Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921504E06Rik |
T |
C |
2: 19,485,401 (GRCm39) |
E422G |
probably damaging |
Het |
Ace3 |
A |
G |
11: 105,888,040 (GRCm39) |
Y287C |
probably damaging |
Het |
Adam34l |
A |
T |
8: 44,079,387 (GRCm39) |
F279Y |
probably damaging |
Het |
Albfm1 |
T |
A |
5: 90,740,727 (GRCm39) |
|
probably null |
Het |
Arfgap3 |
C |
T |
15: 83,187,330 (GRCm39) |
A510T |
probably damaging |
Het |
Atg12 |
A |
G |
18: 46,870,491 (GRCm39) |
F92L |
probably benign |
Het |
Axl |
A |
G |
7: 25,463,336 (GRCm39) |
|
probably benign |
Het |
Chgb |
C |
A |
2: 132,635,847 (GRCm39) |
D596E |
possibly damaging |
Het |
Cmtr2 |
T |
A |
8: 110,947,849 (GRCm39) |
F53Y |
possibly damaging |
Het |
Cnot10 |
A |
G |
9: 114,452,015 (GRCm39) |
F254L |
possibly damaging |
Het |
Crb2 |
G |
T |
2: 37,676,855 (GRCm39) |
C251F |
probably damaging |
Het |
Crybg3 |
A |
T |
16: 59,376,120 (GRCm39) |
|
probably benign |
Het |
Cytl1 |
A |
G |
5: 37,892,940 (GRCm39) |
I17V |
unknown |
Het |
D930020B18Rik |
A |
G |
10: 121,492,123 (GRCm39) |
|
probably benign |
Het |
Depp1 |
A |
G |
6: 116,629,029 (GRCm39) |
N124S |
possibly damaging |
Het |
Dnah11 |
A |
G |
12: 118,009,413 (GRCm39) |
M2083T |
probably benign |
Het |
Dst |
A |
G |
1: 34,231,350 (GRCm39) |
E2656G |
probably benign |
Het |
Dst |
T |
C |
1: 34,267,542 (GRCm39) |
F4995L |
probably damaging |
Het |
Egf |
C |
T |
3: 129,529,618 (GRCm39) |
R264Q |
probably benign |
Het |
Eps15l1 |
A |
G |
8: 73,134,128 (GRCm39) |
I482T |
probably damaging |
Het |
Eqtn |
A |
G |
4: 94,808,199 (GRCm39) |
I201T |
possibly damaging |
Het |
Ero1a |
A |
T |
14: 45,529,893 (GRCm39) |
|
probably null |
Het |
Fcho1 |
T |
C |
8: 72,163,013 (GRCm39) |
H672R |
probably damaging |
Het |
Glt6d1 |
T |
C |
2: 25,684,139 (GRCm39) |
D289G |
probably damaging |
Het |
Gm5134 |
T |
A |
10: 75,844,365 (GRCm39) |
W574R |
probably damaging |
Het |
Gm5414 |
T |
C |
15: 101,533,988 (GRCm39) |
N332D |
probably benign |
Het |
Gnb3 |
T |
A |
6: 124,813,942 (GRCm39) |
E215D |
probably benign |
Het |
Ighv1-30 |
C |
T |
12: 114,781,021 (GRCm39) |
|
noncoding transcript |
Het |
Ighv1-4 |
A |
G |
12: 114,451,147 (GRCm39) |
S15P |
possibly damaging |
Het |
Igkv1-133 |
T |
G |
6: 67,702,505 (GRCm39) |
Y74* |
probably null |
Het |
Il17f |
G |
A |
1: 20,847,987 (GRCm39) |
|
probably benign |
Het |
Itpr2 |
C |
T |
6: 146,274,742 (GRCm39) |
|
probably null |
Het |
Krtap31-1 |
T |
C |
11: 99,799,058 (GRCm39) |
I87T |
possibly damaging |
Het |
Lilra6 |
A |
T |
7: 3,917,889 (GRCm39) |
F85Y |
probably benign |
Het |
Lrig3 |
C |
T |
10: 125,849,277 (GRCm39) |
T999I |
probably benign |
Het |
Myh7b |
T |
C |
2: 155,460,678 (GRCm39) |
I277T |
probably damaging |
Het |
Myo3b |
T |
C |
2: 70,119,808 (GRCm39) |
F984S |
probably damaging |
Het |
Naip5 |
G |
A |
13: 100,382,572 (GRCm39) |
R46W |
probably damaging |
Het |
Nup205 |
T |
A |
6: 35,168,975 (GRCm39) |
|
probably null |
Het |
Or52e18 |
A |
T |
7: 104,609,923 (GRCm39) |
N5K |
probably damaging |
Het |
Pde11a |
C |
T |
2: 76,168,242 (GRCm39) |
R237H |
probably damaging |
Het |
Pdk4 |
T |
C |
6: 5,491,865 (GRCm39) |
N69S |
probably benign |
Het |
Pot1a |
T |
C |
6: 25,752,356 (GRCm39) |
|
probably null |
Het |
Pramel33 |
A |
T |
5: 93,633,057 (GRCm39) |
M50K |
probably damaging |
Het |
Psg23 |
A |
T |
7: 18,341,043 (GRCm39) |
S404T |
possibly damaging |
Het |
Rev1 |
T |
G |
1: 38,093,319 (GRCm39) |
K1075T |
possibly damaging |
Het |
Rrbp1 |
T |
G |
2: 143,805,030 (GRCm39) |
Q1045P |
probably benign |
Het |
Scg2 |
A |
C |
1: 79,414,574 (GRCm39) |
F50V |
probably damaging |
Het |
Sel1l3 |
A |
G |
5: 53,311,629 (GRCm39) |
Y619H |
probably damaging |
Het |
Slco1a5 |
A |
T |
6: 142,213,950 (GRCm39) |
I57K |
possibly damaging |
Het |
Srp72 |
C |
A |
5: 77,146,098 (GRCm39) |
T633K |
probably benign |
Het |
Swt1 |
A |
G |
1: 151,270,520 (GRCm39) |
V565A |
probably benign |
Het |
Tesk1 |
A |
G |
4: 43,443,606 (GRCm39) |
I58V |
possibly damaging |
Het |
Tm2d3 |
T |
A |
7: 65,347,498 (GRCm39) |
L49* |
probably null |
Het |
Tmprss11e |
T |
C |
5: 86,863,502 (GRCm39) |
T188A |
possibly damaging |
Het |
Tnxb |
A |
G |
17: 34,890,845 (GRCm39) |
N396S |
probably benign |
Het |
Tuba8 |
T |
A |
6: 121,199,756 (GRCm39) |
S147T |
probably damaging |
Het |
Usp8 |
A |
G |
2: 126,594,290 (GRCm39) |
D822G |
probably damaging |
Het |
Vmn2r13 |
T |
A |
5: 109,304,566 (GRCm39) |
I622F |
probably damaging |
Het |
Vmn2r24 |
A |
T |
6: 123,764,374 (GRCm39) |
H417L |
possibly damaging |
Het |
Zfp608 |
A |
T |
18: 55,031,180 (GRCm39) |
V920E |
probably damaging |
Het |
Zmym2 |
T |
C |
14: 57,140,461 (GRCm39) |
L100P |
probably damaging |
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 |
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 |
R5635:Etl4
|
UTSW |
2 |
20,811,846 (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 |
|