Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933405L10Rik |
C |
T |
8: 106,435,606 (GRCm39) |
T88M |
probably damaging |
Het |
9430038I01Rik |
A |
G |
7: 136,978,795 (GRCm39) |
|
probably benign |
Het |
Adgra3 |
A |
C |
5: 50,118,834 (GRCm39) |
S905A |
probably damaging |
Het |
Adgrv1 |
A |
G |
13: 81,692,652 (GRCm39) |
Y1618H |
probably damaging |
Het |
Anapc15-ps |
T |
C |
10: 95,509,176 (GRCm39) |
T26A |
probably benign |
Het |
Ankrd13d |
T |
C |
19: 4,321,623 (GRCm39) |
K360E |
probably damaging |
Het |
Anks1b |
T |
A |
10: 90,348,751 (GRCm39) |
|
probably null |
Het |
Apob |
T |
C |
12: 8,057,602 (GRCm39) |
F2028S |
possibly damaging |
Het |
Arap3 |
G |
A |
18: 38,108,636 (GRCm39) |
R1265W |
probably damaging |
Het |
Arhgef37 |
A |
G |
18: 61,651,121 (GRCm39) |
Y135H |
probably damaging |
Het |
Armh3 |
A |
C |
19: 45,963,691 (GRCm39) |
S42R |
probably benign |
Het |
Atp1a1 |
T |
C |
3: 101,489,333 (GRCm39) |
T760A |
probably benign |
Het |
Cdc42bpb |
T |
A |
12: 111,289,255 (GRCm39) |
M497L |
probably benign |
Het |
Ces5a |
C |
T |
8: 94,240,859 (GRCm39) |
V413M |
probably damaging |
Het |
Chd5 |
A |
T |
4: 152,470,263 (GRCm39) |
Y1903F |
probably damaging |
Het |
Chd9 |
T |
A |
8: 91,737,422 (GRCm39) |
N1500K |
probably benign |
Het |
Chmp7 |
G |
T |
14: 69,957,248 (GRCm39) |
D303E |
probably benign |
Het |
Chrnb4 |
A |
T |
9: 54,942,102 (GRCm39) |
Y391N |
possibly damaging |
Het |
Crtc1 |
T |
C |
8: 70,840,802 (GRCm39) |
T475A |
probably benign |
Het |
Cyp2c69 |
A |
G |
19: 39,865,972 (GRCm39) |
I207T |
probably benign |
Het |
Dcp1a |
A |
G |
14: 30,240,940 (GRCm39) |
E250G |
probably damaging |
Het |
Ddx20 |
T |
C |
3: 105,586,398 (GRCm39) |
Q649R |
probably benign |
Het |
Defb12 |
T |
A |
8: 19,162,754 (GRCm39) |
K59N |
probably damaging |
Het |
Dpy19l3 |
A |
T |
7: 35,429,185 (GRCm39) |
I85N |
probably damaging |
Het |
Duox2 |
C |
T |
2: 122,122,739 (GRCm39) |
|
probably null |
Het |
Ebi3 |
T |
A |
17: 56,263,679 (GRCm39) |
Y197N |
probably damaging |
Het |
Emc1 |
G |
A |
4: 139,102,823 (GRCm39) |
R994Q |
probably benign |
Het |
Ercc6 |
G |
T |
14: 32,268,777 (GRCm39) |
M530I |
probably damaging |
Het |
Evl |
T |
A |
12: 108,619,255 (GRCm39) |
D70E |
probably damaging |
Het |
Fbln2 |
A |
G |
6: 91,242,757 (GRCm39) |
N819S |
probably damaging |
Het |
Foxk2 |
A |
G |
11: 121,176,363 (GRCm39) |
I170V |
probably benign |
Het |
Gfm1 |
T |
C |
3: 67,342,943 (GRCm39) |
V159A |
probably damaging |
Het |
Gm10837 |
A |
G |
14: 122,728,177 (GRCm39) |
T18A |
unknown |
Het |
Gm12887 |
A |
T |
4: 121,479,227 (GRCm39) |
V25E |
probably damaging |
Het |
Hectd4 |
A |
G |
5: 121,435,243 (GRCm39) |
H985R |
possibly damaging |
Het |
Hsfy2 |
A |
G |
1: 56,675,791 (GRCm39) |
Y249H |
possibly damaging |
Het |
Hspg2 |
T |
C |
4: 137,272,878 (GRCm39) |
V2639A |
probably damaging |
Het |
Igf2r |
A |
G |
17: 12,923,157 (GRCm39) |
|
probably null |
Het |
Invs |
T |
A |
4: 48,422,035 (GRCm39) |
I889N |
probably damaging |
Het |
Kcnq1 |
A |
T |
7: 142,736,857 (GRCm39) |
