |
Tas1r1 |
C |
A |
4: 152,112,819 (GRCm39) |
V745F |
probably benign |
Het |
Tas2r125 |
C |
A |
6: 132,887,287 (GRCm39) |
T225K |
probably damaging |
Het |
Tcp11l2 |
G |
T |
10: 84,430,523 (GRCm39) |
R216L |
possibly damaging |
Het |
Tnks1bp1 |
C |
T |
2: 84,893,624 (GRCm39) |
Q1184* |
probably null |
Het |
Treml2 |
T |
A |
17: 48,609,847 (GRCm39) |
V93D |
probably damaging |
Het |
Trim11 |
G |
A |
11: 58,872,891 (GRCm39) |
E192K |
probably damaging |
Het |
Trim43a |
A |
G |
9: 88,470,201 (GRCm39) |
K336E |
probably damaging |
Het |
Tspan33 |
T |
A |
6: 29,717,588 (GRCm39) |
I268N |
possibly damaging |
Het |
Tstd2 |
C |
T |
4: 46,116,960 (GRCm39) |
C458Y |
probably damaging |
Het |
Ttc6 |
A |
G |
12: 57,623,305 (GRCm39) |
S235G |
probably benign |
Het |
Usp29 |
A |
C |
7: 6,964,219 (GRCm39) |
T21P |
possibly damaging |
Het |
Usp36 |
A |
T |
11: 118,152,872 (GRCm39) |
S1084T |
possibly damaging |
Het |
Vps39 |
T |
A |
2: 120,155,176 (GRCm39) |
N550I |
probably damaging |
Het |
Wdr47 |
A |
G |
3: 108,537,027 (GRCm39) |
I572V |
probably benign |
Het |
Zfp112 |
A |
T |
7: 23,826,135 (GRCm39) |
Y705F |
probably damaging |
Het |
Zfp282 |
A |
G |
6: 47,881,878 (GRCm39) |
T522A |
probably benign |
Het |
Zfp90 |
A |
T |
8: 107,150,900 (GRCm39) |
K204N |
possibly damaging |
Het |
Zmym2 |
T |
C |
14: 57,194,536 (GRCm39) |
S1265P |
probably damaging |
Het |
|
Other mutations in Zfp292 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00401:Zfp292
|
APN |
4 |
34,808,683 (GRCm39) |
missense |
probably benign |
0.15 |
IGL00502:Zfp292
|
APN |
4 |
34,809,775 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL00539:Zfp292
|
APN |
4 |
34,808,790 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00676:Zfp292
|
APN |
4 |
34,807,827 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01068:Zfp292
|
APN |
4 |
34,806,763 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01311:Zfp292
|
APN |
4 |
34,807,961 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01639:Zfp292
|
APN |
4 |
34,809,048 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01688:Zfp292
|
APN |
4 |
34,807,855 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02345:Zfp292
|
APN |
4 |
34,809,244 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02444:Zfp292
|
APN |
4 |
34,808,810 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02548:Zfp292
|
APN |
4 |
34,805,416 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02551:Zfp292
|
APN |
4 |
34,806,462 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02702:Zfp292
|
APN |
4 |
34,809,415 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02715:Zfp292
|
APN |
4 |
34,819,542 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03273:Zfp292
|
APN |
4 |
34,806,163 (GRCm39) |
missense |
probably benign |
0.00 |
F5770:Zfp292
|
UTSW |
4 |
34,806,783 (GRCm39) |
missense |
possibly damaging |
0.85 |
PIT4362001:Zfp292
|
UTSW |
4 |
34,807,524 (GRCm39) |
missense |
probably benign |
0.00 |
R0153:Zfp292
|
UTSW |
4 |
34,811,185 (GRCm39) |
missense |
probably benign |
0.26 |
R0184:Zfp292
|
UTSW |
4 |
34,819,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R0295:Zfp292
|
UTSW |
4 |
34,806,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R0367:Zfp292
|
UTSW |
4 |
34,808,227 (GRCm39) |
missense |
probably benign |
0.25 |
R0433:Zfp292
|
UTSW |
4 |
34,839,959 (GRCm39) |
missense |
probably damaging |
0.99 |
R0481:Zfp292
|
UTSW |
4 |
34,810,059 (GRCm39) |
missense |
probably benign |
0.28 |
R0555:Zfp292
|
UTSW |
4 |
34,807,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R0597:Zfp292
|
UTSW |
4 |
34,807,399 (GRCm39) |
missense |
probably benign |
0.02 |
R0748:Zfp292
|
UTSW |
4 |
34,816,424 (GRCm39) |
