Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9330159F19Rik |
T |
A |
10: 29,094,273 (GRCm39) |
M53K |
possibly damaging |
Het |
Aldh3b3 |
C |
T |
19: 4,018,512 (GRCm39) |
T409I |
probably benign |
Het |
Ankrd13a |
C |
A |
5: 114,939,778 (GRCm39) |
H468Q |
possibly damaging |
Het |
Ap2a1 |
A |
C |
7: 44,573,325 (GRCm39) |
|
probably benign |
Het |
Arfgef1 |
A |
T |
1: 10,259,085 (GRCm39) |
S671T |
possibly damaging |
Het |
C1ra |
G |
A |
6: 124,493,683 (GRCm39) |
C145Y |
probably damaging |
Het |
Catsperd |
G |
A |
17: 56,939,335 (GRCm39) |
V55M |
possibly damaging |
Het |
Ccdc30 |
T |
C |
4: 119,216,871 (GRCm39) |
N123D |
possibly damaging |
Het |
Cdc20 |
A |
T |
4: 118,293,224 (GRCm39) |
V232E |
possibly damaging |
Het |
Cfap251 |
A |
T |
5: 123,460,635 (GRCm39) |
Q225L |
probably benign |
Het |
Cfap58 |
T |
A |
19: 47,971,981 (GRCm39) |
V637E |
possibly damaging |
Het |
Coq4 |
T |
A |
2: 29,678,367 (GRCm39) |
V24E |
possibly damaging |
Het |
Crim1 |
T |
A |
17: 78,623,070 (GRCm39) |
F423I |
probably damaging |
Het |
Crls1 |
T |
C |
2: 132,706,062 (GRCm39) |
V262A |
possibly damaging |
Het |
Crybb1 |
T |
C |
5: 112,405,425 (GRCm39) |
|
probably null |
Het |
Cutc |
T |
A |
19: 43,744,069 (GRCm39) |
N23K |
probably benign |
Het |
Cxcl10 |
T |
A |
5: 92,495,698 (GRCm39) |
I82F |
probably damaging |
Het |
Cyp3a44 |
A |
T |
5: 145,738,124 (GRCm39) |
F60L |
possibly damaging |
Het |
Dhx9 |
A |
G |
1: 153,359,493 (GRCm39) |
M35T |
probably benign |
Het |
Dnah8 |
A |
G |
17: 30,925,360 (GRCm39) |
E1265G |
probably benign |
Het |
Dzank1 |
C |
G |
2: 144,325,327 (GRCm39) |
D548H |
probably damaging |
Het |
Eef2kmt |
A |
G |
16: 5,066,893 (GRCm39) |
V120A |
probably damaging |
Het |
Elp4 |
A |
G |
2: 105,644,609 (GRCm39) |
|
probably null |
Het |
Exoc6b |
A |
T |
6: 84,828,909 (GRCm39) |
F492I |
probably damaging |
Het |
F2rl2 |
A |
T |
13: 95,837,290 (GRCm39) |
I112F |
possibly damaging |
Het |
Farp1 |
T |
A |
14: 121,513,716 (GRCm39) |
I837N |
possibly damaging |
Het |
Fars2 |
A |
G |
13: 36,594,129 (GRCm39) |
E378G |
probably damaging |
Het |
Fgg |
A |
G |
3: 82,918,730 (GRCm39) |
T248A |
probably benign |
Het |
Flrt3 |
T |
A |
2: 140,502,420 (GRCm39) |
T403S |
probably damaging |
Het |
Fndc3b |
C |
T |
3: 27,596,080 (GRCm39) |
E170K |
probably damaging |
Het |
Gm17728 |
A |
G |
17: 9,641,202 (GRCm39) |
H104R |
probably benign |
Het |
H2ac21 |
C |
A |
3: 96,127,593 (GRCm39) |
T121K |
possibly damaging |
Het |
Hivep1 |
A |
G |
13: 42,313,603 (GRCm39) |
T1948A |
probably benign |
Het |
Hspa4l |
T |
A |
3: 40,700,177 (GRCm39) |
I23N |
probably damaging |
Het |
Ighv1-75 |
A |
G |
12: 115,797,829 (GRCm39) |
V31A |
probably benign |
Het |
Kalrn |
T |
A |
16: 33,834,454 (GRCm39) |
N627I |
probably damaging |
Het |
Lrp1b |
T |
G |
2: 42,542,834 (GRCm39) |
|
probably benign |
Het |
Lrrc36 |
G |
A |
8: 106,184,205 (GRCm39) |
V480M |
probably damaging |
Het |
Map4k3 |
A |
T |
17: 80,920,924 (GRCm39) |
N534K |
possibly damaging |
Het |
Mybpc3 |
C |
T |
2: 90,965,174 (GRCm39) |
T1081I |
probably benign |
Het |
Nfrkb |
T |
C |
9: 31,310,594 (GRCm39) |
S351P |
probably damaging |
Het |
Nme4 |
A |
T |
17: 26,313,205 (GRCm39) |
