Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
T |
A |
11: 109,844,423 (GRCm39) |
E931D |
possibly damaging |
Het |
Aebp1 |
C |
T |
11: 5,817,911 (GRCm39) |
T62I |
possibly damaging |
Het |
Babam2 |
A |
T |
5: 31,977,964 (GRCm39) |
E139V |
possibly damaging |
Het |
Bclaf1 |
C |
T |
10: 20,198,809 (GRCm39) |
R67* |
probably null |
Het |
Bcr |
C |
A |
10: 75,012,248 (GRCm39) |
T51K |
probably benign |
Het |
Best3 |
T |
A |
10: 116,840,322 (GRCm39) |
C251S |
probably damaging |
Het |
Birc6 |
A |
G |
17: 74,955,153 (GRCm39) |
M3457V |
probably benign |
Het |
C87436 |
C |
A |
6: 86,422,957 (GRCm39) |
T177K |
possibly damaging |
Het |
Cabin1 |
T |
A |
10: 75,561,394 (GRCm39) |
T1036S |
probably benign |
Het |
Catsperg2 |
C |
A |
7: 29,412,442 (GRCm39) |
V383L |
possibly damaging |
Het |
Ccdc182 |
C |
T |
11: 88,185,165 (GRCm39) |
Q82* |
probably null |
Het |
Ccl9 |
T |
C |
11: 83,466,700 (GRCm39) |
T76A |
probably damaging |
Het |
Cdc16 |
G |
T |
8: 13,831,399 (GRCm39) |
C544F |
possibly damaging |
Het |
Cdh18 |
A |
C |
15: 23,474,302 (GRCm39) |
D724A |
possibly damaging |
Het |
Cdip1 |
G |
A |
16: 4,587,946 (GRCm39) |
P6S |
probably damaging |
Het |
Col12a1 |
A |
G |
9: 79,537,842 (GRCm39) |
V2542A |
probably damaging |
Het |
Dnajc13 |
G |
T |
9: 104,061,814 (GRCm39) |
T1380K |
possibly damaging |
Het |
Dsg4 |
T |
A |
18: 20,598,226 (GRCm39) |
S715T |
possibly damaging |
Het |
Dync2h1 |
G |
T |
9: 6,955,986 (GRCm39) |
T4132K |
probably benign |
Het |
Egfem1 |
A |
T |
3: 29,711,419 (GRCm39) |
|
probably null |
Het |
Exoc3l2 |
A |
G |
7: 19,213,957 (GRCm39) |
E461G |
unknown |
Het |
Fam135b |
A |
G |
15: 71,320,518 (GRCm39) |
|
probably null |
Het |
Flrt3 |
G |
T |
2: 140,502,836 (GRCm39) |
P264Q |
possibly damaging |
Het |
Fmn2 |
G |
C |
1: 174,330,019 (GRCm39) |
E136D |
unknown |
Het |
Fosl2 |
A |
G |
5: 32,304,217 (GRCm39) |
I51V |
probably benign |
Het |
Foxm1 |
A |
G |
6: 128,347,998 (GRCm39) |
T307A |
probably damaging |
Het |
Garem1 |
T |
C |
18: 21,281,408 (GRCm39) |
D316G |
possibly damaging |
Het |
Gm14403 |
A |
T |
2: 177,200,345 (GRCm39) |
H97L |
probably damaging |
Het |
Gm5616 |
A |
G |
9: 48,361,890 (GRCm39) |
|
noncoding transcript |
Het |
Hkdc1 |
T |
C |
10: 62,229,589 (GRCm39) |
D696G |
probably benign |
Het |
Igkv1-88 |
C |
A |
6: 68,839,432 (GRCm39) |
W60L |
probably damaging |
Het |
Iqgap3 |
G |
A |
3: 87,998,899 (GRCm39) |
W333* |
probably null |
Het |
Itgb4 |
C |
T |
11: 115,874,983 (GRCm39) |
R447W |
probably benign |
Het |
Kcnk3 |
G |
T |
5: 30,780,014 (GRCm39) |
V355L |
probably benign |
Het |
Kmt5c |
A |
C |
7: 4,749,790 (GRCm39) |
K436T |
probably damaging |
Het |
Lynx1 |
T |
C |
15: 74,623,264 (GRCm39) |
Y56C |
possibly damaging |
Het |
Lypd5 |
T |
C |
7: 24,052,462 (GRCm39) |
S149P |
probably damaging |
Het |
Map3k21 |
A |
T |
8: 126,638,169 (GRCm39) |
N252Y |
probably damaging |
Het |
Mgat2 |
T |
C |
12: 69,232,454 (GRCm39) |
W343R |
probably damaging |
Het |
Misp |
T |
G |
10: 79,663,728 (GRCm39) |
Y567* |
probably null |
Het |
Mrgprb1 |
A |
T |
7: 48,097,568 (GRCm39) |
S115T |
probably benign |
Het |
Muc16 |
A |
