Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc5 |
T |
C |
16: 20,152,479 (GRCm39) |
T1356A |
possibly damaging |
Het |
Ace3 |
A |
G |
11: 105,886,701 (GRCm39) |
T154A |
probably benign |
Het |
Arhgap31 |
C |
A |
16: 38,422,966 (GRCm39) |
Q1033H |
probably damaging |
Het |
C1qtnf1 |
C |
T |
11: 118,337,340 (GRCm39) |
R57* |
probably null |
Het |
Cacna1g |
T |
C |
11: 94,319,962 (GRCm39) |
T1405A |
probably damaging |
Het |
Cacna1i |
A |
G |
15: 80,260,011 (GRCm39) |
|
probably benign |
Het |
Cdca4 |
T |
A |
12: 112,785,734 (GRCm39) |
|
probably null |
Het |
Cpa4 |
T |
A |
6: 30,585,158 (GRCm39) |
M314K |
probably damaging |
Het |
Cpn2 |
A |
T |
16: 30,078,085 (GRCm39) |
S539T |
possibly damaging |
Het |
Crebbp |
A |
G |
16: 3,902,322 (GRCm39) |
S2306P |
probably damaging |
Het |
Cspg4b |
A |
G |
13: 113,488,163 (GRCm39) |
R9G |
|
Het |
Dcaf5 |
T |
C |
12: 80,385,807 (GRCm39) |
H773R |
probably benign |
Het |
Dcun1d2 |
A |
T |
8: 13,311,406 (GRCm39) |
D194E |
probably benign |
Het |
Dnah1 |
G |
T |
14: 30,989,767 (GRCm39) |
R3250S |
possibly damaging |
Het |
Dnajc25 |
A |
C |
4: 59,020,195 (GRCm39) |
K206T |
possibly damaging |
Het |
Dnajc27 |
T |
C |
12: 4,146,325 (GRCm39) |
L118P |
possibly damaging |
Het |
Faap100 |
A |
G |
11: 120,263,003 (GRCm39) |
I785T |
probably damaging |
Het |
Fam227b |
A |
T |
2: 125,830,928 (GRCm39) |
D425E |
probably benign |
Het |
Fat4 |
C |
G |
3: 39,064,842 (GRCm39) |
L4933V |
probably damaging |
Het |
Fbrsl1 |
A |
G |
5: 110,526,086 (GRCm39) |
F39L |
probably damaging |
Het |
Fezf1 |
A |
G |
6: 23,247,769 (GRCm39) |
V102A |
probably benign |
Het |
Gabra2 |
T |
C |
5: 71,170,040 (GRCm39) |
|
probably benign |
Het |
Garnl3 |
C |
A |
2: 32,916,106 (GRCm39) |
R346L |
probably damaging |
Het |
Grin2a |
A |
T |
16: 9,403,089 (GRCm39) |
I799N |
possibly damaging |
Het |
Hspa4 |
A |
G |
11: 53,160,691 (GRCm39) |
F462L |
probably damaging |
Het |
Iars1 |
C |
A |
13: 49,856,675 (GRCm39) |
|
probably benign |
Het |
Igkv6-32 |
C |
T |
6: 70,051,063 (GRCm39) |
V98M |
possibly damaging |
Het |
Il31ra |
A |
G |
13: 112,662,372 (GRCm39) |
F560S |
possibly damaging |
Het |
Itpr3 |
G |
A |
17: 27,337,651 (GRCm39) |
|
probably benign |
Het |
Kif2a |
G |
A |
13: 107,116,049 (GRCm39) |
T299I |
probably damaging |
Het |
Leo1 |
T |
A |
9: 75,373,544 (GRCm39) |
Y656* |
probably null |
Het |
Lpcat2 |
T |
A |
8: 93,635,864 (GRCm39) |
V422D |
probably damaging |
Het |
Lrrcc1 |
T |
A |
3: 14,601,084 (GRCm39) |
S39T |
probably benign |
Het |
Macf1 |
A |
T |
4: 123,405,869 (GRCm39) |
S341T |
probably benign |
Het |
Mc2r |
T |
A |
18: 68,540,879 (GRCm39) |
Y138F |
probably damaging |
Het |
Mepe |
A |
G |
5: 104,485,754 (GRCm39) |
N298S |
possibly damaging |
Het |
Mmp15 |
C |
A |
8: 96,092,982 (GRCm39) |
N120K |
possibly damaging |
Het |
Mrps9 |
A |
G |
1: 42,918,915 (GRCm39) |
R106G |
probably damaging |
Het |
Muc16 |
T |
A |
9: 18,557,744 (GRCm39) |
M2850L |
unknown |
Het |
Mxra8 |
T |
A |
4: 155,927,122 (GRCm39) |
I352N |
probably damaging |
Het |
Myo16 |
G |
A |
8: 10,411,042 (GRCm39) |
V167I |
unknown |
Het |
Neb |
T |
C |
2: 52,215,051 (GRCm39) |
D209G |
probably damaging |
Het |
Nlgn2 |
A |
G |
11: 69,716,309 (GRCm39) |
V744A |
probably benign |
Het |
Notch2 |
A |
G |
3: 98,029,218 (GRCm39) |
|
probably null |
Het |
Nr1d1 |
G |
C |
11: 98,660,073 (GRCm39) |
R484G |
probably damaging |
Het |
Or14c42-ps1 |
A |
T |
7: 86,211,147 (GRCm39) |
H69L |
unknown |
Het |
Or5ak20 |
T |
C |