V43E |
probably damaging |
Het |
Notch1 |
C |
T |
2: 26,366,173 (GRCm39) |
E794K |
probably damaging |
Het |
Nufip1 |
A |
T |
14: 76,363,586 (GRCm39) |
K270M |
probably damaging |
Het |
Or10ak16 |
G |
T |
4: 118,750,832 (GRCm39) |
G184V |
probably benign |
Het |
Or1e30 |
G |
T |
11: 73,678,460 (GRCm39) |
R232L |
probably benign |
Het |
Or51b6 |
G |
A |
7: 103,555,845 (GRCm39) |
M66I |
probably benign |
Het |
Or5t5 |
A |
G |
2: 86,616,070 (GRCm39) |
|
probably null |
Het |
Or8g51 |
A |
G |
9: 38,609,455 (GRCm39) |
I73T |
possibly damaging |
Het |
Pcdhb15 |
T |
A |
18: 37,606,823 (GRCm39) |
Y18* |
probably null |
Het |
Pcdhb21 |
A |
T |
18: 37,646,970 (GRCm39) |
Y33F |
probably benign |
Het |
Pds5b |
T |
A |
5: 150,701,686 (GRCm39) |
H772Q |
possibly damaging |
Het |
Pik3r4 |
C |
A |
9: 105,545,024 (GRCm39) |
H168N |
probably benign |
Het |
Pitpnm3 |
A |
G |
11: 71,957,986 (GRCm39) |
S386P |
possibly damaging |
Het |
Plg |
A |
G |
17: 12,614,641 (GRCm39) |
H307R |
probably damaging |
Het |
Prdm9 |
A |
C |
17: 15,782,702 (GRCm39) |
D96E |
probably damaging |
Het |
Prmt8 |
A |
G |
6: 127,745,692 (GRCm39) |
S7P |
probably damaging |
Het |
Prune2 |
T |
C |
19: 17,095,573 (GRCm39) |
V359A |
probably benign |
Het |
Pxn |
A |
T |
5: 115,689,551 (GRCm39) |
Q279L |
probably benign |
Het |
Rarb |
A |
T |
14: 16,443,788 (GRCm38) |
C167S |
probably damaging |
Het |
Rps6kb2 |
T |
A |
19: 4,211,133 (GRCm39) |
I131F |
probably damaging |
Het |
Sec14l3 |
T |
A |
11: 4,021,484 (GRCm39) |
V219E |
probably damaging |
Het |
Simc1 |
A |
G |
13: 54,673,217 (GRCm39) |
T522A |
probably benign |
Het |
Slc1a6 |
T |
C |
10: 78,624,925 (GRCm39) |
V110A |
possibly damaging |
Het |
Slc38a11 |
T |
G |
2: 65,191,747 (GRCm39) |
|
probably null |
Het |
Snx13 |
T |
A |
12: 35,190,170 (GRCm39) |
D840E |
probably benign |
Het |
Sp100 |
C |
A |
1: 85,609,985 (GRCm39) |
|
probably benign |
Het |
Spc24 |
G |
T |
9: 21,668,686 (GRCm39) |
L104I |
probably damaging |
Het |
Surf4 |
T |
C |
2: 26,823,325 (GRCm39) |
N4D |
probably benign |
Het |
Tas2r131 |
A |
T |
6: 132,934,571 (GRCm39) |
D79E |
probably benign |
Het |
Tbc1d20 |
T |
C |
2: 152,153,381 (GRCm39) |
S304P |
probably benign |
Het |
Tbrg1 |
T |
C |
9: 37,566,287 (GRCm39) |
|
probably benign |
Het |
Tmem214 |
A |
G |
5: 31,028,861 (GRCm39) |
N150S |
probably damaging |
Het |
Trappc13 |
A |
T |
13: 104,286,606 (GRCm39) |
I217K |
probably benign |
Het |
Ttc41 |
T |
A |
10: 86,572,841 (GRCm39) |
C738S |
probably benign |
Het |
Ttn |
T |
C |
2: 76,540,068 (GRCm39) |
Q25979R |
probably benign |
Het |
Tubb2b |
A |
T |
13: 34,312,180 (GRCm39) |
N204K |
probably damaging |
Het |
Ube3a |
T |
A |
7: 58,938,236 (GRCm39) |
M713K |
probably damaging |
Het |
Usp37 |
T |
C |
1: 74,534,970 (GRCm39) |
|
probably benign |
Het |
Vegfb |
T |
A |
19: 6,960,214 (GRCm39) |
*189C |
probably null |
Het |
Vmn2r82 |
A |
G |
10: 79,214,652 (GRCm39) |
N212D |
probably benign |
Het |
Vta1 |
A |
T |
10: 14,543,866 (GRCm39) |
|
probably null |
Het |
Xdh |
T |
G |
17: 74,220,870 (GRCm39) |
I620L |
possibly damaging |
Het |
Xpnpep3 |
A |
G |
15: 81,320,970 (GRCm39) |
Y283C |
probably benign |
Het |
Zscan18 |
A |
G |
7: 12,504,791 (GRCm39) |
