Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrf3 |
G |
A |
5: 30,404,489 (GRCm39) |
H316Y |
possibly damaging |
Het |
Adgrf5 |
A |
G |
17: 43,739,477 (GRCm39) |
Y72C |
possibly damaging |
Het |
Ak5 |
T |
A |
3: 152,366,274 (GRCm39) |
L42F |
probably damaging |
Het |
Alas1 |
T |
C |
9: 106,118,489 (GRCm39) |
E211G |
probably damaging |
Het |
Alkbh1 |
C |
T |
12: 87,490,520 (GRCm39) |
|
probably benign |
Het |
Als2cl |
T |
C |
9: 110,714,506 (GRCm39) |
V118A |
probably benign |
Het |
Ano1 |
G |
C |
7: 144,165,127 (GRCm39) |
L641V |
probably damaging |
Het |
Arfgef1 |
C |
T |
1: 10,258,977 (GRCm39) |
|
probably null |
Het |
Atf6b |
A |
T |
17: 34,867,549 (GRCm39) |
|
probably null |
Het |
Atf7ip |
T |
G |
6: 136,586,346 (GRCm39) |
|
probably benign |
Het |
Atp2b4 |
G |
T |
1: 133,654,275 (GRCm39) |
Q777K |
probably benign |
Het |
Baz2a |
T |
A |
10: 127,949,447 (GRCm39) |
S347R |
probably damaging |
Het |
C2cd3 |
T |
C |
7: 100,104,700 (GRCm39) |
|
probably benign |
Het |
Cage1 |
A |
G |
13: 38,207,356 (GRCm39) |
V163A |
probably benign |
Het |
Cdh12 |
T |
A |
15: 21,583,826 (GRCm39) |
N555K |
probably benign |
Het |
Cenpj |
G |
A |
14: 56,801,412 (GRCm39) |
P187L |
possibly damaging |
Het |
Cep112 |
T |
A |
11: 108,410,087 (GRCm39) |
|
probably null |
Het |
Cfap54 |
A |
T |
10: 92,778,841 (GRCm39) |
|
probably benign |
Het |
Cgref1 |
T |
G |
5: 31,090,989 (GRCm39) |
D275A |
possibly damaging |
Het |
Clgn |
A |
C |
8: 84,126,607 (GRCm39) |
N103H |
probably benign |
Het |
Corin |
A |
G |
5: 72,473,394 (GRCm39) |
V905A |
possibly damaging |
Het |
Csta1 |
A |
C |
16: 35,942,692 (GRCm39) |
D72E |
probably benign |
Het |
Cul5 |
A |
T |
9: 53,578,456 (GRCm39) |
L44Q |
probably damaging |
Het |
Dmbt1 |
G |
A |
7: 130,707,900 (GRCm39) |
A1381T |
possibly damaging |
Het |
Dync1i2 |
G |
A |
2: 71,080,197 (GRCm39) |
|
probably null |
Het |
Enoph1 |
A |
G |
5: 100,207,078 (GRCm39) |
D55G |
probably damaging |
Het |
Fat4 |
T |
A |
3: 38,945,319 (GRCm39) |
M1404K |
possibly damaging |
Het |
Fhip2b |
A |
G |
14: 70,822,489 (GRCm39) |
V744A |
possibly damaging |
Het |
Foxi2 |
G |
T |
7: 135,012,406 (GRCm39) |
G98V |
probably damaging |
Het |
Galr2 |
T |
C |
11: 116,173,765 (GRCm39) |
S132P |
probably damaging |
Het |
Gcm2 |
T |
C |
13: 41,263,430 (GRCm39) |
M1V |
probably null |
Het |
Gm15446 |
C |
T |
5: 110,090,362 (GRCm39) |
H205Y |
probably damaging |
Het |
Gm21775 |
T |
A |
Y: 10,553,910 (GRCm39) |
I153N |
probably benign |
Het |
Grip1 |
A |
G |
10: 119,874,603 (GRCm39) |
K789R |
possibly damaging |
Het |
Gsk3b |
T |
A |
16: 38,008,271 (GRCm39) |
D192E |
probably benign |
Het |
Herc2 |
T |
A |
7: 55,813,645 (GRCm39) |
H2625Q |
probably damaging |
Het |
Hoxc9 |
A |
G |
15: 102,892,555 (GRCm39) |
D256G |
probably benign |
Het |
Il7 |
A |
T |
3: 7,638,975 (GRCm39) |
N130K |
probably damaging |
Het |
Irf2 |
A |
T |
8: 47,260,380 (GRCm39) |
N104I |
probably damaging |
Het |
Kat6a |
A |
G |
8: 23,429,321 (GRCm39) |
N1559D |
possibly damaging |
Het |
Kcnq4 |
G |
T |
4: 120,555,199 (GRCm39) |
F661L |
probably benign |
Het |
Kdm5b |
T |
A |
1: 134,540,952 (GRCm39) |
D681E |
probably benign |
Het |
Khdrbs1 |
T |
C |
4: 129,619,514 (GRCm39) |
E209G |
probably damaging |
Het |
Lama3 |
A |
T |
