Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
T |
A |
11: 109,870,781 (GRCm39) |
I124L |
probably benign |
Het |
Abi3bp |
A |
G |
16: 56,394,862 (GRCm39) |
Y190C |
probably damaging |
Het |
Adam34 |
A |
C |
8: 44,104,843 (GRCm39) |
N267K |
probably benign |
Het |
Anxa5 |
T |
C |
3: 36,503,551 (GRCm39) |
D301G |
probably damaging |
Het |
Atf7ip |
G |
T |
6: 136,536,886 (GRCm39) |
D40Y |
probably damaging |
Het |
Cacna2d2 |
T |
G |
9: 107,391,071 (GRCm39) |
M400R |
probably damaging |
Het |
Cd96 |
C |
A |
16: 45,938,335 (GRCm39) |
L43F |
probably damaging |
Het |
Cep120 |
T |
C |
18: 53,871,560 (GRCm39) |
E104G |
probably damaging |
Het |
Cfap221 |
T |
C |
1: 119,881,389 (GRCm39) |
I358V |
probably benign |
Het |
Cfhr4 |
C |
T |
1: 139,702,398 (GRCm39) |
E29K |
probably damaging |
Het |
Chil4 |
C |
T |
3: 106,113,414 (GRCm39) |
E168K |
probably benign |
Het |
Clca3a1 |
A |
G |
3: 144,452,590 (GRCm39) |
V631A |
probably damaging |
Het |
Cluh |
C |
T |
11: 74,552,902 (GRCm39) |
A649V |
possibly damaging |
Het |
Commd9 |
A |
G |
2: 101,727,502 (GRCm39) |
T99A |
probably benign |
Het |
Csgalnact1 |
T |
C |
8: 68,854,036 (GRCm39) |
N255S |
probably benign |
Het |
Cyth3 |
T |
A |
5: 143,683,516 (GRCm39) |
H138Q |
possibly damaging |
Het |
Dnah7a |
A |
T |
1: 53,495,691 (GRCm39) |
|
probably benign |
Het |
Fbxl18 |
G |
A |
5: 142,871,978 (GRCm39) |
A419V |
probably damaging |
Het |
Fyco1 |
A |
G |
9: 123,652,303 (GRCm39) |
V1135A |
probably benign |
Het |
Glcci1 |
C |
A |
6: 8,537,837 (GRCm39) |
H152N |
probably benign |
Het |
Gm10477 |
T |
A |
X: 55,570,127 (GRCm39) |
F9Y |
probably damaging |
Het |
Gnrhr |
A |
G |
5: 86,330,060 (GRCm39) |
L320P |
probably damaging |
Het |
Gorasp1 |
A |
T |
9: 119,759,306 (GRCm39) |
S138T |
probably benign |
Het |
Hars1 |
C |
A |
18: 36,900,294 (GRCm39) |
Q469H |
probably damaging |
Het |
Homer2 |
T |
C |
7: 81,286,111 (GRCm39) |
K34E |
probably damaging |
Het |
Hscb |
T |
C |
5: 110,978,823 (GRCm39) |
I198V |
probably benign |
Het |
Kat6b |
T |
C |
14: 21,567,057 (GRCm39) |
S39P |
probably damaging |
Het |
Kcnk12 |
G |
T |
17: 88,053,499 (GRCm39) |
Q388K |
probably damaging |
Het |
Kcnq3 |
A |
G |
15: 65,874,104 (GRCm39) |
I548T |
probably benign |
Het |
Mark2 |
A |
G |
19: 7,261,880 (GRCm39) |
Y351H |
probably damaging |
Het |
Masp2 |
A |
T |
4: 148,698,952 (GRCm39) |
I678F |
probably damaging |
Het |
Mc4r |
A |
T |
18: 66,992,531 (GRCm39) |
I194N |
probably damaging |
Het |
Ms4a6d |
A |
G |
19: 11,579,223 (GRCm39) |
S85P |
probably damaging |
Het |
Myh4 |
T |
A |
11: 67,145,569 (GRCm39) |
Y1351N |
probably benign |
Het |
Myo16 |
A |
G |
8: 10,322,789 (GRCm39) |
D73G |
probably damaging |
Het |
Mzt1 |
C |
T |
14: 99,278,097 (GRCm39) |
|
probably null |
Het |
Nalcn |
G |
A |
14: 123,521,013 (GRCm39) |
H1631Y |
probably benign |
Het |
Ncf2 |
A |
G |
1: 152,701,661 (GRCm39) |
N213S |
probably benign |
Het |
Nf1 |
C |
A |
11: 79,437,987 (GRCm39) |
