Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3110009E18Rik |
A |
G |
1: 120,099,216 (GRCm39) |
|
probably null |
Het |
4930550C14Rik |
G |
T |
9: 53,325,683 (GRCm39) |
R73S |
probably damaging |
Het |
Abca1 |
A |
G |
4: 53,085,261 (GRCm39) |
V517A |
probably benign |
Het |
Adck5 |
A |
T |
15: 76,478,887 (GRCm39) |
K370N |
possibly damaging |
Het |
Akap6 |
A |
C |
12: 53,072,575 (GRCm39) |
D981A |
probably damaging |
Het |
Apbb1 |
G |
A |
7: 105,223,459 (GRCm39) |
R51* |
probably null |
Het |
Arhgap23 |
A |
G |
11: 97,391,238 (GRCm39) |
M1252V |
probably benign |
Het |
Arhgef1 |
A |
G |
7: 24,617,367 (GRCm39) |
T354A |
probably benign |
Het |
Arid1a |
G |
T |
4: 133,412,287 (GRCm39) |
Q1636K |
unknown |
Het |
Asmt |
C |
T |
X: 169,110,202 (GRCm39) |
A237V |
possibly damaging |
Het |
Brat1 |
T |
A |
5: 140,691,716 (GRCm39) |
C43S |
probably benign |
Het |
Cd36 |
T |
C |
5: 18,000,593 (GRCm39) |
Y370C |
probably damaging |
Het |
Ceacam12 |
A |
T |
7: 17,803,030 (GRCm39) |
L145F |
probably benign |
Het |
Col24a1 |
C |
T |
3: 145,019,815 (GRCm39) |
T62I |
probably damaging |
Het |
Col6a3 |
G |
T |
1: 90,741,475 (GRCm39) |
N652K |
possibly damaging |
Het |
Dcbld1 |
T |
C |
10: 52,180,756 (GRCm39) |
L140P |
probably damaging |
Het |
Dhrs13 |
G |
A |
11: 77,927,808 (GRCm39) |
C218Y |
probably damaging |
Het |
Diaph1 |
T |
G |
18: 37,986,406 (GRCm39) |
E1158A |
probably damaging |
Het |
Emp2 |
A |
C |
16: 10,110,145 (GRCm39) |
F20C |
probably damaging |
Het |
Enpep |
T |
C |
3: 129,126,067 (GRCm39) |
I22V |
possibly damaging |
Het |
Epha2 |
A |
G |
4: 141,045,791 (GRCm39) |
|
probably null |
Het |
Eprs1 |
G |
T |
1: 185,139,951 (GRCm39) |
|
probably null |
Het |
Exoc3l2 |
C |
A |
7: 19,225,670 (GRCm39) |
S89* |
probably null |
Het |
F5 |
G |
A |
1: 164,017,756 (GRCm39) |
C611Y |
probably damaging |
Het |
F5 |
A |
T |
1: 164,009,204 (GRCm39) |
I325F |
probably damaging |
Het |
Fam133b |
A |
T |
5: 3,609,133 (GRCm39) |
S116C |
probably null |
Het |
Fam13b |
A |
T |
18: 34,627,330 (GRCm39) |
D190E |
probably damaging |
Het |
Fam169a |
T |
G |
13: 97,230,138 (GRCm39) |
Y58D |
probably damaging |
Het |
Far1 |
G |
A |
7: 113,160,603 (GRCm39) |
R383H |
possibly damaging |
Het |
Fnbp1l |
T |
C |
3: 122,364,579 (GRCm39) |
K52R |
possibly damaging |
Het |
Foxj3 |
C |
A |
4: 119,480,468 (GRCm39) |
Q469K |
unknown |
Het |
Frs3 |
A |
T |
17: 48,000,013 (GRCm39) |
|
probably benign |
Het |
Gdpd3 |
A |
G |
7: 126,374,674 (GRCm39) |
S290G |
probably benign |
Het |
Gmip |
T |
A |
8: 70,269,735 (GRCm39) |