18: 12,661,390 (GRCm39) |
R2116S |
probably damaging |
Het |
Mir124-2hg |
C |
A |
3: 17,839,877 (GRCm39) |
E65* |
probably null |
Het |
Mphosph10 |
T |
A |
7: 64,026,499 (GRCm39) |
L650F |
probably damaging |
Het |
Mrpl48 |
T |
C |
7: 100,198,540 (GRCm39) |
E204G |
probably damaging |
Het |
Msl3l2 |
T |
A |
10: 55,992,040 (GRCm39) |
L255Q |
probably damaging |
Het |
Mx1 |
T |
A |
16: 97,255,379 (GRCm39) |
K225* |
probably null |
Het |
Nf1 |
T |
C |
11: 79,447,549 (GRCm39) |
V435A |
probably damaging |
Het |
Nid1 |
A |
C |
13: 13,675,058 (GRCm39) |
H926P |
probably benign |
Het |
Nlrp9a |
T |
A |
7: 26,256,787 (GRCm39) |
I46K |
possibly damaging |
Het |
Nop2 |
T |
A |
6: 125,116,823 (GRCm39) |
M359K |
probably null |
Het |
Nox1 |
T |
C |
X: 132,995,993 (GRCm39) |
|
probably benign |
Het |
Ogdhl |
G |
A |
14: 32,054,841 (GRCm39) |
R263K |
probably damaging |
Het |
Or14c40 |
A |
T |
7: 86,313,591 (GRCm39) |
K240N |
probably damaging |
Het |
Or2y16 |
T |
A |
11: 49,335,278 (GRCm39) |
V200E |
probably damaging |
Het |
Pbsn |
T |
C |
X: 76,891,582 (GRCm39) |
K72E |
probably damaging |
Het |
Pde12 |
T |
C |
14: 26,390,035 (GRCm39) |
I225V |
probably benign |
Het |
Ppt2 |
A |
T |
17: 34,841,818 (GRCm39) |
|
probably benign |
Het |
Prl3a1 |
A |
G |
13: 27,454,127 (GRCm39) |
D35G |
probably benign |
Het |
Prss3b |
G |
A |
6: 41,009,315 (GRCm39) |
T173I |
probably benign |
Het |
Ptprk |
T |
A |
10: 28,442,599 (GRCm39) |
I893N |
probably damaging |
Het |
Ptprz1 |
T |
C |
6: 22,986,322 (GRCm39) |
|
probably benign |
Het |
Rab3c |
A |
G |
13: 110,397,050 (GRCm39) |
V72A |
probably damaging |
Het |
Rbms2 |
A |
G |
10: 127,973,387 (GRCm39) |
S251P |
probably benign |
Het |
Rfwd3 |
A |
G |
8: 112,024,127 (GRCm39) |
V65A |
probably benign |
Het |
Rps6kl1 |
T |
A |
12: 85,186,397 (GRCm39) |
Y211F |
probably benign |
Het |
Saal1 |
T |
C |
7: 46,348,880 (GRCm39) |
Q317R |
probably damaging |
Het |
Scg3 |
T |
C |
9: 75,572,998 (GRCm39) |
D311G |
probably damaging |
Het |
Sdk2 |
C |
A |
11: 113,745,158 (GRCm39) |
M712I |
probably damaging |
Het |
Serinc2 |
T |
G |
4: 130,154,578 (GRCm39) |
Y158S |
probably damaging |
Het |
Serpinb9c |
A |
T |
13: 33,340,854 (GRCm39) |
C81* |
probably null |
Het |
Sgpp2 |
T |
A |
1: 78,393,588 (GRCm39) |
L197Q |
probably damaging |
Het |
Shroom3 |
A |
T |
5: 92,831,643 (GRCm39) |
T40S |
probably damaging |
Het |
Sik1 |
A |
G |
17: 32,067,771 (GRCm39) |
S435P |
probably benign |
Het |
Slc7a3 |
A |
G |
X: 100,124,373 (GRCm39) |
V464A |
probably benign |
Het |
Snd1 |
T |
C |
6: 28,745,206 (GRCm39) |
F517S |
probably damaging |
Het |
Spata13 |
A |
C |
14: 60,997,040 (GRCm39) |
I1165L |
possibly damaging |
Het |
Stat5b |
A |
T |
11: 100,678,158 (GRCm39) |
S652T |
probably benign |
Het |
Stom |
A |
G |
2: 35,206,037 (GRCm39) |
S231P |
probably damaging |
Het |
Sult1b1 |
A |
G |
5: 87,682,892 (GRCm39) |
Y18H |
probably damaging |
Het |
Tgm4 |
T |
C |
9: 122,890,835 (GRCm39) |
I54T |
probably damaging |
Het |
Tmem176b |
G |
A |
6: 48,813,267 (GRCm39) |
T64I |
probably damaging |
Het |
Tmem87a |
A |
T |
2: 120,199,773 (GRCm39) |
I457N |
probably damaging |
Het |
Trim12c |
A |
G |
7: 103,997,398 (GRCm39) |
F53L |
possibly damaging |
Het |
Ttc6 |
T |
A |
12: 57,784,479 (GRCm39) |
D1849E |
