Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930438A08Rik |
T |
G |
11: 58,184,188 (GRCm39) |
V302G |
|
Het |
A230072I06Rik |
T |
C |
8: 12,329,689 (GRCm39) |
I48T |
unknown |
Het |
Ada |
T |
A |
2: 163,574,275 (GRCm39) |
D127V |
probably damaging |
Het |
Alb |
G |
C |
5: 90,615,214 (GRCm39) |
R242P |
probably damaging |
Het |
Ankrd34c |
T |
C |
9: 89,611,463 (GRCm39) |
R293G |
possibly damaging |
Het |
Ap2b1 |
T |
C |
11: 83,230,256 (GRCm39) |
|
probably null |
Het |
Arhgef16 |
A |
G |
4: 154,375,524 (GRCm39) |
S157P |
probably damaging |
Het |
Atp2b1 |
C |
T |
10: 98,852,830 (GRCm39) |
L1036F |
probably damaging |
Het |
Ccdc27 |
A |
T |
4: 154,112,556 (GRCm39) |
I573N |
probably damaging |
Het |
Cep164 |
T |
C |
9: 45,685,150 (GRCm39) |
E869G |
probably benign |
Het |
Colq |
A |
T |
14: 31,250,292 (GRCm39) |
V381D |
possibly damaging |
Het |
Drc1 |
A |
G |
5: 30,516,958 (GRCm39) |
E519G |
probably benign |
Het |
Drosha |
G |
A |
15: 12,859,522 (GRCm39) |
V577I |
probably benign |
Het |
Epg5 |
C |
T |
18: 78,024,615 (GRCm39) |
Q1157* |
probably null |
Het |
Eqtn |
T |
C |
4: 94,811,944 (GRCm39) |
S150G |
possibly damaging |
Het |
Fam110d |
C |
T |
4: 133,978,959 (GRCm39) |
R173H |
probably damaging |
Het |
Fam216a |
G |
A |
5: 122,505,445 (GRCm39) |
H172Y |
probably damaging |
Het |
Fbxw19 |
T |
A |
9: 109,323,714 (GRCm39) |
D87V |
probably damaging |
Het |
Fgr |
A |
T |
4: 132,722,324 (GRCm39) |
I198F |
probably damaging |
Het |
Flnc |
A |
G |
6: 29,444,049 (GRCm39) |
D621G |
probably benign |
Het |
Flt3 |
A |
C |
5: 147,291,732 (GRCm39) |
Y573D |
probably damaging |
Het |
Git2 |
A |
T |
5: 114,871,296 (GRCm39) |
I603N |
probably damaging |
Het |
Gm4559 |
C |
T |
7: 141,827,553 (GRCm39) |
R183K |
unknown |
Het |
Gnb5 |
T |
C |
9: 75,250,853 (GRCm39) |
F326L |
probably damaging |
Het |
Grm8 |
A |
T |
6: 27,760,257 (GRCm39) |
W358R |
possibly damaging |
Het |
Hoxa3 |
A |
G |
6: 52,149,253 (GRCm39) |
V126A |
unknown |
Het |
Hras |
T |
C |
7: 140,772,064 (GRCm39) |
T144A |
possibly damaging |
Het |
Hyal1 |
G |
A |
9: 107,455,569 (GRCm39) |
R293H |
probably damaging |
Het |
Ifnlr1 |
A |
G |
4: 135,417,919 (GRCm39) |
S49G |
possibly damaging |
Het |
Ighv8-11 |
C |
A |
12: 115,531,005 (GRCm39) |
C41F |
probably benign |
Het |
Jakmip1 |
A |
G |
5: 37,291,617 (GRCm39) |
T689A |
probably damaging |
Het |
Kcnb1 |
T |
C |
2: 167,030,281 (GRCm39) |
H88R |
probably damaging |
Het |
Kcnt2 |
T |
A |
1: 140,498,199 (GRCm39) |
M892K |
probably benign |
Het |
Lrba |
C |
A |
3: 86,648,773 (GRCm39) |
S2507* |
probably null |
Het |
Mbp |
C |
T |
18: 82,572,499 (GRCm39) |
T65I |
probably damaging |
Het |
Muc2 |
A |
T |
7: 141,290,750 (GRCm39) |
Y12F |
|
Het |
Muc4 |
T |
A |
16: 32,576,949 (GRCm39) |
S80T |
|
Het |
Muc5ac |
A |
G |
7: 141,349,991 (GRCm39) |
D579G |
possibly damaging |
Het |
Muc5b |
A |
G |
7: 141,417,760 (GRCm39) |
T3569A |
possibly damaging |
Het |
Myb |
C |
T |
10: 21,032,273 (GRCm39) |