splice site |
probably benign |
|
R0782:Zfp292
|
UTSW |
4 |
34,839,382 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0834:Zfp292
|
UTSW |
4 |
34,809,114 (GRCm39) |
missense |
probably benign |
0.00 |
R0879:Zfp292
|
UTSW |
4 |
34,811,218 (GRCm39) |
missense |
probably benign |
0.00 |
R1083:Zfp292
|
UTSW |
4 |
34,807,569 (GRCm39) |
missense |
probably damaging |
0.98 |
R1343:Zfp292
|
UTSW |
4 |
34,805,238 (GRCm39) |
missense |
probably damaging |
0.98 |
R1498:Zfp292
|
UTSW |
4 |
34,805,397 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1714:Zfp292
|
UTSW |
4 |
34,808,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R1724:Zfp292
|
UTSW |
4 |
34,811,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R1755:Zfp292
|
UTSW |
4 |
34,811,043 (GRCm39) |
missense |
probably benign |
0.02 |
R1837:Zfp292
|
UTSW |
4 |
34,810,264 (GRCm39) |
missense |
probably damaging |
0.98 |
R1914:Zfp292
|
UTSW |
4 |
34,805,100 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1915:Zfp292
|
UTSW |
4 |
34,805,100 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1936:Zfp292
|
UTSW |
4 |
34,807,452 (GRCm39) |
missense |
probably benign |
0.22 |
R2107:Zfp292
|
UTSW |
4 |
34,808,593 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2108:Zfp292
|
UTSW |
4 |
34,808,593 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2136:Zfp292
|
UTSW |
4 |
34,810,266 (GRCm39) |
missense |
probably benign |
0.13 |
R2182:Zfp292
|
UTSW |
4 |
34,807,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R2186:Zfp292
|
UTSW |
4 |
34,807,962 (GRCm39) |
missense |
probably benign |
0.07 |
R2306:Zfp292
|
UTSW |
4 |
34,809,468 (GRCm39) |
missense |
probably damaging |
0.96 |
R2350:Zfp292
|
UTSW |
4 |
34,811,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R2382:Zfp292
|
UTSW |
4 |
34,806,426 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2872:Zfp292
|
UTSW |
4 |
34,808,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R2872:Zfp292
|
UTSW |
4 |
34,808,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R3018:Zfp292
|
UTSW |
4 |
34,808,814 (GRCm39) |
missense |
probably damaging |
0.99 |
R3812:Zfp292
|
UTSW |
4 |
34,810,326 (GRCm39) |
missense |
probably damaging |
0.98 |
R4006:Zfp292
|
UTSW |
4 |
34,807,744 (GRCm39) |
missense |
probably benign |
0.00 |
R4006:Zfp292
|
UTSW |
4 |
34,809,611 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4060:Zfp292
|
UTSW |
4 |
34,810,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R4062:Zfp292
|
UTSW |
4 |
34,810,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R4063:Zfp292
|
UTSW |
4 |
34,810,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R4064:Zfp292
|
UTSW |
4 |
34,810,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R4207:Zfp292
|
UTSW |
4 |
34,806,079 (GRCm39) |
missense |
probably benign |
0.04 |
R4641:Zfp292
|
UTSW |
4 |
34,807,828 (GRCm39) |
missense |
probably damaging |
0.99 |
R4684:Zfp292
|
UTSW |
4 |
34,807,078 (GRCm39) |
missense |
probably benign |
0.00 |
R4718:Zfp292
|
UTSW |
4 |
34,819,521 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4865:Zfp292
|
UTSW |
4 |
34,819,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R4870:Zfp292
|
UTSW |
4 |
34,808,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R5097:Zfp292
|
UTSW |
4 |
34,839,878 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5233:Zfp292
|
UTSW |
4 |
34,809,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R5246:Zfp292
|
UTSW |
4 |
34,805,842 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5369:Zfp292
|
UTSW |
4 |
34,807,491 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5527:Zfp292
|
UTSW |
4 |
34,806,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R5621:Zfp292