S609P |
probably benign |
Het |
|
Other mutations in Etl4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00907:Etl4
|
APN |
2 |
20,771,289 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL00944:Etl4
|
APN |
2 |
20,534,865 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL01078:Etl4
|
APN |
2 |
20,811,342 (GRCm39) |
nonsense |
probably null |
|
IGL01099:Etl4
|
APN |
2 |
20,811,922 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01337:Etl4
|
APN |
2 |
20,790,198 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01348:Etl4
|
APN |
2 |
20,811,784 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01349:Etl4
|
APN |
2 |
20,718,207 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01407:Etl4
|
APN |
2 |
20,748,667 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01552:Etl4
|
APN |
2 |
20,783,000 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01662:Etl4
|
APN |
2 |
20,811,460 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01687:Etl4
|
APN |
2 |
20,534,898 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01793:Etl4
|
APN |
2 |
20,748,709 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01844:Etl4
|
APN |
2 |
20,811,493 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02025:Etl4
|
APN |
2 |
20,811,337 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02088:Etl4
|
APN |
2 |
20,811,359 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02134:Etl4
|
APN |
2 |
20,811,240 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02369:Etl4
|
APN |
2 |
20,535,000 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02480:Etl4
|
APN |
2 |
20,793,335 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02560:Etl4
|
APN |
2 |
20,748,529 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02851:Etl4
|
APN |
2 |
20,812,840 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL02893:Etl4
|
APN |
2 |
20,765,021 (GRCm39) |
splice site |
probably benign |
|
IGL02951:Etl4
|
APN |
2 |
20,806,348 (GRCm39) |
splice site |
probably benign |
|
IGL03119:Etl4
|
APN |
2 |
20,718,198 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03267:Etl4
|
APN |
2 |
20,789,993 (GRCm39) |
nonsense |
probably null |
|
IGL03379:Etl4
|
APN |
2 |
20,666,827 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0038:Etl4
|
UTSW |
2 |
20,748,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R0038:Etl4
|
UTSW |
2 |
20,748,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R0095:Etl4
|
UTSW |
2 |
20,748,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R0100:Etl4
|
UTSW |
2 |
20,344,716 (GRCm39) |
missense |
probably benign |
|
R0311:Etl4
|
UTSW |
2 |
20,811,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R0346:Etl4
|
UTSW |
2 |
20,764,463 (GRCm39) |
critical splice donor site |
probably null |
|
R0348:Etl4
|
UTSW |
2 |
20,782,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R0379:Etl4
|
UTSW |
2 |
20,812,165 (GRCm39) |
missense |
probably damaging |
0.98 |
R0571:Etl4
|
UTSW |
2 |
20,748,580 (GRCm39) |
missense |
probably damaging |
0.99 |
R0697:Etl4
|
UTSW |
2 |
20,748,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R0707:Etl4
|
UTSW |
2 |
20,810,382 (GRCm39) |
splice site |
