Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700003E16Rik |
A |
C |
6: 83,162,371 |
N426T |
probably benign |
Het |
6430548M08Rik |
A |
G |
8: 120,145,588 |
D85G |
probably benign |
Het |
Abcb11 |
C |
T |
2: 69,299,867 |
D282N |
probably damaging |
Het |
Abcg3 |
A |
T |
5: 104,968,234 |
F245I |
probably benign |
Het |
Abhd17a |
G |
T |
10: 80,584,157 |
F231L |
possibly damaging |
Het |
Adgra1 |
A |
T |
7: 139,876,142 |
D562V |
probably damaging |
Het |
Akap7 |
C |
A |
10: 25,289,669 |
|
probably benign |
Het |
Akap9 |
A |
G |
5: 4,046,364 |
D2413G |
probably damaging |
Het |
Akr1c18 |
A |
T |
13: 4,137,237 |
C193S |
probably damaging |
Het |
Aloxe3 |
A |
T |
11: 69,132,743 |
M231L |
probably benign |
Het |
Apoh |
A |
G |
11: 108,395,848 |
T33A |
probably benign |
Het |
Atp13a5 |
T |
C |
16: 29,321,749 |
N330D |
probably benign |
Het |
C1ql3 |
T |
G |
2: 13,010,778 |
M24L |
probably benign |
Het |
Cacna1d |
T |
C |
14: 30,123,057 |
N712S |
probably benign |
Het |
Cbs |
T |
C |
17: 31,619,139 |
M379V |
possibly damaging |
Het |
Ccdc167 |
T |
C |
17: 29,705,543 |
D28G |
probably damaging |
Het |
Ccp110 |
A |
T |
7: 118,724,575 |
Q679L |
probably benign |
Het |
Ccz1 |
A |
T |
5: 143,998,182 |
L310H |
probably damaging |
Het |
Cerkl |
A |
T |
2: 79,428,760 |
D44E |
probably damaging |
Het |
Cfap221 |
T |
A |
1: 119,995,098 |
E38V |
possibly damaging |
Het |
Chia1 |
T |
A |
3: 106,132,015 |
*474R |
probably null |
Het |
Clint1 |
C |
T |
11: 45,883,763 |
T32M |
probably damaging |
Het |
Clk3 |
A |
T |
9: 57,760,956 |
F227L |
probably damaging |
Het |
Col5a3 |
C |
T |
9: 20,793,946 |
|
probably null |
Het |
Cul2 |
T |
C |
18: 3,426,873 |
I501T |
probably benign |
Het |
Dag1 |
G |
A |
9: 108,209,093 |
A283V |
possibly damaging |
Het |
Ddr2 |
A |
T |
1: 169,982,078 |
W777R |
probably damaging |
Het |
Deaf1 |
A |
T |
7: 141,322,958 |
V151D |
probably damaging |
Het |
Dido1 |
A |
T |
2: 180,675,121 |
V631E |
possibly damaging |
Het |
Dpp4 |
G |
A |
2: 62,358,901 |
Q429* |
probably null |
Het |
Dscaml1 |
A |
G |
9: 45,752,916 |
R2030G |
probably benign |
Het |
Dsel |
C |
T |
1: 111,861,573 |
G411S |
probably damaging |
Het |
E2f8 |
T |
A |
7: 48,867,965 |
M697L |
probably damaging |
Het |
Eef2kmt |
C |
A |
16: 5,247,435 |
G303W |
probably damaging |
Het |
Eif2ak1 |
A |
G |
5: 143,877,671 |
Y182C |
probably damaging |
Het |
Epha6 |
G |
T |
16: 59,960,430 |
A636E |
probably damaging |
Het |
Fancd2 |
G |
A |
6: 113,536,939 |
V95I |
probably benign |
Het |
Fbln5 |
A |
T |
12: 101,760,816 |
C292S |
probably damaging |
Het |
Fgfr4 |
A |
G |
13: 55,159,155 |
Y219C |
probably damaging |
Het |
Frem1 |
T |
G |
4: 82,994,122 |
K670T |
probably damaging |
Het |
Gas2l2 |
A |
T |
11: 83,421,990 |
L832* |
probably null |
Het |
Gbe1 |
A |
G |
16: 70,361,015 |
T101A |
probably benign |
Het |
Gm5114 |
T |
A |
7: 39,408,756 |
I480F |
probably damaging |
Het |
Gm7145 |
A |
T |
1: 117,986,112 |
R241S |
probably damaging |
Het |
Gnal |
G |
A |
18: 67,135,525 |
V161I |
probably benign |
Het |
Gtpbp1 |
T |
C |
15: 79,691,042 |
C46R |
probably benign |
Het |