R36H |
probably damaging |
Het |
Myo6 |
T |
C |
9: 80,171,548 (GRCm39) |
|
probably null |
Het |
Ogfod1 |
T |
C |
8: 94,763,981 (GRCm39) |
V22A |
probably benign |
Het |
Orai3 |
A |
G |
7: 127,373,236 (GRCm39) |
I246V |
probably damaging |
Het |
Otog |
A |
G |
7: 45,891,185 (GRCm39) |
M68V |
probably benign |
Het |
Pcdh20 |
T |
A |
14: 88,706,589 (GRCm39) |
D237V |
probably damaging |
Het |
Pcdhb18 |
T |
C |
18: 37,624,046 (GRCm39) |
F459L |
probably benign |
Het |
Pik3c2g |
C |
T |
6: 139,599,070 (GRCm39) |
T62M |
possibly damaging |
Het |
Plaa |
T |
C |
4: 94,470,876 (GRCm39) |
Y420C |
probably damaging |
Het |
Ppp1r9b |
C |
T |
11: 94,892,768 (GRCm39) |
A656V |
probably benign |
Het |
Pramel39-ps |
T |
C |
5: 94,451,236 (GRCm39) |
T297A |
probably benign |
Het |
Prg4 |
T |
A |
1: 150,330,696 (GRCm39) |
E659V |
unknown |
Het |
Prlhr |
C |
A |
19: 60,455,583 (GRCm39) |
A328S |
probably benign |
Het |
Prlr |
A |
T |
15: 10,328,464 (GRCm39) |
D313V |
probably benign |
Het |
Prune2 |
C |
T |
19: 17,097,772 (GRCm39) |
T1092I |
probably damaging |
Het |
Psme4 |
T |
A |
11: 30,787,334 (GRCm39) |
L1043H |
probably damaging |
Het |
Ptprr |
T |
C |
10: 116,087,084 (GRCm39) |
V521A |
probably benign |
Het |
Rab44 |
A |
T |
17: 29,367,179 (GRCm39) |
D703V |
unknown |
Het |
Rpl9-ps1 |
A |
T |
11: 83,535,911 (GRCm39) |
Y179* |
probably null |
Het |
Scg3 |
T |
A |
9: 75,589,332 (GRCm39) |
N107I |
probably benign |
Het |
Slc7a12 |
T |
C |
3: 14,546,509 (GRCm39) |
V218A |
probably benign |
Het |
Sorcs2 |
A |
G |
5: 36,185,322 (GRCm39) |
L918P |
probably damaging |
Het |
Sox1 |
C |
A |
8: 12,446,686 (GRCm39) |
A109E |
probably damaging |
Het |
Syne1 |
T |
A |
10: 5,155,074 (GRCm39) |
M5622L |
probably benign |
Het |
Syne1 |
A |
T |
10: 5,293,416 (GRCm39) |
L1305Q |
probably damaging |
Het |
Tacc2 |
A |
T |
7: 130,224,884 (GRCm39) |
H523L |
probably benign |
Het |
Tas1r2 |
A |
T |
4: 139,396,938 (GRCm39) |
D788V |
probably benign |
Het |
Tcl1b5 |
T |
A |
12: 105,142,694 (GRCm39) |
D7E |
possibly damaging |
Het |
Tesc |
A |
G |
5: 118,194,666 (GRCm39) |
D159G |
possibly damaging |
Het |
Tm2d2 |
G |
T |
8: 25,507,316 (GRCm39) |
|
probably benign |
Het |
Tnfrsf11a |
T |
A |
1: 105,737,171 (GRCm39) |
C93S |
probably damaging |
Het |
Tnfsf4 |
T |
C |
1: 161,244,593 (GRCm39) |
V94A |
probably benign |
Het |
Trav13n-3 |
T |
A |
14: 53,574,964 (GRCm39) |
Y69N |
probably benign |
Het |
Utp20 |
T |
C |
10: 88,590,457 (GRCm39) |
D2339G |
probably benign |
Het |
Vmn1r225 |
A |
G |
17: 20,722,611 (GRCm39) |
I17M |
possibly damaging |
Het |
Vmn2r111 |
T |
C |
17: 22,778,032 (GRCm39) |
N549S |
possibly damaging |
Het |
Vmn2r114 |
G |
T |
17: 23,509,986 (GRCm39) |
Y831* |
probably null |
Het |
Vmn2r72 |
T |
A |
7: 85,401,146 (GRCm39) |
N91I |
probably damaging |
Het |
Zfp846 |
T |
C |
9: 20,499,808 (GRCm39) |
S13P |
possibly damaging |
Het |
Zfp934 |
G |
T |
13: 62,666,327 (GRCm39) |
N116K |
probably benign |
Het |
|