2: 85,183,953 (GRCm39) |
T106A |
probably benign |
Het |
Or5k16 |
G |
A |
16: 58,736,843 (GRCm39) |
R54C |
probably benign |
Het |
Or9k2b |
T |
C |
10: 130,016,702 (GRCm39) |
I16V |
probably benign |
Het |
Oxa1l |
A |
G |
14: 54,605,248 (GRCm39) |
|
probably null |
Het |
Piwil4 |
T |
C |
9: 14,616,322 (GRCm39) |
D15G |
|
Het |
Plcz1 |
C |
A |
6: 139,949,612 (GRCm39) |
W461L |
probably damaging |
Het |
Plek |
A |
T |
11: 16,944,676 (GRCm39) |
I118N |
probably damaging |
Het |
Poc1b |
C |
A |
10: 99,000,728 (GRCm39) |
|
probably benign |
Het |
Potefam1 |
A |
T |
2: 111,059,567 (GRCm39) |
M64K |
possibly damaging |
Het |
Ppp1r16b |
G |
A |
2: 158,593,098 (GRCm39) |
D226N |
probably damaging |
Het |
Prss36 |
T |
C |
7: 127,532,635 (GRCm39) |
T739A |
possibly damaging |
Het |
Psme2 |
A |
T |
14: 55,827,074 (GRCm39) |
|
probably null |
Het |
Ptprb |
T |
G |
10: 116,203,495 (GRCm39) |
V1802G |
probably damaging |
Het |
Rabep2 |
C |
A |
7: 126,034,848 (GRCm39) |
Y84* |
probably null |
Het |
Rbbp6 |
T |
G |
7: 122,600,516 (GRCm39) |
S1508A |
unknown |
Het |
Rel |
A |
T |
11: 23,692,430 (GRCm39) |
D534E |
probably benign |
Het |
Rpgrip1 |
G |
A |
14: 52,396,852 (GRCm39) |
S1258N |
probably damaging |
Het |
Rprml |
T |
C |
11: 103,540,953 (GRCm39) |
L116P |
probably damaging |
Het |
Rsph10b |
A |
G |
5: 143,887,112 (GRCm39) |
T323A |
possibly damaging |
Het |
Rtn4rl1 |
A |
G |
11: 75,156,099 (GRCm39) |
H177R |
probably damaging |
Het |
Sag |
A |
G |
1: 87,738,032 (GRCm39) |
T24A |
probably benign |
Het |
Scgb2b26 |
G |
T |
7: 33,643,784 (GRCm39) |
T52N |
probably damaging |
Het |
Scn10a |
T |
C |
9: 119,501,194 (GRCm39) |
I197V |
probably damaging |
Het |
Sec24c |
T |
A |
14: 20,742,927 (GRCm39) |
V1003D |
possibly damaging |
Het |
Sirt2 |
G |
A |
7: 28,471,261 (GRCm39) |
G30E |
probably damaging |
Het |
Slc13a5 |
T |
A |
11: 72,149,919 (GRCm39) |
Q197L |
probably benign |
Het |
Slc44a3 |
A |
T |
3: 121,283,918 (GRCm39) |
S445T |
probably damaging |
Het |
Slc7a7 |
A |
T |
14: 54,610,449 (GRCm39) |
V399E |
probably benign |
Het |
Smarcad1 |
T |
A |
6: 65,088,865 (GRCm39) |
D1000E |
probably benign |
Het |
Sorcs2 |
G |
T |
5: 36,196,657 (GRCm39) |
Q663K |
probably benign |
Het |
Stat4 |
A |
G |
1: 52,118,991 (GRCm39) |
R345G |
probably null |
Het |
Sycp2 |
G |
A |
2: 177,992,768 (GRCm39) |
R1261C |
probably damaging |
Het |
Tcf19 |
T |
C |
17: 35,825,381 (GRCm39) |
I259V |
probably benign |
Het |
Thada |
T |
A |
17: 84,536,637 (GRCm39) |
R1636S |
probably benign |
Het |
Tnrc6c |
T |
C |
11: 117,604,961 (GRCm39) |
L32P |
probably benign |
Het |
Tonsl |
G |
A |
15: 76,517,076 (GRCm39) |
T881I |
probably benign |
Het |
Tonsl |
A |
C |
15: 76,518,263 (GRCm39) |
C570G |
probably damaging |
Het |
Ube2o |
C |
A |
11: 116,432,273 (GRCm39) |
E898* |
probably null |
Het |
Usp5 |
T |
C |
6: 124,794,394 (GRCm39) |
H762R |
possibly damaging |
Het |
Vmn2r15 |
A |
G |
5: 109,434,779 (GRCm39) |
S642P |
probably benign |
Het |
Vmn2r23 |
T |
C |
6: 123,690,431 (GRCm39) |
W436R |
probably damaging |
Het |
Vps13d |
A |
C |
4: 144,811,977 (GRCm39) |
I3343M |
|
Het |
Wbp11 |
T |
C |
6: 136,799,932 (GRCm39) |
K83E |
probably damaging |
Het |
Zfp26 |
T |
A |
9: 20,356,201 (GRCm39) |
N36Y |
possibly damaging |
Het |
Zfp57 |
T |
A |
17: 37,320,938 (GRCm39) |
I264N |
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 |
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 |
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 |
|