T99K |
probably damaging |
Het |
Nsf |
T |
C |
11: 103,749,843 (GRCm39) |
S547G |
probably damaging |
Het |
Ntrk3 |
T |
A |
7: 78,112,587 (GRCm39) |
I190F |
probably benign |
Het |
Obsl1 |
T |
C |
1: 75,474,877 (GRCm39) |
Y841C |
probably damaging |
Het |
Ogdh |
A |
T |
11: 6,290,438 (GRCm39) |
|
probably benign |
Het |
Or2ag12 |
T |
A |
7: 106,277,691 (GRCm39) |
M1L |
probably damaging |
Het |
Or5b12 |
C |
T |
19: 12,896,852 (GRCm39) |
V274M |
probably damaging |
Het |
Otog |
G |
A |
7: 45,918,767 (GRCm39) |
V948I |
probably damaging |
Het |
Plekhm1 |
T |
C |
11: 103,264,824 (GRCm39) |
D880G |
probably benign |
Het |
Pnliprp2 |
G |
T |
19: 58,751,821 (GRCm39) |
V189L |
probably benign |
Het |
Polg |
A |
G |
7: 79,106,241 (GRCm39) |
L678S |
probably benign |
Het |
Ptprm |
C |
T |
17: 66,995,350 (GRCm39) |
V1293I |
probably damaging |
Het |
Pwwp3a |
T |
A |
10: 80,068,442 (GRCm39) |
D195E |
possibly damaging |
Het |
Rhou |
A |
T |
8: 124,387,990 (GRCm39) |
R241W |
probably damaging |
Het |
Rtn4 |
A |
T |
11: 29,686,437 (GRCm39) |
N264I |
probably damaging |
Het |
Sez6l |
T |
C |
5: 112,621,276 (GRCm39) |
|
probably benign |
Het |
Sost |
T |
C |
11: 101,855,069 (GRCm39) |
E80G |
probably damaging |
Het |
Spag16 |
C |
T |
1: 69,935,744 (GRCm39) |
|
probably benign |
Het |
Speer4f2 |
A |
T |
5: 17,579,447 (GRCm39) |
N82I |
probably damaging |
Het |
Spef2 |
C |
T |
15: 9,584,194 (GRCm39) |
E1624K |
probably damaging |
Het |
Taf1b |
T |
A |
12: 24,606,668 (GRCm39) |
L496Q |
possibly damaging |
Het |
Tarbp1 |
A |
G |
8: 127,173,786 (GRCm39) |
I976T |
probably damaging |
Het |
Tex14 |
T |
A |
11: 87,390,431 (GRCm39) |
V376D |
probably damaging |
Het |
Timm21 |
G |
C |
18: 84,967,387 (GRCm39) |
L130V |
probably damaging |
Het |
Tm9sf1 |
T |
C |
14: 55,873,680 (GRCm39) |
D606G |
probably damaging |
Het |
Tmc2 |
A |
C |
2: 130,090,676 (GRCm39) |
N674T |
possibly damaging |
Het |
Top3a |
C |
A |
11: 60,638,810 (GRCm39) |
E562* |
probably null |
Het |
Umodl1 |
A |
T |
17: 31,201,238 (GRCm39) |
D389V |
probably damaging |
Het |
Uso1 |
T |
C |
5: 92,340,718 (GRCm39) |
|
probably benign |
Het |
Vmn1r205 |
A |
G |
13: 22,776,223 (GRCm39) |
V293A |
possibly damaging |
Het |
Vmn2r107 |
A |
G |
17: 20,565,840 (GRCm39) |
T52A |
probably benign |
Het |
Vmn2r4 |
C |
T |
3: 64,298,479 (GRCm39) |
V461I |
possibly damaging |
Het |
Vmn2r99 |
A |
T |
17: 19,582,415 (GRCm39) |
I7F |
probably benign |
Het |
Wdr43 |
A |
G |
17: 71,940,647 (GRCm39) |
S258G |
probably benign |
Het |
Zbtb24 |
A |
G |
10: 41,327,123 (GRCm39) |
D3G |
probably benign |
Het |
Zc3hav1 |
C |
T |
6: 38,309,692 (GRCm39) |
V377I |
possibly damaging |
Het |
Zfp668 |
T |
C |
7: 127,465,654 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Vps11 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01977:Vps11
|
APN |
9 |
44,267,516 (GRCm39) |
splice site |
probably benign |
|
IGL03135:Vps11
|
APN |
9 |
44,267,653 (GRCm39) |
