Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700024B05Rik |
A |
G |
14: 41,997,417 |
Y105C |
probably damaging |
Het |
2610301B20Rik |
A |
G |
4: 10,898,014 |
T199A |
probably benign |
Het |
Acr |
T |
C |
15: 89,569,500 |
S81P |
probably benign |
Het |
Akr1c14 |
T |
C |
13: 4,079,178 |
|
probably null |
Het |
Ank2 |
C |
A |
3: 126,944,850 |
E2375* |
probably null |
Het |
Avpi1 |
A |
G |
19: 42,124,977 |
W14R |
probably damaging |
Het |
Brd4 |
A |
G |
17: 32,199,015 |
V55A |
probably benign |
Het |
Casp8ap2 |
A |
G |
4: 32,639,392 |
N149D |
probably damaging |
Het |
Ccl25 |
A |
T |
8: 4,349,641 |
|
probably benign |
Het |
Celf5 |
A |
G |
10: 81,462,714 |
L299P |
probably damaging |
Het |
Cfap57 |
T |
G |
4: 118,613,126 |
T186P |
possibly damaging |
Het |
Chrm4 |
A |
G |
2: 91,928,347 |
M367V |
probably benign |
Het |
Col1a2 |
A |
T |
6: 4,516,904 |
|
probably benign |
Het |
Crybg3 |
G |
A |
16: 59,554,165 |
P2242L |
probably damaging |
Het |
Cspg4 |
T |
C |
9: 56,888,074 |
V1031A |
probably damaging |
Het |
Dbnl |
C |
A |
11: 5,798,102 |
P313T |
probably benign |
Het |
Dnah1 |
A |
G |
14: 31,264,925 |
F3637L |
probably damaging |
Het |
Dusp10 |
T |
C |
1: 184,037,605 |
V256A |
possibly damaging |
Het |
Erlin2 |
T |
C |
8: 27,031,764 |
V164A |
probably benign |
Het |
Fam110a |
T |
C |
2: 151,970,211 |
D213G |
probably damaging |
Het |
Fkbp1a |
T |
C |
2: 151,557,500 |
|
probably null |
Het |
Foxg1 |
G |
A |
12: 49,384,720 |
|
probably benign |
Het |
Gm12185 |
T |
C |
11: 48,915,999 |
S122G |
probably benign |
Het |
Gm2042 |
A |
T |
12: 87,960,281 |
D456V |
probably damaging |
Het |
Gm8857 |
G |
T |
5: 10,950,551 |
|
probably null |
Het |
Grin2b |
A |
G |
6: 135,923,038 |
Y282H |
probably damaging |
Het |
Gys2 |
T |
C |
6: 142,472,722 |
D27G |
probably benign |
Het |
H2-DMa |
T |
A |
17: 34,136,997 |
|
probably null |
Het |
Hectd4 |
T |
A |
5: 121,364,568 |
I4245N |
possibly damaging |
Het |
Incenp |
A |
G |
19: 9,893,372 |
Y298H |
unknown |
Het |
Ints2 |
C |
T |
11: 86,233,085 |
G626R |
probably damaging |
Het |
Kifc1 |
A |
T |
17: 33,883,697 |
V314E |
probably damaging |
Het |
Lurap1l |
C |
T |
4: 80,911,367 |
P5S |
probably benign |
Het |
Mtmr11 |
A |
G |
3: 96,169,946 |
Y540C |
probably damaging |
Het |
Muc4 |
C |
A |
16: 32,756,324 |
|
probably benign |
Het |
Myh13 |
A |
G |
11: 67,369,316 |
E1860G |
possibly damaging |
Het |
Myl10 |
G |
C |
5: 136,697,971 |
V70L |
probably benign |
Het |
Nbeal1 |
G |
A |
1: 60,310,947 |
G2385D |
probably damaging |
Het |
Ncaph2 |
G |
A |
15: 89,371,356 |
A578T |
probably benign |
Het |
Ncr1 |
T |
C |
7: 4,338,145 |
V8A |
possibly damaging |
Het |
Nutm1 |
T |
C |
2: 112,256,168 |
T73A |
probably damaging |
Het |
Olfm1 |
G |
A |
2: 28,229,336 |
D313N |
probably damaging |
Het |
Olfr1196 |
T |
A |
2: 88,700,820 |
N170Y |
probably damaging |
Het |
Olfr275 |
A |
G |
4: 52,826,089 |
M231V |
probably benign |
Het |
Olfr749 |
A |
G |
14: 50,736,707 |
F152L |
possibly damaging |
Het |
Otog |
T |
A |
7: 46,267,398 |
|
probably null |
Het |
Peak1 |
G |
T |
9: 56,259,707 |
D312E |
probably damaging |
Het |
Plekhg1 |
T |
C |
10: 3,940,251 |
I331T |
probably damaging |
Het |
Polr1b |
T |
C |
2: 129,115,642 |
V539A |
possibly damaging |
Het |
Polr2a |
A |
T |
11: 69,747,213 |
H143Q |
possibly damaging |
Het |
Ppargc1b |
G |
T |
18: 61,307,714 |
A711D |
probably damaging |
Het |
Prnd |
T |
A |
2: 131,953,442 |
C161S |
possibly damaging |
Het |
Prrt4 |
A |
G |
6: 29,171,148 |
L435P |
possibly damaging |
Het |
Psen2 |
C |
T |
1: 180,227,520 |
|
probably null |
Het |
Psg23 |
T |
C |
7: 18,614,744 |
E46G |
possibly damaging |
Het |
Rasgef1b |
C |
T |
5: 99,232,336 |
R350H |
probably damaging |
Het |
Rfxank |
G |
C |
8: 70,138,170 |
P16A |
probably benign |
Het |
Sema6a |
A |
G |
18: 47,248,570 |
I944T |
probably damaging |
Het |
Serpinc1 |
A |
G |
1: 160,997,521 |
T313A |
probably benign |
Het |
Slc27a4 |
T |
C |
2: 29,804,271 |
S36P |
possibly damaging |
Het |
Slc36a1 |
C |
A |
11: 55,223,737 |
R214S |
probably benign |
Het |
Sorl1 |
C |
T |
9: 42,030,983 |
S982N |
possibly damaging |
Het |
Syt1 |
A |
C |
10: 108,690,936 |
D37E |
probably benign |
Het |
Tcl1b5 |
A |
T |
12: 105,176,491 |
D26V |
probably damaging |
Het |
Tenm4 |
A |
T |
7: 96,895,223 |
K2149* |
probably null |
Het |
Ubc |
T |
A |
5: 125,388,174 |
I30F |
probably damaging |
Het |
Ugt1a7c |
A |
T |
1: 88,095,528 |
E136D |
possibly damaging |
Het |
Utp20 |
A |
G |
10: 88,754,475 |
|
probably null |
Het |
Vmn1r159 |
C |
T |
7: 22,842,864 |
V248I |
probably damaging |
Het |
Vmn2r105 |
T |
C |
17: 20,208,612 |
H734R |
probably damaging |
Het |
Wdr60 |
T |
C |
12: 116,211,891 |
M889V |
probably benign |
Het |
Xrcc2 |
T |
G |
5: 25,692,709 |
I81L |
possibly damaging |
Het |
Zfat |
A |
C |
15: 68,181,015 |
I310S |
probably damaging |
Het |
Zfp119a |
A |
G |
17: 55,866,009 |
V278A |
probably benign |
Het |
Zfp53 |
A |
G |
17: 21,500,246 |
K33E |
probably benign |
Het |
Zfp866 |
G |
T |
8: 69,765,841 |
H376Q |
probably damaging |
Het |
|