probably benign |
|
R0980:Etl4
|
UTSW |
2 |
20,806,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R1120:Etl4
|
UTSW |
2 |
20,811,514 (GRCm39) |
missense |
probably benign |
0.00 |
R1254:Etl4
|
UTSW |
2 |
20,812,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R1346:Etl4
|
UTSW |
2 |
20,810,955 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1460:Etl4
|
UTSW |
2 |
20,793,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R1503:Etl4
|
UTSW |
2 |
20,748,685 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1547:Etl4
|
UTSW |
2 |
20,790,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R1627:Etl4
|
UTSW |
2 |
20,806,390 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1635:Etl4
|
UTSW |
2 |
20,811,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R1716:Etl4
|
UTSW |
2 |
20,748,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R1795:Etl4
|
UTSW |
2 |
20,812,837 (GRCm39) |
critical splice donor site |
probably null |
|
R1885:Etl4
|
UTSW |
2 |
20,748,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R2039:Etl4
|
UTSW |
2 |
20,790,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R2083:Etl4
|
UTSW |
2 |
20,748,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R2109:Etl4
|
UTSW |
2 |
20,790,153 (GRCm39) |
missense |
probably benign |
0.27 |
R2153:Etl4
|
UTSW |
2 |
20,803,545 (GRCm39) |
missense |
probably benign |
0.00 |
R2403:Etl4
|
UTSW |
2 |
20,812,117 (GRCm39) |
nonsense |
probably null |
|
R2883:Etl4
|
UTSW |
2 |
20,810,985 (GRCm39) |
missense |
possibly damaging |
0.83 |
R2985:Etl4
|
UTSW |
2 |
20,786,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R3402:Etl4
|
UTSW |
2 |
20,786,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R3696:Etl4
|
UTSW |
2 |
20,806,473 (GRCm39) |
critical splice donor site |
probably null |
|
R3755:Etl4
|
UTSW |
2 |
20,748,348 (GRCm39) |
missense |
probably benign |
0.10 |
R3813:Etl4
|
UTSW |
2 |
20,793,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R3829:Etl4
|
UTSW |
2 |
20,790,232 (GRCm39) |
missense |
probably benign |
0.07 |
R3887:Etl4
|
UTSW |
2 |
20,534,772 (GRCm39) |
nonsense |
probably null |
|
R3888:Etl4
|
UTSW |
2 |
20,534,772 (GRCm39) |
nonsense |
probably null |
|
R3889:Etl4
|
UTSW |
2 |
20,534,772 (GRCm39) |
nonsense |
probably null |
|
R3958:Etl4
|
UTSW |
2 |
20,344,854 (GRCm39) |
missense |
probably benign |
|
R3959:Etl4
|
UTSW |
2 |
20,344,854 (GRCm39) |
missense |
probably benign |
|
R3960:Etl4
|
UTSW |
2 |
20,344,854 (GRCm39) |
missense |
probably benign |
|
R4058:Etl4
|
UTSW |
2 |
20,810,830 (GRCm39) |
missense |
possibly damaging |
0.59 |
R4074:Etl4
|
UTSW |
2 |
20,814,030 (GRCm39) |
utr 3 prime |
probably benign |
|
R4077:Etl4
|
UTSW |
2 |
20,812,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R4078:Etl4
|
UTSW |
2 |
20,812,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R4127:Etl4
|
UTSW |
2 |
20,748,886 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4200:Etl4
|
UTSW |
2 |
20,786,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R4492:Etl4
|
UTSW |
2 |
20,811,676 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4514:Etl4
|
UTSW |
2 |
20,666,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R4820:Etl4