missense |
probably benign |
0.39 |
PIT4696001:Vps11
|
UTSW |
9 |
44,269,486 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0042:Vps11
|
UTSW |
9 |
44,267,588 (GRCm39) |
nonsense |
probably null |
|
R0042:Vps11
|
UTSW |
9 |
44,267,588 (GRCm39) |
nonsense |
probably null |
|
R0122:Vps11
|
UTSW |
9 |
44,265,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R0335:Vps11
|
UTSW |
9 |
44,265,135 (GRCm39) |
missense |
probably null |
0.02 |
R0714:Vps11
|
UTSW |
9 |
44,270,953 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1068:Vps11
|
UTSW |
9 |
44,264,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R1991:Vps11
|
UTSW |
9 |
44,270,524 (GRCm39) |
missense |
probably damaging |
0.97 |
R2068:Vps11
|
UTSW |
9 |
44,269,613 (GRCm39) |
missense |
probably damaging |
0.99 |
R2084:Vps11
|
UTSW |
9 |
44,264,558 (GRCm39) |
missense |
probably benign |
0.14 |
R2103:Vps11
|
UTSW |
9 |
44,270,524 (GRCm39) |
missense |
probably damaging |
0.97 |
R2119:Vps11
|
UTSW |
9 |
44,260,294 (GRCm39) |
missense |
probably benign |
0.01 |
R4160:Vps11
|
UTSW |
9 |
44,267,017 (GRCm39) |
missense |
probably damaging |
0.98 |
R4161:Vps11
|
UTSW |
9 |
44,267,017 (GRCm39) |
missense |
probably damaging |
0.98 |
R4564:Vps11
|
UTSW |
9 |
44,272,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R4879:Vps11
|
UTSW |
9 |
44,264,597 (GRCm39) |
missense |
probably benign |
|
R5629:Vps11
|
UTSW |
9 |
44,267,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R5910:Vps11
|
UTSW |
9 |
44,270,432 (GRCm39) |
splice site |
probably null |
|
R5988:Vps11
|
UTSW |
9 |
44,265,221 (GRCm39) |
missense |
probably benign |
0.01 |
R6430:Vps11
|
UTSW |
9 |
44,272,847 (GRCm39) |
missense |
probably benign |
0.11 |
R7002:Vps11
|
UTSW |
9 |
44,266,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R7147:Vps11
|
UTSW |
9 |
44,266,379 (GRCm39) |
nonsense |
probably null |
|
R7237:Vps11
|
UTSW |
9 |
44,265,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R7261:Vps11
|
UTSW |
9 |
44,265,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R7577:Vps11
|
UTSW |
9 |
44,260,258 (GRCm39) |
missense |
probably benign |
0.01 |
R8093:Vps11
|
UTSW |
9 |
44,267,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R8142:Vps11
|
UTSW |
9 |
44,265,852 (GRCm39) |
missense |
probably benign |
0.05 |
R8238:Vps11
|
UTSW |
9 |
44,264,057 (GRCm39) |
missense |
probably benign |
0.08 |
R8366:Vps11
|
UTSW |
9 |
44,267,052 (GRCm39) |
nonsense |
probably null |
|
R8374:Vps11
|
UTSW |
9 |
44,267,706 (GRCm39) |
missense |
probably benign |
|
R8731:Vps11
|
UTSW |
9 |
44,265,756 (GRCm39) |
missense |
probably benign |
0.00 |
R8742:Vps11
|
UTSW |
9 |
44,267,070 (GRCm39) |
utr 3 prime |
probably benign |
|
R9420:Vps11
|
UTSW |
9 |
44,267,719 (GRCm39) |
missense |
probably benign |
0.14 |
R9474:Vps11
|
UTSW |
9 |
44,260,290 (GRCm39) |
nonsense |
probably null |
|
R9625:Vps11
|
UTSW |
9 |
44,265,738 (GRCm39) |
missense |
probably damaging |
1.00 |
|