M209L |
probably benign |
Het |
Klra7 |
A |
G |
6: 130,206,957 (GRCm39) |
I48T |
possibly damaging |
Het |
Krt26 |
CTAGTA |
CTA |
11: 99,224,352 (GRCm39) |
|
probably benign |
Het |
Lrif1 |
T |
A |
3: 106,640,127 (GRCm39) |
V404D |
probably damaging |
Het |
Lrriq1 |
T |
A |
10: 103,063,034 (GRCm39) |
|
probably null |
Het |
Lypd6 |
T |
A |
2: 50,078,774 (GRCm39) |
I90N |
possibly damaging |
Het |
Mbp |
A |
G |
18: 82,602,247 (GRCm39) |
D174G |
probably damaging |
Het |
Megf9 |
G |
T |
4: 70,453,022 (GRCm39) |
P13Q |
probably damaging |
Het |
Myo15b |
A |
T |
11: 115,760,412 (GRCm39) |
T1155S |
probably benign |
Het |
Nherf2 |
C |
T |
17: 24,860,693 (GRCm39) |
S150N |
possibly damaging |
Het |
Nlrp6 |
T |
A |
7: 140,503,006 (GRCm39) |
C371S |
probably damaging |
Het |
Nosip |
T |
A |
7: 44,726,733 (GRCm39) |
|
probably null |
Het |
Nox3 |
G |
T |
17: 3,720,153 (GRCm39) |
P344H |
probably damaging |
Het |
Nup210l |
T |
C |
3: 90,079,393 (GRCm39) |
V959A |
probably damaging |
Het |
Or10d1 |
A |
G |
9: 39,484,031 (GRCm39) |
Y175H |
possibly damaging |
Het |
Or2b2b |
C |
A |
13: 21,858,842 (GRCm39) |
V91L |
probably benign |
Het |
Or2k2 |
T |
C |
4: 58,785,384 (GRCm39) |
I113V |
probably benign |
Het |
Or5b119 |
A |
G |
19: 13,457,295 (GRCm39) |
I89T |
probably benign |
Het |
Or5k8 |
T |
A |
16: 58,644,440 (GRCm39) |
I211F |
probably damaging |
Het |
Osbpl3 |
A |
C |
6: 50,347,123 (GRCm39) |
S25A |
probably damaging |
Het |
Otog |
G |
A |
7: 45,895,707 (GRCm39) |
C107Y |
probably damaging |
Het |
Pax7 |
G |
A |
4: 139,511,802 (GRCm39) |
R260C |
probably damaging |
Het |
Pbrm1 |
A |
T |
14: 30,760,914 (GRCm39) |
I224F |
probably damaging |
Het |
Pcdh1 |
T |
A |
18: 38,325,278 (GRCm39) |
|
probably null |
Het |
Pcnx1 |
T |
C |
12: 82,027,709 (GRCm39) |
L1585P |
probably damaging |
Het |
Pde4c |
C |
T |
8: 71,200,599 (GRCm39) |
H362Y |
probably damaging |
Het |
Pdlim2 |
C |
T |
14: 70,402,228 (GRCm39) |
R296H |
probably damaging |
Het |
Pgm1 |
A |
T |
4: 99,818,675 (GRCm39) |
Q90L |
probably damaging |
Het |
Phlpp1 |
A |
G |
1: 106,271,235 (GRCm39) |
H814R |
probably benign |
Het |
Pknox2 |
A |
T |
9: 36,866,127 (GRCm39) |
M5K |
possibly damaging |
Het |
Pole |
G |
A |
5: 110,478,701 (GRCm39) |
|
probably null |
Het |
Polr1b |
A |
G |
2: 128,944,886 (GRCm39) |
I61V |
probably benign |
Het |
Prelp |
T |
C |
1: 133,842,495 (GRCm39) |
K217E |
probably damaging |
Het |
Prkce |
C |
T |
17: 86,782,974 (GRCm39) |
Q202* |
probably null |
Het |
Psmd2 |
T |
G |
16: 20,475,332 (GRCm39) |
M370R |
probably benign |
Het |
Rimklb |
A |
T |
6: 122,440,968 (GRCm39) |
H68Q |
probably damaging |
Het |
Rnasel |
A |
G |
1: 153,630,420 (GRCm39) |
D312G |
possibly damaging |
Het |
Rxrg |
A |
T |
1: 167,426,321 (GRCm39) |
M1L |
probably benign |
Het |
Scrn1 |
A |
G |
6: 54,499,826 (GRCm39) |
F220L |
possibly damaging |
Het |
Scyl3 |
A |
G |
1: 163,778,244 (GRCm39) |
S461G |
probably benign |
Het |
Serpina1c |
T |
A |
12: 103,861,282 (GRCm39) |
T411S |
probably benign |