|
UTSW |
2 |
20,811,496 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4825:Etl4
|
UTSW |
2 |
20,811,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R4888:Etl4
|
UTSW |
2 |
20,344,922 (GRCm39) |
critical splice donor site |
probably null |
|
R4938:Etl4
|
UTSW |
2 |
20,803,460 (GRCm39) |
missense |
probably benign |
0.00 |
R4943:Etl4
|
UTSW |
2 |
20,812,092 (GRCm39) |
missense |
probably benign |
0.05 |
R5121:Etl4
|
UTSW |
2 |
20,344,922 (GRCm39) |
critical splice donor site |
probably null |
|
R5191:Etl4
|
UTSW |
2 |
20,344,810 (GRCm39) |
missense |
probably damaging |
0.99 |
R5198:Etl4
|
UTSW |
2 |
20,718,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R5199:Etl4
|
UTSW |
2 |
20,748,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R5470:Etl4
|
UTSW |
2 |
20,534,791 (GRCm39) |
missense |
probably damaging |
0.99 |
R5513:Etl4
|
UTSW |
2 |
20,748,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R5620:Etl4
|
UTSW |
2 |
20,535,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R5641:Etl4
|
UTSW |
2 |
20,811,273 (GRCm39) |
frame shift |
probably null |
|
R5690:Etl4
|
UTSW |
2 |
20,810,647 (GRCm39) |
missense |
probably benign |
0.01 |
R5784:Etl4
|
UTSW |
2 |
20,811,016 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5794:Etl4
|
UTSW |
2 |
20,811,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R5908:Etl4
|
UTSW |
2 |
20,748,718 (GRCm39) |
missense |
probably damaging |
0.96 |
R5982:Etl4
|
UTSW |
2 |
20,785,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R6151:Etl4
|
UTSW |
2 |
20,718,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R6192:Etl4
|
UTSW |
2 |
20,806,362 (GRCm39) |
missense |
probably damaging |
0.98 |
R6238:Etl4
|
UTSW |
2 |
20,806,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R6248:Etl4
|
UTSW |
2 |
20,813,900 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6292:Etl4
|
UTSW |
2 |
20,748,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R6610:Etl4
|
UTSW |
2 |
20,718,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R6739:Etl4
|
UTSW |
2 |
20,718,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R6846:Etl4
|
UTSW |
2 |
20,748,919 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6863:Etl4
|
UTSW |
2 |
20,811,120 (GRCm39) |
missense |
probably benign |
0.01 |
R6873:Etl4
|
UTSW |
2 |
20,802,803 (GRCm39) |
splice site |
probably null |
|
R7003:Etl4
|
UTSW |
2 |
20,810,695 (GRCm39) |
missense |
probably benign |
0.03 |
R7155:Etl4
|
UTSW |
2 |
20,811,742 (GRCm39) |
missense |
probably damaging |
0.96 |
R7207:Etl4
|
UTSW |
2 |
20,714,387 (GRCm39) |
missense |
probably damaging |
0.99 |
R7230:Etl4
|
UTSW |
2 |
20,802,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R7305:Etl4
|
UTSW |
2 |
20,714,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R7389:Etl4
|
UTSW |
2 |
20,789,904 (GRCm39) |
nonsense |
probably null |
|
R7396:Etl4
|
UTSW |
2 |
20,803,449 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7441:Etl4
|
UTSW |
2 |
20,749,000 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7626:Etl4
|
UTSW |
2 |
20,718,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R7776:Etl4
|
UTSW |
2 |
20,811,957 (GRCm39) |
missense |