|
UTSW |
4 |
34,811,703 (GRCm39) |
missense |
probably damaging |
0.98 |
R5770:Zfp292
|
UTSW |
4 |
34,806,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R5900:Zfp292
|
UTSW |
4 |
34,805,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R5905:Zfp292
|
UTSW |
4 |
34,819,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R5994:Zfp292
|
UTSW |
4 |
34,805,464 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6028:Zfp292
|
UTSW |
4 |
34,819,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R6056:Zfp292
|
UTSW |
4 |
34,809,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R6093:Zfp292
|
UTSW |
4 |
34,811,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R6126:Zfp292
|
UTSW |
4 |
34,808,497 (GRCm39) |
missense |
probably benign |
0.13 |
R6209:Zfp292
|
UTSW |
4 |
34,809,442 (GRCm39) |
missense |
probably benign |
0.14 |
R6275:Zfp292
|
UTSW |
4 |
34,808,883 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6523:Zfp292
|
UTSW |
4 |
34,816,301 (GRCm39) |
missense |
probably benign |
0.21 |
R6747:Zfp292
|
UTSW |
4 |
34,806,894 (GRCm39) |
missense |
probably damaging |
0.97 |
R6752:Zfp292
|
UTSW |
4 |
34,808,593 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6967:Zfp292
|
UTSW |
4 |
34,807,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R7038:Zfp292
|
UTSW |
4 |
34,816,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R7056:Zfp292
|
UTSW |
4 |
34,809,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R7088:Zfp292
|
UTSW |
4 |
34,806,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R7158:Zfp292
|
UTSW |
4 |
34,808,679 (GRCm39) |
missense |
probably benign |
|
R7254:Zfp292
|
UTSW |
4 |
34,819,476 (GRCm39) |
missense |
probably damaging |
0.98 |
R7350:Zfp292
|
UTSW |
4 |
34,806,839 (GRCm39) |
missense |
probably benign |
|
R7378:Zfp292
|
UTSW |
4 |
34,808,384 (GRCm39) |
missense |
probably benign |
0.26 |
R7589:Zfp292
|
UTSW |
4 |
34,806,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R7816:Zfp292
|
UTSW |
4 |
34,809,865 (GRCm39) |
missense |
probably benign |
0.02 |
R7979:Zfp292
|
UTSW |
4 |
34,809,198 (GRCm39) |
missense |
probably benign |
0.02 |
R7997:Zfp292
|
UTSW |
4 |
34,808,688 (GRCm39) |
missense |
probably damaging |
0.96 |
R8129:Zfp292
|
UTSW |
4 |
34,807,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R8211:Zfp292
|
UTSW |
4 |
34,806,163 (GRCm39) |
missense |
probably benign |
0.00 |
R8302:Zfp292
|
UTSW |
4 |
34,810,893 (GRCm39) |
missense |
possibly damaging |
0.64 |
R8500:Zfp292
|
UTSW |
4 |
34,826,691 (GRCm39) |
critical splice donor site |
probably null |
|
R8709:Zfp292
|
UTSW |
4 |
34,805,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R8947:Zfp292
|
UTSW |
4 |
34,811,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R9099:Zfp292
|
UTSW |
4 |
34,809,228 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9190:Zfp292
|
UTSW |
4 |
34,819,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R9256:Zfp292
|
UTSW |
4 |
34,839,899 (GRCm39) |
missense |
probably benign |
0.02 |
R9371:Zfp292
|
UTSW |
4 |
34,810,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R9492:Zfp292
|
UTSW |
4 |
34,810,794 (GRCm39) |
missense |
probably benign |
0.12 |
R9574:Zfp292
|
UTSW |
4 |
34,839,460 (GRCm39) |
missense |
probably damaging |
1.00 |
V7580:Zfp292
|
UTSW |
4 |
34,806,783 (GRCm39) |
missense |
possibly damaging |
0.85 |
V7581:Zfp292
|
UTSW |
4 |
34,806,783 (GRCm39) |
missense |
possibly damaging |
0.85 |
V7582:Zfp292
|
UTSW |
4 |
34,806,783 (GRCm39) |
missense |
possibly damaging |
0.85 |
V7583:Zfp292
|
UTSW |
4 |
34,806,783 (GRCm39) |
missense |
possibly damaging |
0.85 |
Z1177:Zfp292
|
UTSW |
4 |
34,811,058 (GRCm39) |
missense |
probably damaging |
1.00 |
|