Het |
Serpinb6d |
C |
T |
13: 33,855,364 (GRCm39) |
P346L |
probably benign |
Het |
Spg21 |
G |
T |
9: 65,372,618 (GRCm39) |
V17F |
probably damaging |
Het |
Spink5 |
A |
T |
18: 44,132,958 (GRCm39) |
M525L |
probably benign |
Het |
Sun2 |
T |
C |
15: 79,621,764 (GRCm39) |
T155A |
probably benign |
Het |
Tchh |
T |
A |
3: 93,354,087 (GRCm39) |
F1176I |
unknown |
Het |
Tex15 |
T |
A |
8: 34,066,682 (GRCm39) |
D2037E |
probably benign |
Het |
Tfdp2 |
T |
C |
9: 96,199,857 (GRCm39) |
C392R |
possibly damaging |
Het |
Tmem30c |
T |
C |
16: 57,097,143 (GRCm39) |
N139S |
probably benign |
Het |
Tns2 |
C |
T |
15: 102,021,568 (GRCm39) |
|
probably null |
Het |
Trim66 |
T |
C |
7: 109,075,046 (GRCm39) |
E405G |
probably damaging |
Het |
Trpc4 |
T |
A |
3: 54,187,415 (GRCm39) |
F456I |
probably benign |
Het |
Tspo2 |
T |
C |
17: 48,755,818 (GRCm39) |
D108G |
possibly damaging |
Het |
Tyk2 |
A |
T |
9: 21,032,850 (GRCm39) |
C304* |
probably null |
Het |
Vgll4 |
A |
T |
6: 114,839,756 (GRCm39) |
S185T |
probably benign |
Het |
Vmn2r94 |
A |
C |
17: 18,464,732 (GRCm39) |
S519R |
probably benign |
Het |
Vmn2r96 |
T |
G |
17: 18,818,183 (GRCm39) |
S587A |
probably benign |
Het |
Vps4b |
C |
A |
1: 106,706,712 (GRCm39) |
A287S |
possibly damaging |
Het |
Yeats2 |
C |
T |
16: 20,048,314 (GRCm39) |
P1332S |
probably benign |
Het |
Zfp462 |
T |
G |
4: 55,010,010 (GRCm39) |
S659A |
possibly damaging |
Het |
Zfp507 |
C |
T |
7: 35,493,150 (GRCm39) |
R631Q |
probably damaging |
Het |
Zfp764l1 |
A |
C |
7: 126,990,660 (GRCm39) |
D442E |
probably benign |
Het |
Zswim5 |
G |
T |
4: 116,734,896 (GRCm39) |
E80D |
unknown |
Het |
|
Other mutations in Shld2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00157:Shld2
|
APN |
14 |
33,990,582 (GRCm39) |
missense |
probably benign |
0.02 |
IGL00962:Shld2
|
APN |
14 |
33,971,208 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01288:Shld2
|
APN |
14 |
33,981,600 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01302:Shld2
|
APN |
14 |
33,981,684 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01312:Shld2
|
APN |
14 |
33,990,150 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL01444:Shld2
|
APN |
14 |
33,959,514 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01633:Shld2
|
APN |
14 |
33,971,136 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02251:Shld2
|
APN |
14 |
33,990,235 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02927:Shld2
|
APN |
14 |
33,989,658 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03183:Shld2
|
APN |
14 |
33,967,143 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03226:Shld2
|
APN |
14 |
33,990,328 (GRCm39) |
missense |
probably benign |
0.08 |
R0111:Shld2
|
UTSW |
14 |
33,989,686 (GRCm39) |
missense |
probably damaging |
0.98 |
R1170:Shld2
|
UTSW |
14 |
33,990,448 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1348:Shld2
|
UTSW |
14 |
33,990,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467:Shld2
|
UTSW |
14 |