probably benign |
Het |
Ubap2l |
A |
T |
3: 89,938,683 (GRCm39) |
|
probably benign |
Het |
Ush2a |
T |
G |
1: 188,113,746 (GRCm39) |
|
probably null |
Het |
Usp17la |
A |
C |
7: 104,510,378 (GRCm39) |
T328P |
probably damaging |
Het |
Ust |
A |
G |
10: 8,083,330 (GRCm39) |
Y349H |
probably damaging |
Het |
V1rd19 |
A |
T |
7: 23,703,259 (GRCm39) |
M242L |
probably benign |
Het |
Vmn1r33 |
T |
A |
6: 66,589,186 (GRCm39) |
M123L |
probably benign |
Het |
Vps13c |
A |
T |
9: 67,768,115 (GRCm39) |
K111N |
probably damaging |
Het |
Vwa3a |
A |
G |
7: 120,358,172 (GRCm39) |
D81G |
probably damaging |
Het |
Zfp318 |
G |
A |
17: 46,707,950 (GRCm39) |
R336Q |
probably damaging |
Het |
Zfp609 |
A |
G |
9: 65,611,716 (GRCm39) |
S416P |
possibly damaging |
Het |
|
Other mutations in St8sia5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01305:St8sia5
|
APN |
18 |
77,342,358 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01320:St8sia5
|
APN |
18 |
77,342,318 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01682:St8sia5
|
APN |
18 |
77,336,196 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01984:St8sia5
|
APN |
18 |
77,336,157 (GRCm39) |
missense |
probably benign |
0.03 |
ANU22:St8sia5
|
UTSW |
18 |
77,342,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R0194:St8sia5
|
UTSW |
18 |
77,342,420 (GRCm39) |
missense |
probably benign |
0.13 |
R0392:St8sia5
|
UTSW |
18 |
77,342,102 (GRCm39) |
missense |
probably damaging |
1.00 |
R0622:St8sia5
|
UTSW |
18 |
77,333,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R0696:St8sia5
|
UTSW |
18 |
77,342,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R1231:St8sia5
|
UTSW |
18 |
77,320,502 (GRCm39) |
missense |
probably damaging |
0.97 |
R1559:St8sia5
|
UTSW |
18 |
77,299,460 (GRCm39) |
critical splice donor site |
probably null |
|
R2058:St8sia5
|
UTSW |
18 |
77,342,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R2268:St8sia5
|
UTSW |
18 |
77,320,526 (GRCm39) |
missense |
probably damaging |
0.99 |
R4399:St8sia5
|
UTSW |
18 |
77,340,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R4926:St8sia5
|
UTSW |
18 |
77,342,478 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5986:St8sia5
|
UTSW |
18 |
77,342,478 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6301:St8sia5
|
UTSW |
18 |
77,333,836 (GRCm39) |
missense |
probably damaging |
0.98 |
R7020:St8sia5
|
UTSW |
18 |
77,333,876 (GRCm39) |
missense |
probably damaging |
0.97 |
R7087:St8sia5
|
UTSW |
18 |
77,342,238 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7784:St8sia5
|
UTSW |
18 |
77,342,246 (GRCm39) |
missense |
probably benign |
0.36 |
R8037:St8sia5
|
UTSW |
18 |
77,336,238 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8153:St8sia5
|
UTSW |
18 |
77,340,807 (GRCm39) |
critical splice donor site |
probably null |
|
R8544:St8sia5
|
UTSW |
18 |
77,342,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R8858:St8sia5
|
UTSW |
18 |
77,320,511 (GRCm39) |
missense |
probably benign |
0.01 |
R8906:St8sia5
|
UTSW |
18 |
77,336,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R8980:St8sia5
|
UTSW |
18 |
77,333,761 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9294:St8sia5
|
UTSW |
18 |
77,342,525 (GRCm39) |
missense |
probably damaging |
1.00 |
|