L610Q |
probably damaging |
Het |
Gprc5c |
T |
A |
11: 114,754,851 (GRCm39) |
I176N |
probably damaging |
Het |
Grm3 |
A |
G |
5: 9,561,556 (GRCm39) |
F765L |
probably damaging |
Het |
Hhat |
A |
T |
1: 192,442,065 (GRCm39) |
L2Q |
probably damaging |
Het |
Hspbap1 |
T |
C |
16: 35,637,592 (GRCm39) |
S214P |
probably damaging |
Het |
Ighv1-62-3 |
C |
A |
12: 115,424,909 (GRCm39) |
V21F |
probably damaging |
Het |
Kcnj15 |
A |
T |
16: 95,096,527 (GRCm39) |
K50* |
probably null |
Het |
Kidins220 |
T |
C |
12: 25,106,908 (GRCm39) |
S1454P |
possibly damaging |
Het |
Kl |
T |
A |
5: 150,912,318 (GRCm39) |
M689K |
possibly damaging |
Het |
Klhl23 |
T |
G |
2: 69,655,198 (GRCm39) |
L356R |
probably damaging |
Het |
Kndc1 |
A |
T |
7: 139,501,129 (GRCm39) |
D806V |
probably benign |
Het |
Krt26 |
T |
C |
11: 99,228,315 (GRCm39) |
E139G |
probably benign |
Het |
Lefty1 |
T |
C |
1: 180,762,681 (GRCm39) |
F3L |
unknown |
Het |
Madd |
A |
C |
2: 90,995,802 (GRCm39) |
Y853* |
probably null |
Het |
Map1a |
T |
A |
2: 121,120,304 (GRCm39) |
D63E |
probably benign |
Het |
Mdn1 |
T |
A |
4: 32,684,735 (GRCm39) |
V815E |
probably damaging |
Het |
Mettl3 |
A |
G |
14: 52,532,477 (GRCm39) |
Y569H |
probably damaging |
Het |
Mknk2 |
T |
C |
10: 80,504,859 (GRCm39) |
|
probably null |
Het |
Mpp3 |
C |
A |
11: 101,899,392 (GRCm39) |
R376S |
probably benign |
Het |
Ncoa4-ps |
T |
G |
12: 119,224,841 (GRCm39) |
|
noncoding transcript |
Het |
Nup160 |
T |
A |
2: 90,520,449 (GRCm39) |
Y293* |
probably null |
Het |
Nup58 |
A |
T |
14: 60,482,065 (GRCm39) |
F100I |
possibly damaging |
Het |
Nxpe2 |
A |
C |
9: 48,237,491 (GRCm39) |
L255V |
probably benign |
Het |
Or10ab4 |
A |
G |
7: 107,655,106 (GRCm39) |
I306V |
probably benign |
Het |
Or1e30 |
T |
A |
11: 73,678,521 (GRCm39) |
Y252* |
probably null |
Het |
Or2l5 |
A |
T |
16: 19,334,281 (GRCm39) |
L35Q |
probably damaging |
Het |
Or4d11 |
T |
C |
19: 12,014,100 (GRCm39) |
E2G |
probably benign |
Het |
Padi3 |
A |
T |
4: 140,523,705 (GRCm39) |
D248E |
probably damaging |
Het |
Paxip1 |
G |
T |
5: 27,966,616 (GRCm39) |
H637N |
probably damaging |
Het |
Pde4b |
T |
A |
4: 102,458,748 (GRCm39) |
M296K |
probably damaging |
Het |
Pkd1 |
A |
G |
17: 24,794,580 (GRCm39) |
H2089R |
probably benign |
Het |
Plaat5 |
C |
T |
19: 7,596,656 (GRCm39) |
P148S |
probably damaging |
Het |
Prpf40a |
T |
C |
2: 53,047,927 (GRCm39) |
M197V |
probably benign |
Het |
Rhebl1 |
T |
C |
15: 98,776,160 (GRCm39) |
I165V |
probably benign |
Het |
Rock1 |
A |
T |
18: 10,106,426 (GRCm39) |