33,990,619 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1467:Shld2
|
UTSW |
14 |
33,990,619 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1538:Shld2
|
UTSW |
14 |
33,990,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R1602:Shld2
|
UTSW |
14 |
33,989,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R1650:Shld2
|
UTSW |
14 |
33,981,574 (GRCm39) |
intron |
probably benign |
|
R1777:Shld2
|
UTSW |
14 |
33,990,130 (GRCm39) |
missense |
probably benign |
0.07 |
R2425:Shld2
|
UTSW |
14 |
33,990,646 (GRCm39) |
missense |
probably damaging |
0.96 |
R3837:Shld2
|
UTSW |
14 |
33,971,142 (GRCm39) |
missense |
probably damaging |
0.99 |
R3838:Shld2
|
UTSW |
14 |
33,967,325 (GRCm39) |
missense |
probably benign |
0.01 |
R3904:Shld2
|
UTSW |
14 |
33,981,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R3964:Shld2
|
UTSW |
14 |
33,981,644 (GRCm39) |
missense |
probably damaging |
1.00 |
R4322:Shld2
|
UTSW |
14 |
33,981,632 (GRCm39) |
missense |
probably damaging |
0.99 |
R4708:Shld2
|
UTSW |
14 |
33,989,790 (GRCm39) |
missense |
probably benign |
0.17 |
R4771:Shld2
|
UTSW |
14 |
33,990,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R4838:Shld2
|
UTSW |
14 |
33,990,582 (GRCm39) |
missense |
probably benign |
0.02 |
R5448:Shld2
|
UTSW |
14 |
33,990,327 (GRCm39) |
missense |
probably benign |
0.32 |
R5874:Shld2
|
UTSW |
14 |
33,967,215 (GRCm39) |
missense |
probably benign |
0.08 |
R6332:Shld2
|
UTSW |
14 |
33,990,129 (GRCm39) |
missense |
probably benign |
0.07 |
R6333:Shld2
|
UTSW |
14 |
33,989,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R6476:Shld2
|
UTSW |
14 |
33,989,971 (GRCm39) |
missense |
probably benign |
0.27 |
R6576:Shld2
|
UTSW |
14 |
33,990,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R7172:Shld2
|
UTSW |
14 |
33,959,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R7574:Shld2
|
UTSW |
14 |
33,959,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R7725:Shld2
|
UTSW |
14 |
33,990,661 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7755:Shld2
|
UTSW |
14 |
33,970,847 (GRCm39) |
missense |
probably damaging |
0.99 |
R7840:Shld2
|
UTSW |
14 |
33,959,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R7881:Shld2
|
UTSW |
14 |
33,989,724 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7947:Shld2
|
UTSW |
14 |
33,990,436 (GRCm39) |
missense |
probably benign |
0.27 |
R8192:Shld2
|
UTSW |
14 |
33,967,173 (GRCm39) |
missense |
probably benign |
0.04 |
R8443:Shld2
|
UTSW |
14 |
33,989,942 (GRCm39) |
missense |
probably benign |
0.00 |
R8492:Shld2
|
UTSW |
14 |
33,967,189 (GRCm39) |
missense |
probably damaging |
0.99 |
R9323:Shld2
|
UTSW |
14 |
33,981,596 (GRCm39) |
missense |
probably damaging |
0.98 |
R9524:Shld2
|
UTSW |
14 |
33,971,245 (GRCm39) |
nonsense |
probably null |
|
X0009:Shld2
|
UTSW |
14 |
33,967,143 (GRCm39) |
missense |
probably benign |
0.02 |
Z1177:Shld2
|
UTSW |
14 |
33,990,555 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Shld2
|
UTSW |
14 |
33,963,428 (GRCm39) |
missense |
probably benign |
0.31 |
|