Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017B05Rik |
A |
T |
9: 57,256,625 |
I822N |
probably damaging |
Het |
9930111J21Rik1 |
A |
G |
11: 48,947,316 |
S815P |
possibly damaging |
Het |
A430033K04Rik |
A |
G |
5: 138,646,450 |
Y199C |
probably benign |
Het |
Afap1l1 |
A |
T |
18: 61,755,661 |
V113E |
probably benign |
Het |
Ahnak2 |
C |
T |
12: 112,773,738 |
C494Y |
possibly damaging |
Het |
Atr |
A |
T |
9: 95,927,213 |
E1981D |
probably benign |
Het |
Bmp7 |
A |
G |
2: 172,872,958 |
Y353H |
probably damaging |
Het |
Capn11 |
C |
T |
17: 45,657,330 |
|
probably benign |
Het |
Ccdc103 |
T |
C |
11: 102,882,693 |
F47S |
probably damaging |
Het |
Cmas |
A |
G |
6: 142,764,421 |
Y130C |
possibly damaging |
Het |
Cntn5 |
T |
C |
9: 10,144,217 |
Y149C |
probably damaging |
Het |
Col12a1 |
A |
C |
9: 79,706,337 |
S75R |
possibly damaging |
Het |
Crat |
G |
A |
2: 30,413,183 |
H31Y |
probably damaging |
Het |
Dnah7a |
A |
G |
1: 53,698,651 |
V41A |
probably benign |
Het |
F5 |
C |
T |
1: 164,186,878 |
R573C |
probably damaging |
Het |
Gcc2 |
A |
G |
10: 58,281,439 |
N1170S |
possibly damaging |
Het |
Gm29666 |
A |
T |
15: 84,914,059 |
C100* |
probably null |
Het |
Gm3573 |
A |
T |
14: 42,187,515 |
Y158N |
possibly damaging |
Het |
Gm5346 |
T |
A |
8: 43,625,183 |
H668L |
probably benign |
Het |
Gm597 |
A |
T |
1: 28,776,893 |
I686N |
probably benign |
Het |
Gtf3c1 |
G |
T |
7: 125,641,621 |
A1968E |
possibly damaging |
Het |
Heg1 |
C |
A |
16: 33,738,268 |
T815K |
probably damaging |
Het |
Herc1 |
TCCC |
TCC |
9: 66,501,188 |
|
probably null |
Het |
Kif17 |
A |
G |
4: 138,274,995 |
Y170C |
probably damaging |
Het |
Kti12 |
G |
A |
4: 108,848,455 |
G189R |
probably benign |
Het |
Lrp4 |
G |
A |
2: 91,511,504 |
A1821T |
probably benign |
Het |
Mamdc4 |
T |
C |
2: 25,566,936 |
I610V |
probably benign |
Het |
Mmp1b |
T |
C |
9: 7,387,914 |
K27E |
probably benign |
Het |
Mob4 |
A |
G |
1: 55,148,429 |
|
probably null |
Het |
Myc |
G |
A |
15: 61,988,279 |
|
probably null |
Het |
Myo5c |
A |
T |
9: 75,289,186 |
I1305F |
probably benign |
Het |
Nprl3 |
A |
G |
11: 32,237,381 |
V292A |
probably damaging |
Het |
Ntng2 |
T |
C |
2: 29,197,090 |
T373A |
probably damaging |
Het |
Olfr1200 |
C |
T |
2: 88,767,884 |
V144I |
probably benign |
Het |
Olfr161 |
T |
A |
16: 3,592,516 |
V40D |
probably damaging |
Het |
Olfr469 |
T |
A |
7: 107,823,188 |
T94S |
probably benign |
Het |
Olfr863-ps1 |
A |
T |
9: 19,941,774 |
L222H |
unknown |
Het |
Pard3 |
T |
C |
8: 127,410,747 |
L859P |
probably damaging |
Het |
Ppcs |
T |
C |
4: 119,419,088 |
D100G |
probably damaging |
Het |
Prkdc |
G |
T |
16: 15,725,461 |
|
probably null |
Het |
Pwwp2b |
T |
C |
7: 139,255,987 |
V448A |
probably benign |
Het |
Rapgef4 |
A |
G |
2: 72,225,775 |
K624R |
probably benign |
Het |
Synj2 |
C |
T |
17: 6,038,015 |
S1447L |
possibly damaging |
Het |
Tfap2a |
T |
A |
13: 40,728,754 |
N25I |
probably damaging |
Het |
Tnxb |
C |
A |
17: 34,709,632 |
Y2673* |
probably null |
Het |
Trim27 |
T |
A |
13: 21,192,454 |
H457Q |
probably damaging |
Het |
Trim72 |
T |
G |
7: 128,010,386 |
F453L |
probably damaging |
Het |
Ubr5 |
A |
T |
15: 38,015,135 |
M877K |
probably damaging |
Het |
Usp10 |
T |
C |
8: 119,951,972 |
L564P |
probably benign |
Het |
Usp54 |
A |
G |
14: 20,577,228 |
V454A |
probably damaging |
Het |
Uspl1 |
T |
A |
5: 149,214,094 |
D701E |
probably benign |
Het |
Zfp35 |
G |
A |
18: 24,002,958 |
V120I |
possibly damaging |
Het |
Zfp712 |
T |
C |
13: 67,041,504 |
T320A |
probably benign |
Het |
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