Gucy2c |
A |
T |
6: 136,702,748 |
L971Q |
probably damaging |
Het |
Hsp90b1 |
T |
C |
10: 86,692,183 |
E740G |
probably damaging |
Het |
Lingo2 |
G |
A |
4: 35,709,450 |
L177F |
possibly damaging |
Het |
Mfsd6l |
A |
G |
11: 68,557,048 |
T242A |
possibly damaging |
Het |
Mmadhc |
C |
T |
2: 50,291,445 |
R71K |
probably damaging |
Het |
Mrm3 |
G |
T |
11: 76,249,900 |
V245L |
probably damaging |
Het |
Nav3 |
T |
A |
10: 109,903,758 |
I117F |
probably damaging |
Het |
Noc3l |
A |
T |
19: 38,795,024 |
V636D |
probably damaging |
Het |
Nwd1 |
A |
T |
8: 72,711,782 |
Q1486L |
probably damaging |
Het |
Olfr1205 |
T |
G |
2: 88,831,846 |
I243R |
probably damaging |
Het |
Olfr1380 |
A |
G |
11: 49,564,502 |
T194A |
possibly damaging |
Het |
Olfr139 |
G |
T |
11: 74,044,900 |
R125S |
possibly damaging |
Het |
Olfr433 |
A |
T |
1: 174,042,853 |
K301M |
probably damaging |
Het |
Olfr785 |
C |
G |
10: 129,409,983 |
L206V |
possibly damaging |
Het |
Pax9 |
T |
A |
12: 56,695,862 |
M1K |
probably null |
Het |
Pcdha1 |
T |
C |
18: 36,930,649 |
V122A |
probably damaging |
Het |
Pgpep1l |
A |
T |
7: 68,237,721 |
S44T |
probably damaging |
Het |
Pla2g3 |
C |
T |
11: 3,493,022 |
L452F |
possibly damaging |
Het |
Plbd2 |
G |
A |
5: 120,493,149 |
R188W |
probably damaging |
Het |
Ppp1r42 |
G |
A |
1: 9,968,857 |
P346L |
probably benign |
Het |
Prdm8 |
T |
A |
5: 98,184,516 |
V92D |
probably damaging |
Het |
Ripor2 |
C |
A |
13: 24,701,444 |
S554* |
probably null |
Het |
Rps19 |
T |
C |
7: 24,885,146 |
V4A |
probably damaging |
Het |
Rrm2b |
T |
A |
15: 37,944,573 |
I159F |
probably benign |
Het |
Rusc1 |
C |
A |
3: 89,091,750 |
G242W |
probably damaging |
Het |
Sarm1 |
A |
G |
11: 78,497,257 |
S68P |
possibly damaging |
Het |
Sctr |
G |
A |
1: 120,022,225 |
R48Q |
probably benign |
Het |
Slc22a4 |
A |
G |
11: 53,986,538 |
F509S |
possibly damaging |
Het |
Slc39a12 |
G |
A |
2: 14,452,000 |
A600T |
probably damaging |
Het |
Spta1 |
A |
T |
1: 174,223,349 |
H1798L |
probably damaging |
Het |
Sulf2 |
T |
G |
2: 166,077,616 |
D804A |
possibly damaging |
Het |
Suz12 |
A |
T |
11: 80,019,703 |
E316D |
probably benign |
Het |
Tbrg4 |
A |
G |
11: 6,620,065 |
S270P |
probably benign |
Het |
Tecta |
T |
C |
9: 42,337,332 |
T1925A |
probably damaging |
Het |
Thrap3 |
A |
T |
4: 126,178,430 |
F390I |
probably damaging |
Het |
Tpr |
C |
A |
1: 150,393,494 |
A70E |
unknown |
Het |
Trpv4 |
G |
C |
5: 114,636,459 |
P188R |
probably benign |
Het |
Txlna |
A |
C |
4: 129,632,160 |
L298R |
probably damaging |
Het |
Ubr4 |
T |
C |
4: 139,413,438 |
S1223P |
probably benign |
Het |
Ucp1 |
A |
T |
8: 83,295,252 |
T238S |
probably damaging |
Het |
Ush2a |
A |
G |
1: 188,415,746 |
S957G |
probably benign |
Het |
Usp34 |
A |
G |
11: 23,488,868 |
N3496D |
|
Het |
Vmn2r50 |
T |
C |
7: 10,050,350 |
|
probably null |
Het |
Wdr54 |
A |
G |
6: 83,154,939 |
V130A |
probably benign |
Het |
Zfp692 |
A |
T |
11: 58,311,505 |
E362V |
probably damaging |
Het |
Zfp811 |
A |
G |
17: 32,797,513 |
Y518H |
probably damaging |
Het |
Zfp994 |
A |
C |
17: 22,200,068 |
C633W |
probably benign |
Het |
|