Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930438A08Rik |
A |
G |
11: 58,178,302 (GRCm39) |
I121V |
probably benign |
Het |
Adprh |
C |
T |
16: 38,266,396 (GRCm39) |
V249I |
probably benign |
Het |
Akap11 |
A |
T |
14: 78,736,402 (GRCm39) |
M1797K |
probably benign |
Het |
Akap6 |
T |
A |
12: 52,933,405 (GRCm39) |
I299N |
probably benign |
Het |
Akr1c12 |
A |
T |
13: 4,322,211 (GRCm39) |
M277K |
possibly damaging |
Het |
Ankrd17 |
A |
T |
5: 90,412,616 (GRCm39) |
M1236K |
probably damaging |
Het |
Arhgef11 |
A |
G |
3: 87,635,313 (GRCm39) |
D874G |
probably damaging |
Het |
Atg4b |
T |
C |
1: 93,715,437 (GRCm39) |
|
probably benign |
Het |
Bcl9 |
G |
A |
3: 97,117,368 (GRCm39) |
P442L |
probably damaging |
Het |
Ccdc107 |
A |
T |
4: 43,495,228 (GRCm39) |
K98* |
probably null |
Het |
Cenpl |
A |
G |
1: 160,913,619 (GRCm39) |
Q343R |
probably benign |
Het |
Cep104 |
T |
C |
4: 154,074,319 (GRCm39) |
C524R |
probably damaging |
Het |
Clec3b |
C |
T |
9: 122,985,827 (GRCm39) |
T75I |
probably benign |
Het |
Col13a1 |
A |
T |
10: 61,741,064 (GRCm39) |
|
probably benign |
Het |
Crot |
C |
T |
5: 9,028,197 (GRCm39) |
|
probably null |
Het |
Ddo |
G |
A |
10: 40,513,360 (GRCm39) |
V101I |
probably benign |
Het |
Disp2 |
T |
C |
2: 118,618,032 (GRCm39) |
|
probably benign |
Het |
Dnmt3b |
A |
C |
2: 153,516,297 (GRCm39) |
Y474S |
probably damaging |
Het |
Dpp6 |
T |
A |
5: 27,839,554 (GRCm39) |
N298K |
possibly damaging |
Het |
Fbf1 |
C |
T |
11: 116,037,339 (GRCm39) |
E940K |
probably damaging |
Het |
Fgd6 |
A |
G |
10: 93,881,501 (GRCm39) |
|
probably benign |
Het |
H2-M10.2 |
T |
C |
17: 36,595,568 (GRCm39) |
R241G |
probably damaging |
Het |
Haghl |
A |
T |
17: 26,002,072 (GRCm39) |
F207Y |
possibly damaging |
Het |
Helt |
G |
A |
8: 46,745,620 (GRCm39) |
R88C |
probably damaging |
Het |
Igf2bp2 |
T |
C |
16: 21,981,635 (GRCm39) |
K27E |
probably benign |
Het |
Il1b |
T |
C |
2: 129,207,022 (GRCm39) |
H246R |
probably benign |
Het |
Itprid1 |
T |
C |
6: 55,851,339 (GRCm39) |
|
probably null |
Het |
Kcnu1 |
C |
T |
8: 26,411,556 (GRCm39) |
S167L |
probably damaging |
Het |
Kif16b |
A |
T |
2: 142,544,534 (GRCm39) |
|
probably benign |
Het |
Myh7 |
A |
T |
14: 55,230,276 (GRCm39) |
S19T |
probably benign |
Het |
Ncaph2 |
T |
C |
15: 89,248,447 (GRCm39) |
|
probably null |
Het |
Nlrp4c |
T |
C |
7: 6,101,951 (GRCm39) |
L879P |
probably damaging |
Het |
Nqo2 |
T |
A |
13: 34,156,344 (GRCm39) |
N19K |
probably damaging |
Het |
Or2r2 |
C |
T |
6: 42,463,540 (GRCm39) |
V196M |
probably damaging |
Het |
Osbpl1a |
C |
A |
18: 12,952,635 (GRCm39) |
G93* |
probably null |
Het |
Pdxdc1 |
A |
G |
16: 13,661,659 (GRCm39) |
F459L |
possibly damaging |
Het |
Phc2 |
A |
T |
4: 128,601,809 (GRCm39) |
H88L |
probably damaging |
Het |
Pkd1l2 |
G |
A |
8: 117,792,484 (GRCm39) |
T436I |
probably benign |
Het |
Ptchd4 |
A |
T |
17: 42,813,340 (GRCm39) |
T414S |
possibly damaging |
Het |
Rab7b |
A |
G |
1: 131,626,280 (GRCm39) |
R103G |
