Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700003E16Rik |
A |
C |
6: 83,139,353 (GRCm39) |
N426T |
probably benign |
Het |
6430548M08Rik |
A |
G |
8: 120,872,327 (GRCm39) |
D85G |
probably benign |
Het |
Abcb11 |
C |
T |
2: 69,130,211 (GRCm39) |
D282N |
probably damaging |
Het |
Abcg3 |
A |
T |
5: 105,116,100 (GRCm39) |
F245I |
probably benign |
Het |
Abhd17a |
G |
T |
10: 80,419,991 (GRCm39) |
F231L |
possibly damaging |
Het |
Adgra1 |
A |
T |
7: 139,456,058 (GRCm39) |
D562V |
probably damaging |
Het |
Akap7 |
C |
A |
10: 25,165,567 (GRCm39) |
|
probably benign |
Het |
Akap9 |
A |
G |
5: 4,096,364 (GRCm39) |
D2413G |
probably damaging |
Het |
Akr1c18 |
A |
T |
13: 4,187,236 (GRCm39) |
C193S |
probably damaging |
Het |
Aloxe3 |
A |
T |
11: 69,023,569 (GRCm39) |
M231L |
probably benign |
Het |
Apoh |
A |
G |
11: 108,286,674 (GRCm39) |
T33A |
probably benign |
Het |
Atp13a5 |
T |
C |
16: 29,140,567 (GRCm39) |
N330D |
probably benign |
Het |
C1ql3 |
T |
G |
2: 13,015,589 (GRCm39) |
M24L |
probably benign |
Het |
Cacna1d |
T |
C |
14: 29,845,014 (GRCm39) |
N712S |
probably benign |
Het |
Cbs |
T |
C |
17: 31,838,113 (GRCm39) |
M379V |
possibly damaging |
Het |
Ccdc167 |
T |
C |
17: 29,924,517 (GRCm39) |
D28G |
probably damaging |
Het |
Ccp110 |
A |
T |
7: 118,323,798 (GRCm39) |
Q679L |
probably benign |
Het |
Ccz1 |
A |
T |
5: 143,935,000 (GRCm39) |
L310H |
probably damaging |
Het |
Cerkl |
A |
T |
2: 79,259,104 (GRCm39) |
D44E |
probably damaging |
Het |
Cfap221 |
T |
A |
1: 119,922,828 (GRCm39) |
E38V |
possibly damaging |
Het |
Chia1 |
T |
A |
3: 106,039,331 (GRCm39) |
*474R |
probably null |
Het |
Clint1 |
C |
T |
11: 45,774,590 (GRCm39) |
T32M |
probably damaging |
Het |
Clk3 |
A |
T |
9: 57,668,239 (GRCm39) |
F227L |
probably damaging |
Het |
Col5a3 |
C |
T |
9: 20,705,242 (GRCm39) |
|
probably null |
Het |
Cul2 |
T |
C |
18: 3,426,873 (GRCm39) |
I501T |
probably benign |
Het |
Dag1 |
G |
A |
9: 108,086,292 (GRCm39) |
A283V |
possibly damaging |
Het |
Ddr2 |
A |
T |
1: 169,809,647 (GRCm39) |
W777R |
probably damaging |
Het |
Deaf1 |
A |
T |
7: 140,902,871 (GRCm39) |
V151D |
probably damaging |
Het |
Dido1 |
A |
T |
2: 180,316,914 (GRCm39) |
V631E |
possibly damaging |
Het |
Dpp4 |
G |
A |
2: 62,189,245 (GRCm39) |
Q429* |
probably null |
Het |
Dscaml1 |
A |
G |
9: 45,664,214 (GRCm39) |
R2030G |
probably benign |
Het |
Dsel |
C |
T |
1: 111,789,303 (GRCm39) |
G411S |
probably damaging |
Het |
E2f8 |
T |
A |
7: 48,517,713 (GRCm39) |
M697L |
probably damaging |
Het |
Eef2kmt |
C |
A |
16: 5,065,299 (GRCm39) |
G303W |
probably damaging |
Het |
Eif2ak1 |
A |
G |
5: 143,814,489 (GRCm39) |
Y182C |
probably damaging |
Het |
Epha6 |
G |
T |
16: 59,780,793 (GRCm39) |
A636E |
probably damaging |
Het |
Fancd2 |
G |
A |
6: 113,513,900 (GRCm39) |
V95I |
probably benign |
Het |
Fbln5 |
A |
T |
12: 101,727,075 (GRCm39) |
C292S |
probably damaging |
Het |
Fgfr4 |
A |
G |
13: 55,306,968 (GRCm39) |
Y219C |
probably damaging |
Het |
Frem1 |
T |
G |
4: 82,912,359 (GRCm39) |
K670T |
probably damaging |
Het |
Fsip2 |
A |
T |
2: 82,809,711 (GRCm39) |
H2010L |
probably benign |
Het |
Gas2l2 |
A |
T |
11: 83,312,816 (GRCm39) |
L832* |
probably null |
Het |
Gbe1 |
A |
G |
16: 70,157,903 (GRCm39) |
T101A |
probably benign |
Het |
Gm5114 |
T |
A |
7: 39,058,180 (GRCm39) |
I480F |
probably damaging |
Het |
Gm7145 |
A |
T |
1: 117,913,842 (GRCm39) |
R241S |
probably damaging |
Het |
Gnal |
G |
A |
18: 67,268,596 (GRCm39) |
V161I |
probably benign |
Het |