V481E |
possibly damaging |
Het |
Rtca |
T |
A |
3: 116,301,476 (GRCm39) |
T24S |
probably benign |
Het |
Serpina3c |
T |
A |
12: 104,118,327 (GRCm39) |
I4F |
possibly damaging |
Het |
Serpina3j |
C |
A |
12: 104,283,649 (GRCm39) |
A249E |
possibly damaging |
Het |
Slc38a9 |
A |
G |
13: 112,825,910 (GRCm39) |
N116S |
probably damaging |
Het |
Slco2b1 |
C |
T |
7: 99,339,770 (GRCm39) |
V58I |
possibly damaging |
Het |
Slfn8 |
T |
A |
11: 82,908,147 (GRCm39) |
Y132F |
probably damaging |
Het |
Smg6 |
T |
G |
11: 75,047,033 (GRCm39) |
I1242S |
probably damaging |
Het |
Tap2 |
G |
T |
17: 34,431,021 (GRCm39) |
V374L |
probably benign |
Het |
Tbc1d10b |
G |
A |
7: 126,807,168 (GRCm39) |
T123M |
probably damaging |
Het |
Tenm2 |
A |
C |
11: 35,899,610 (GRCm39) |
V2516G |
probably damaging |
Het |
Tenm3 |
C |
T |
8: 48,848,608 (GRCm39) |
R12Q |
probably damaging |
Het |
Tmem130 |
T |
A |
5: 144,674,661 (GRCm39) |
M355L |
probably benign |
Het |
Tns4 |
C |
T |
11: 98,966,376 (GRCm39) |
S433N |
probably benign |
Het |
Traip |
G |
T |
9: 107,847,818 (GRCm39) |
|
probably null |
Het |
Trmo |
G |
A |
4: 46,389,390 (GRCm39) |
R2C |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,774,504 (GRCm39) |
I2134N |
probably damaging |
Het |
Uba1y |
A |
G |
Y: 825,984 (GRCm39) |
D380G |
probably benign |
Het |
Ube2t |
T |
A |
1: 134,895,698 (GRCm39) |
|
probably null |
Het |
Ugdh |
A |
T |
5: 65,574,924 (GRCm39) |
Y367* |
probably null |
Het |
Usp45 |
A |
C |
4: 21,810,797 (GRCm39) |
D331A |
probably damaging |
Het |
Vmn1r84 |
G |
T |
7: 12,095,841 (GRCm39) |
T284K |
possibly damaging |
Het |
Vmn1r91 |
T |
A |
7: 19,835,360 (GRCm39) |
F93Y |
probably benign |
Het |
Vmn2r77 |
T |
A |
7: 86,450,878 (GRCm39) |
Y255N |
probably benign |
Het |
Vmn2r96 |
A |
T |
17: 18,804,221 (GRCm39) |
Q490H |
probably benign |
Het |
Vwa2 |
A |
G |
19: 56,891,897 (GRCm39) |
|
probably null |
Het |
Vwf |
A |
G |
6: 125,634,028 (GRCm39) |
K169E |
unknown |
Het |
Zc3h7b |
G |
C |
15: 81,662,911 (GRCm39) |
|
probably null |
Het |
Zfp458 |
T |
A |
13: 67,405,662 (GRCm39) |
H259L |
possibly damaging |
Het |
Zfp647 |
G |
A |
15: 76,796,285 (GRCm39) |
P125L |
probably damaging |
Het |
Zfp804b |
A |
G |
5: 6,819,910 (GRCm39) |
V1051A |
probably benign |
Het |
Zfp998 |
A |
T |
13: 66,579,740 (GRCm39) |
C248S |
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 |
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 |
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 |
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 |
|