probably damaging |
0.99 |
R7779:Etl4
|
UTSW |
2 |
20,714,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R7798:Etl4
|
UTSW |
2 |
20,786,757 (GRCm39) |
critical splice donor site |
probably null |
|
R7851:Etl4
|
UTSW |
2 |
20,748,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R7861:Etl4
|
UTSW |
2 |
20,810,721 (GRCm39) |
missense |
probably benign |
|
R7901:Etl4
|
UTSW |
2 |
20,294,821 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8053:Etl4
|
UTSW |
2 |
20,666,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R8124:Etl4
|
UTSW |
2 |
20,811,451 (GRCm39) |
missense |
probably benign |
0.06 |
R8133:Etl4
|
UTSW |
2 |
20,811,082 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8203:Etl4
|
UTSW |
2 |
20,789,916 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8238:Etl4
|
UTSW |
2 |
20,811,342 (GRCm39) |
nonsense |
probably null |
|
R8263:Etl4
|
UTSW |
2 |
20,748,965 (GRCm39) |
missense |
probably benign |
0.00 |
R8299:Etl4
|
UTSW |
2 |
20,748,874 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8318:Etl4
|
UTSW |
2 |
20,793,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R8334:Etl4
|
UTSW |
2 |
20,785,857 (GRCm39) |
missense |
probably damaging |
0.96 |
R8443:Etl4
|
UTSW |
2 |
20,810,977 (GRCm39) |
missense |
probably benign |
0.04 |
R8525:Etl4
|
UTSW |
2 |
20,534,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R8679:Etl4
|
UTSW |
2 |
20,714,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R8918:Etl4
|
UTSW |
2 |
20,811,246 (GRCm39) |
missense |
probably benign |
0.00 |
R8918:Etl4
|
UTSW |
2 |
20,748,733 (GRCm39) |
missense |
probably benign |
|
R9062:Etl4
|
UTSW |
2 |
20,748,616 (GRCm39) |
missense |
probably damaging |
0.99 |
R9095:Etl4
|
UTSW |
2 |
20,782,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R9200:Etl4
|
UTSW |
2 |
20,786,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R9416:Etl4
|
UTSW |
2 |
20,748,784 (GRCm39) |
missense |
probably benign |
0.17 |
R9437:Etl4
|
UTSW |
2 |
20,813,872 (GRCm39) |
missense |
probably benign |
0.20 |
R9451:Etl4
|
UTSW |
2 |
20,813,926 (GRCm39) |
missense |
probably benign |
0.03 |
R9489:Etl4
|
UTSW |
2 |
20,771,345 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9531:Etl4
|
UTSW |
2 |
20,294,818 (GRCm39) |
start codon destroyed |
probably null |
0.01 |
R9605:Etl4
|
UTSW |
2 |
20,771,345 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9623:Etl4
|
UTSW |
2 |
20,811,052 (GRCm39) |
missense |
|
|
R9631:Etl4
|
UTSW |
2 |
20,666,749 (GRCm39) |
missense |
probably benign |
0.28 |
R9632:Etl4
|
UTSW |
2 |
20,666,749 (GRCm39) |
missense |
probably benign |
0.28 |
R9646:Etl4
|
UTSW |
2 |
20,802,724 (GRCm39) |
missense |
probably benign |
0.00 |
R9732:Etl4
|
UTSW |
2 |
20,748,373 (GRCm39) |
missense |
probably damaging |
0.98 |
R9755:Etl4
|
UTSW |
2 |
20,790,048 (GRCm39) |
missense |
probably benign |
0.17 |
R9771:Etl4
|
UTSW |
2 |
20,811,537 (GRCm39) |
missense |
probably benign |
|
RF003:Etl4
|
UTSW |
2 |
20,524,729 (GRCm39) |
nonsense |
probably null |
|
X0018:Etl4
|
UTSW |
2 |
20,814,001 (GRCm39) |
missense |
probably damaging |
0.98 |
X0022:Etl4
|
UTSW |
2 |
20,714,375 (GRCm39) |
missense |
probably damaging |
1.00 |
|