Gtpbp1 |
T |
C |
15: 79,575,243 (GRCm39) |
C46R |
probably benign |
Het |
Gucy2c |
A |
T |
6: 136,679,746 (GRCm39) |
L971Q |
probably damaging |
Het |
Hsp90b1 |
T |
C |
10: 86,528,047 (GRCm39) |
E740G |
probably damaging |
Het |
Lingo2 |
G |
A |
4: 35,709,450 (GRCm39) |
L177F |
possibly damaging |
Het |
Mfsd6l |
A |
G |
11: 68,447,874 (GRCm39) |
T242A |
possibly damaging |
Het |
Mmadhc |
C |
T |
2: 50,181,457 (GRCm39) |
R71K |
probably damaging |
Het |
Mrm3 |
G |
T |
11: 76,140,726 (GRCm39) |
V245L |
probably damaging |
Het |
Nav3 |
T |
A |
10: 109,739,619 (GRCm39) |
I117F |
probably damaging |
Het |
Noc3l |
A |
T |
19: 38,783,468 (GRCm39) |
V636D |
probably damaging |
Het |
Nwd1 |
A |
T |
8: 73,438,410 (GRCm39) |
Q1486L |
probably damaging |
Het |
Or2y10 |
A |
G |
11: 49,455,329 (GRCm39) |
T194A |
possibly damaging |
Het |
Or3a10 |
G |
T |
11: 73,935,726 (GRCm39) |
R125S |
possibly damaging |
Het |
Or4c11c |
T |
G |
2: 88,662,190 (GRCm39) |
I243R |
probably damaging |
Het |
Or6c5b |
C |
G |
10: 129,245,852 (GRCm39) |
L206V |
possibly damaging |
Het |
Pax9 |
T |
A |
12: 56,742,647 (GRCm39) |
M1K |
probably null |
Het |
Pcdha1 |
T |
C |
18: 37,063,702 (GRCm39) |
V122A |
probably damaging |
Het |
Pgpep1l |
A |
T |
7: 67,887,469 (GRCm39) |
S44T |
probably damaging |
Het |
Pla2g3 |
C |
T |
11: 3,443,022 (GRCm39) |
L452F |
possibly damaging |
Het |
Plbd2 |
G |
A |
5: 120,631,214 (GRCm39) |
R188W |
probably damaging |
Het |
Ppp1r42 |
G |
A |
1: 10,039,082 (GRCm39) |
P346L |
probably benign |
Het |
Prdm8 |
T |
A |
5: 98,332,375 (GRCm39) |
V92D |
probably damaging |
Het |
Ripor2 |
C |
A |
13: 24,885,427 (GRCm39) |
S554* |
probably null |
Het |
Rps19 |
T |
C |
7: 24,584,571 (GRCm39) |
V4A |
probably damaging |
Het |
Rrm2b |
T |
A |
15: 37,944,817 (GRCm39) |
I159F |
probably benign |
Het |
Rusc1 |
C |
A |
3: 88,999,057 (GRCm39) |
G242W |
probably damaging |
Het |
Sarm1 |
A |
G |
11: 78,388,083 (GRCm39) |
S68P |
possibly damaging |
Het |
Sctr |
G |
A |
1: 119,949,955 (GRCm39) |
R48Q |
probably benign |
Het |
Slc22a4 |
A |
G |
11: 53,877,364 (GRCm39) |
F509S |
possibly damaging |
Het |
Slc39a12 |
G |
A |
2: 14,456,811 (GRCm39) |
A600T |
probably damaging |
Het |
Spta1 |
A |
T |
1: 174,050,915 (GRCm39) |
H1798L |
probably damaging |
Het |
Sulf2 |
T |
G |
2: 165,919,536 (GRCm39) |
D804A |
possibly damaging |
Het |
Suz12 |
A |
T |
11: 79,910,529 (GRCm39) |
E316D |
probably benign |
Het |
Tbrg4 |
A |
G |
11: 6,570,065 (GRCm39) |
S270P |
probably benign |
Het |
Tecta |
T |
C |
9: 42,248,628 (GRCm39) |
T1925A |
probably damaging |
Het |
Thrap3 |
A |
T |
4: 126,072,223 (GRCm39) |
F390I |
probably damaging |
Het |
Tpr |
C |
A |
1: 150,269,245 (GRCm39) |
A70E |
unknown |
Het |
Trpv4 |
G |
C |
5: 114,774,520 (GRCm39) |
P188R |
probably benign |
Het |
Txlna |
A |
C |
4: 129,525,953 (GRCm39) |
L298R |
probably damaging |
Het |
Ubr4 |
T |
C |
4: 139,140,749 (GRCm39) |
S1223P |
probably benign |
Het |
Ucp1 |
A |
T |
8: 84,021,881 (GRCm39) |
T238S |
probably damaging |
Het |
Ush2a |
A |
G |
1: 188,147,943 (GRCm39) |
S957G |
probably benign |
Het |
Usp34 |
A |
G |
11: 23,438,868 (GRCm39) |
N3496D |
|
Het |
Vmn2r50 |
T |
C |
7: 9,784,277 (GRCm39) |
|
probably null |
Het |
Wdr54 |
A |
G |
6: 83,131,921 (GRCm39) |
V130A |
probably benign |
Het |
Zfp692 |
A |
T |
11: 58,202,331 (GRCm39) |
E362V |
probably damaging |
Het |
Zfp811 |
A |
G |
17: 33,016,487 (GRCm39) |
Y518H |
probably damaging |
Het |
Zfp994 |
A |
C |
17: 22,419,049 (GRCm39) |
C633W |
probably benign |
Het |
|