Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Accs |
T |
G |
2: 93,845,776 |
K85Q |
probably damaging |
Het |
Acmsd |
A |
T |
1: 127,749,085 |
T116S |
possibly damaging |
Het |
Agrn |
T |
A |
4: 156,172,807 |
K1189* |
probably null |
Het |
Alk |
T |
C |
17: 71,985,460 |
R508G |
probably benign |
Het |
Arhgap23 |
T |
A |
11: 97,491,179 |
Y1123N |
probably damaging |
Het |
Arl6ip5 |
G |
T |
6: 97,232,404 |
M133I |
probably benign |
Het |
Axin2 |
G |
A |
11: 108,942,946 |
G573D |
possibly damaging |
Het |
B4galt2 |
A |
G |
4: 117,876,878 |
|
probably null |
Het |
Baz2b |
G |
T |
2: 59,977,374 |
D180E |
possibly damaging |
Het |
Btnl6 |
G |
T |
17: 34,508,175 |
Y460* |
probably null |
Het |
C530008M17Rik |
T |
C |
5: 76,858,459 |
V889A |
unknown |
Het |
Cct7 |
A |
T |
6: 85,459,149 |
D14V |
probably damaging |
Het |
Cd55 |
T |
A |
1: 130,449,412 |
|
probably benign |
Het |
Cdc45 |
C |
T |
16: 18,798,729 |
M200I |
probably benign |
Het |
Cdh2 |
C |
T |
18: 16,629,480 |
R526Q |
probably benign |
Het |
Chil1 |
A |
C |
1: 134,189,243 |
E315A |
probably damaging |
Het |
Cpm |
C |
A |
10: 117,629,851 |
T43K |
probably damaging |
Het |
Cyp8b1 |
A |
T |
9: 121,915,387 |
V293D |
probably benign |
Het |
Dock1 |
T |
G |
7: 135,163,353 |
D1691E |
probably benign |
Het |
Fasn |
T |
C |
11: 120,809,833 |
D2120G |
probably benign |
Het |
Gal3st4 |
T |
C |
5: 138,265,417 |
K440R |
probably benign |
Het |
Gfpt1 |
A |
T |
6: 87,056,182 |
K130* |
probably null |
Het |
Gpr26 |
T |
C |
7: 131,974,392 |
|
probably null |
Het |
Htr2a |
A |
T |
14: 74,645,062 |
I163F |
probably damaging |
Het |
Insrr |
A |
G |
3: 87,809,572 |
D673G |
probably benign |
Het |
Ipo8 |
G |
T |
6: 148,791,481 |
C636* |
probably null |
Het |
Kirrel |
C |
A |
3: 87,090,473 |
E248* |
probably null |
Het |
Lrp6 |
A |
G |
6: 134,484,265 |
V743A |
probably damaging |
Het |
Lrrc45 |
C |
A |
11: 120,718,318 |
S374R |
probably benign |
Het |
Map3k9 |
G |
A |
12: 81,724,742 |
P714S |
probably benign |
Het |
Mrgprb8 |
T |
A |
7: 48,389,373 |
L264Q |
possibly damaging |
Het |
Mroh4 |
C |
A |
15: 74,606,151 |
W902L |
probably benign |
Het |
Nfat5 |
T |
A |
8: 107,358,735 |
D535E |
probably damaging |
Het |
Nfatc3 |
T |
C |
8: 106,108,185 |
V713A |
probably benign |
Het |
Npc1l1 |
C |
T |
11: 6,214,684 |
V1122M |
possibly damaging |
Het |
Nsg2 |
A |
G |
11: 32,055,011 |
|
probably null |
Het |
Olfr1211 |
C |
A |
2: 88,929,448 |
R289L |
probably damaging |
Het |
Olfr282 |
T |
A |
15: 98,437,779 |
F103L |
probably benign |
Het |
Pax9 |
A |
T |
12: 56,709,819 |
H314L |
possibly damaging |
Het |
Phf21a |
A |
T |
2: 92,360,247 |
I584F |
probably damaging |
Het |
Pip5k1c |
A |
G |
10: 81,313,462 |
E536G |
probably benign |
Het |
Plekhm3 |
A |
G |
1: 64,795,117 |
S736P |
probably damaging |
Het |
Ppil2 |
A |
G |
16: 17,103,602 |
Y73H |
probably benign |
Het |
Ppp3cb |
T |
A |
14: 20,523,577 |
|
probably null |
Het |
Prdm9 |
A |
T |
17: 15,563,260 |
S14R |
probably benign |
Het |
Proc |
A |
G |
18: 32,134,872 |
I71T |
probably damaging |
Het |
Prom2 |
T |
A |
2: 127,538,657 |
|
probably benign |
Het |
Psd |
T |
C |
19: 46,319,545 |
T675A |
probably benign |
Het |
Rnf215 |
G |
T |
11: 4,140,305 |
R341L |
probably damaging |
Het |
Ryr3 |
A |
G |
2: 112,902,576 |
|
probably null |
Het |
Sh2d7 |
C |
A |
9: 54,540,821 |
T42N |
probably benign |
Het |
Sh3glb2 |
C |
T |
2: 30,346,356 |
G279D |
probably benign |
Het |
Slc25a46 |
A |
G |
18: 31,605,815 |
|
probably benign |
Het |
Snx17 |
T |
C |
5: 31,197,046 |
S167P |
probably damaging |
Het |
Snx19 |
A |
G |
9: 30,432,260 |
N572S |
possibly damaging |
Het |
Sptbn4 |
G |
A |
7: 27,367,679 |
R1937C |
probably damaging |
Het |
Srrm1 |
G |
A |
4: 135,325,104 |
P658L |
unknown |
Het |
Srsf11 |
T |
C |
3: 158,016,431 |
|
probably benign |
Het |
Taar7b |
A |
T |
10: 24,000,683 |
M249L |
probably benign |
Het |
Tle6 |
G |
A |
10: 81,600,064 |
Q6* |
probably null |
Het |
Ttc30a2 |
T |
C |
2: 75,976,338 |
E610G |
probably benign |
Het |
Twnk |
G |
T |
19: 45,008,118 |
R330L |
probably damaging |
Het |
Unc13a |
C |
A |
8: 71,656,305 |
|
probably benign |
Het |
Vmn2r107 |
A |
G |
17: 20,356,744 |
T335A |
possibly damaging |
Het |
Wdtc1 |
A |
T |
4: 133,297,478 |
S469R |
possibly damaging |
Het |
Zfp382 |
A |
T |
7: 30,133,737 |
Y271F |
probably benign |
Het |
|