C |
9: 18,558,442 (GRCm39) |
I2617R |
unknown |
Het |
Myo19 |
T |
A |
11: 84,790,226 (GRCm39) |
V394E |
probably damaging |
Het |
Myo9b |
T |
A |
8: 71,801,040 (GRCm39) |
L1065Q |
probably benign |
Het |
Nap1l1 |
A |
G |
10: 111,331,229 (GRCm39) |
D405G |
possibly damaging |
Het |
Napb |
A |
T |
2: 148,542,411 (GRCm39) |
|
probably null |
Het |
Nbas |
A |
G |
12: 13,443,431 (GRCm39) |
Y1162C |
probably benign |
Het |
Nfam1 |
A |
T |
15: 82,917,325 (GRCm39) |
L36Q |
probably damaging |
Het |
Nrros |
T |
C |
16: 31,963,411 (GRCm39) |
D202G |
probably damaging |
Het |
Or51k1 |
T |
G |
7: 103,661,117 (GRCm39) |
H264P |
probably damaging |
Het |
Or7a39 |
T |
G |
10: 78,715,787 (GRCm39) |
Y260* |
probably null |
Het |
Osgin2 |
T |
C |
4: 15,998,908 (GRCm39) |
E238G |
probably benign |
Het |
Papss2 |
A |
G |
19: 32,616,636 (GRCm39) |
T221A |
probably benign |
Het |
Pcdhga12 |
A |
C |
18: 37,901,084 (GRCm39) |
K639Q |
probably damaging |
Het |
Pkhd1l1 |
T |
A |
15: 44,352,900 (GRCm39) |
|
probably null |
Het |
Pmepa1 |
A |
G |
2: 173,076,105 (GRCm39) |
S83P |
possibly damaging |
Het |
Pnp |
G |
A |
14: 51,188,000 (GRCm39) |
V118M |
probably damaging |
Het |
Ppat |
T |
C |
5: 77,063,112 (GRCm39) |
T500A |
probably benign |
Het |
Pramel22 |
C |
A |
4: 143,381,034 (GRCm39) |
V330F |
probably damaging |
Het |
Rab11fip4 |
A |
G |
11: 79,581,601 (GRCm39) |
N532S |
probably benign |
Het |
Rbm25 |
A |
G |
12: 83,718,725 (GRCm39) |
D499G |
probably damaging |
Het |
Rnf139 |
A |
G |
15: 58,770,687 (GRCm39) |
I237M |
possibly damaging |
Het |
Rrp15 |
C |
T |
1: 186,471,952 (GRCm39) |
S85N |
possibly damaging |
Het |
Sidt1 |
T |
C |
16: 44,082,071 (GRCm39) |
Y568C |
probably damaging |
Het |
Slirp |
A |
G |
12: 87,490,784 (GRCm39) |
T29A |
probably damaging |
Het |
Sltm |
G |
C |
9: 70,494,086 (GRCm39) |
E828Q |
probably damaging |
Het |
Spindoc |
A |
G |
19: 7,351,960 (GRCm39) |
I129T |
probably damaging |
Het |
Spire1 |
T |
A |
18: 67,630,386 (GRCm39) |
|
probably null |
Het |
Styx |
A |
G |
14: 45,605,909 (GRCm39) |
T138A |
probably benign |
Het |
Sv2c |
A |
T |
13: 96,112,571 (GRCm39) |
L642* |
probably null |
Het |
Taf7 |
T |
C |
18: 37,776,498 (GRCm39) |
E23G |
probably damaging |
Het |
Tcp10a |
A |
T |
17: 7,612,425 (GRCm39) |
T406S |
possibly damaging |
Het |
Tnrc6b |
T |
A |
15: 80,765,017 (GRCm39) |
S840T |
probably benign |
Het |
Tns3 |
A |
G |
11: 8,442,245 (GRCm39) |
I706T |
probably damaging |
Het |
Tpsab1 |
A |
G |
17: 25,564,346 (GRCm39) |
V36A |
probably benign |
Het |
Trafd1 |
T |
A |
5: 121,511,342 (GRCm39) |
D492V |
probably damaging |
Het |
Trp53 |
A |
G |
11: 69,478,244 (GRCm39) |
E51G |
probably benign |
Het |
Vdr |
C |
T |
15: 97,755,477 (GRCm39) |
A349T |
probably benign |
Het |
Vmn2r59 |
T |
C |
7: 41,695,491 (GRCm39) |
D307G |
probably benign |
Het |
Zfp365 |
C |
A |
10: 67,733,437 (GRCm39) |
V252F |
probably damaging |
Het |
Zfp830 |
T |
A |
11: 82,655,803 (GRCm39) |
N202K |
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 |
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 |
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 |
|