probably damaging |
Het |
Retnla |
A |
G |
16: 48,662,943 (GRCm39) |
Y3C |
probably benign |
Het |
Samd7 |
G |
A |
3: 30,810,322 (GRCm39) |
R113H |
probably damaging |
Het |
Shisa9 |
G |
A |
16: 11,814,907 (GRCm39) |
|
probably benign |
Het |
Soat1 |
A |
T |
1: 156,268,926 (GRCm39) |
I208N |
possibly damaging |
Het |
Stab1 |
C |
A |
14: 30,872,100 (GRCm39) |
|
probably null |
Het |
Ube2v2 |
A |
G |
16: 15,374,349 (GRCm39) |
V77A |
probably benign |
Het |
Ubr5 |
T |
C |
15: 37,998,620 (GRCm39) |
E1617G |
probably damaging |
Het |
Vmn2r16 |
T |
A |
5: 109,508,757 (GRCm39) |
I495K |
possibly damaging |
Het |
Vwce |
G |
T |
19: 10,623,943 (GRCm39) |
R278L |
possibly damaging |
Het |
Wdr26 |
C |
T |
1: 181,010,349 (GRCm39) |
A551T |
probably damaging |
Het |
Wee1 |
A |
G |
7: 109,725,269 (GRCm39) |
I304V |
probably benign |
Het |
Xrcc5 |
C |
T |
1: 72,385,396 (GRCm39) |
H496Y |
possibly damaging |
Het |
Zfp142 |
G |
T |
1: 74,611,142 (GRCm39) |
S884R |
probably damaging |
Het |
|
Other mutations in Tti2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02005:Tti2
|
APN |
8 |
31,645,858 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02118:Tti2
|
APN |
8 |
31,645,537 (GRCm39) |
splice site |
probably null |
|
IGL02640:Tti2
|
APN |
8 |
31,645,942 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4366001:Tti2
|
UTSW |
8 |
31,641,224 (GRCm39) |
missense |
probably benign |
0.00 |
R2062:Tti2
|
UTSW |
8 |
31,644,338 (GRCm39) |
splice site |
probably benign |
|
R2081:Tti2
|
UTSW |
8 |
31,641,337 (GRCm39) |
missense |
possibly damaging |
0.46 |
R2089:Tti2
|
UTSW |
8 |
31,644,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R2091:Tti2
|
UTSW |
8 |
31,644,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R2091:Tti2
|
UTSW |
8 |
31,644,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R2301:Tti2
|
UTSW |
8 |
31,645,823 (GRCm39) |
missense |
probably benign |
0.03 |
R3735:Tti2
|
UTSW |
8 |
31,645,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R3875:Tti2
|
UTSW |
8 |
31,641,175 (GRCm39) |
missense |
probably benign |
|
R3916:Tti2
|
UTSW |
8 |
31,643,547 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3917:Tti2
|
UTSW |
8 |
31,643,547 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4827:Tti2
|
UTSW |
8 |
31,640,998 (GRCm39) |
missense |
probably benign |
0.06 |
R6522:Tti2
|
UTSW |
8 |
31,643,631 (GRCm39) |
missense |
probably null |
0.01 |
R6969:Tti2
|
UTSW |
8 |
31,644,329 (GRCm39) |
missense |
possibly damaging |
0.50 |
R9036:Tti2
|
UTSW |
8 |
31,645,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R9255:Tti2
|
UTSW |
8 |
31,645,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R9295:Tti2
|
UTSW |
8 |
31,643,550 (GRCm39) |
nonsense |
probably null |
|
R9688:Tti2
|
UTSW |
8 |
31,644,279 (GRCm39) |
missense |
probably damaging |
1.00 |
R9774:Tti2
|
UTSW |
8 |
31,645,660 (GRCm39) |
missense |
probably damaging |
1.00 |
X0004:Tti2
|
UTSW |
8 |
31,645,899 (GRCm39) |
frame shift |
probably null |
|
|